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Archive for the ‘Longevity’ Category

City of Fort Lauderdale, FL : Home

Thursday, August 4th, 2016

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The mission of the Fort Lauderdale City Commission is to represent the public interest; promote quick and courteous response to neighbor concerns; provide leadership and direction for the City's future; and assure Fort Lauderdale's present and future fiscal integrity.

The City of Fort Lauderdale is committed to providing quality service around the clock. Neighbors can use Lauderserv to submit a customer service request, pay a parking citation or utility bill, and access useful information. Use the portal on our website, download the smartphone app, or call us to request a new garbage cart, report a street light outage, inquire about volunteer opportunities, and more! Newfeatures allow you to pay your water bill or a parking citation right from your smartphone!

The City has developed a Vision Plan, the heart of which is our 2035 Vision Statement. Our Vision Statement is an inspirational view of the future and what our community wants to become. We invite you to journey with us to the Fort Lauderdale of 2035, as envisioned by you, our neighbors.

Press Play Fort Lauderdale, the Citys 2018 Strategic Plan, connects the dots between the communitys long-term Vision and the Citys day-to-day operations. It is the roadmap we will follow as we work to transform Fort Lauderdale into The City You Never Want to Leave.

The City of Fort Lauderdale is a close-knit community. You can help us enhance the overall quality of life by sharing your ideas with us. If you have a comment or suggestion about a City service, program, or event,we encourage you to share your input and help us build an even better community.

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1Vigor – Natural Health, Peak Performance, Lifestyle …

Thursday, August 4th, 2016

How Sleeping Naked Improves Men's Health Ralph Teller, Ironman Triathlete

Guys . . . . sleeping naked not only feels awesome it's great for your health! Sleeping naked improves sleep, metabolism, blood circulation, skin health, hormone secretion, relationships and sexual function Here's how sleeping naked improves men's . . . Read more

Distance Open Water Swimming Tips Trent Grimsey, English Channel World Record Holder - 6:55 hours

"Dedication is what you do when no one else is watching." Here are some tips to help you become a good distance open water swimmer! Find a program you enjoy: Swimming is like anything the more you practice, the better youll be. This is why . . . Read more

Organic Foods - For Improved Human Health and Environment Katie McKenna, LMHC CN

Research shows organic foods have more 25% more vitamins, minerals and phytonutrients because the top soil is better cared for and protected. Organic foods contain higher levels of beta carotene, vitamins C, D and E, cancer-fighting antioxidants . . .Read more

Key Nutrients for Red Blood Cell Production Ralph Teller, Ironman Triathlete

As red blood cells are the vehicle that delivers oxygen to our cells, sufficient production of red blood cells is necessary for good health and essential for athletic peak performance. Through lifestyle and good diet we can. . . . Read more

Doing the Math for Open Water Swim Racing Eney Jones, Pool and Open Water Champion

It is no surprise then that some of the greatest open water swimmers are some of the most intelligent people you will ever meet, examples are, Eva Fabian (Yale student) Alex Meyer (Harvard graduate) Alex Kostich (Stanford graduate). As Seneca, the Greek . . . Read more

Choosing Your Next Running Shoes Chris Harig, Duathlon National Champion

You've decided you are going to start a running program or its at least time to update your running shoes. Those with the luxury of a specialty running shop in the neighborhood are likely to come away from the experience without a scratch. Read more

Nine Golden Rules of Cycling Training Chris Baldwin, Professional Cyclist, Cycling and Triathlon Coach

My thirst for the science of performance in my career grew as I slowly climbed the ladder of professional cycling. I gathered information from any literature I could find and, more importantly, through questioning some of the best cyclists and coaches in . . . . . Read more

Running Strategy - 'Hitting the Wall' or Not Matt Bixley, Adventure and Distance Runner, New Zealand

Running strategies to avoid 'Hitting the Wall', include physical and mental preparedness, consistency, glycogen stores, nutrition and hydration, setting a pace strategy consistent with the level of strength and efficiency of your. . .Read more

25 Most Hydrating Natural Foods Ralph Teller, Ironman Triathlete

Scientists at the University of Aberdeen, England found the combination of salts, minerals and natural sugars found in high water content fruits and vegetables can actually hydrate people more effectively than just water or sports drinks . . . . Read more

How to Train your Autonomic Nervous System for Peak Performance Eney Jones, Pool and Open Water Champion

As athletes we focus almost entirely on the somatic nervous system. (Voluntary muscles) but how do we train and why do we overlook our autonomic nervous system? The autonomic system carries out the functions below the conscious level (i.e. the heart . . . Read more

Probiotics in Milk Products Improve Brain Function Ralph Teller, Ironman Triathlete

Researchers found that the regular consumption of probiotic-containing yogurt showed altered activity of brain regions that control central processing of emotion and sensation. The potential is to discover how milk product probiotics . . . . Read more

Triathlon Race Day Swimming Tips Trent Grimsey, English Channel Record Holder

Here are some tips to help you have a great triathlon swim on race day! Start Position: For Elite swimmers, on the start line always position yourself directly beside the fastest swimmer in the field. Age Groupers should position themselves . . . Read more

A Pool and Dryland Workout to Improve Open Water Swim Speed Thomas Lurz, Olympic Silver Medal Winner

Thomas Lurz is one of the world's best distance open water swimmers and won the Silver medal at the 2012 London Olympic Games 10k Open Water Marathon Swim. 1Vigor interviewed Thomas on the topic of pool swim workouts to improve . . . . Read more

Injury Recovery: Psychological, Emotional and Structural Healing Ezequiel Morales, Professional Triathlete, Argentina

We should take into account all aspects of healing including the psychological and emotional side of the athlete, in addition to the structural nature of the injury. For best healing results relating to the structural part of the injury input . . . Read more

Athlete Strategies to Maintain Healthy Joints Ralph Teller

For athletes, joint pain can interfere with training, race day performance and the ability to compete. Maintaining joint health is not only important for short term training and racing objectives, but also significant for long term health and longevity. . . . Read more

Cold Water Distance Swimming - How to Acclimate to Cold Water Ryan Stramrood, Distance Adventure Swimmer

So how does one prepare for and build tolerance for a cold water swim, an extreme cold swim or even an ice swim? The Cold: The starting point is to know that the water will bring your core temperature down to its level. So, the fitter you. . . Read more

Top 10 Running Tips for Triathlon and Running Training Lora Heyl Erickson, Ironman Triathlete and Coach

There are so many great running tips that I have learned over the last 26 years that I have run and coached running and triathlons, but these are some of the most valuable: Tip #1 - Be Cautious, Tip #2 - Rest, Tip #3 - Warm Up . . . Read more

Get Out of the Road! Trail Running Chris Harig, Duathlon National Champion

Get out of the road! Trail running for improved performance, injury prevention and mental health. About three years ago I made a fundamental switch in my running routine and started training almost entirely on trails. Part of the change ... Read more

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Oldest people – Wikipedia, the free encyclopedia

Thursday, August 4th, 2016

According to this criterion, the longest human lifespan is that of Jeanne Calment of France (18751997), who lived to the age of 122 years, 164 days. She met Vincent van Gogh when she was 12 or 13.[1] She received news media attention in 1985, after turning 110. Subsequent investigation found documentation for Calment's age, beyond any reasonable question, in the records of her native city, Arles, France.[2] More evidence of Calment's lifespan has been produced than for any other supercentenarian; her case serves as an archetype in the methodology for verifying the ages of the world's oldest people.[3]

As women live longer than men on average, combined records for both sexes are dominated by women. The longest undisputed lifespan for a man is that of Jiroemon Kimura of Japan (18972013), who died at age 116 years, 54 days.

Since the death of 116-year-old Jeralean Talley of the United States on 17 June 2015, Susannah Mushatt Jones, also of the United States, born 6 July 1899, is the oldest living person in the world whose age has been documented. Since the death of 112-year-old Yasutaro Koide of Japan on 19 January 2016, Yisrael Kristal of Israel, born 15 September 1903, is the world's oldest living man.

Systematic verification of longevity has only been practiced in recent decades and only in certain parts of the world.

Deceased Living ^ denotes age at death, or, if living, age as of 27 March 2016

Currently, all ten of the verified oldest people ever are women, thus a listing of the ten verified oldest women ever would be identical to the list above.

a^ Brown was born in Jamaica, then a British colony. b^ Gaudette was born in the United States.

The following is a list of men known to be over 110. However, only one of these people, Yisrael Kristal, is verified by the GRG.

a^ Kristal was born in Poland, then a part of the Russian Empire. b^ Castro was born in Peru.

This list is copied from the Gerontology Research Group's list of the World's Oldest Person Titleholders.[26] As the oldest living person is usually a female, a sequence of oldest females would be nearly redundant to this list. A sequence of oldest living men follows this sequence.

This list is copied from the Gerontology Research Group's list of the World's Oldest Man Titleholders.[13]

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The scientific quest to cure aging – CBS News

Thursday, August 4th, 2016

It's a pursuit that seems more like the plot of a science fiction movie than an actual goal of serious researchers around the world. But a number of scientists are fiercely working toward what was once only attainable in fables and fairy tales: they want to end aging.

The quest has even inspired a competition with a monetary prize from that hub of innovation, Silicon Valley. The Palo Alto Longevity Prize, founded by Dr. Joon Yun, a radiologist who heads Palo Alto Investors, is offering $1 million in prize money as a way to urge researchers figure out how to "hack the code" of aging.

While those in the growing field of longevity research admit the task at hand is expansive and complex, they say big advancements have already been made and expect to see more in the near future.

"The goal is similar to all medical research which is to make people healthier and keep people alive longer so we can have more productive lives and not be such a burden to society," David Sinclair, Ph.D., a professor of genetics and co-director of the Paul F. Glenn Center for the Biology of Aging at the Harvard Medical School, told CBS News.

The Australian-born biologist, who sits on the board of the Palo Alto Longevity Prize, discovered in 2013 that Nicotinamide adenine dinucleotide (NAD), a chemical found in every living organism, can turn on defenses against aging, though its levels decrease the older we grow.

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Atlantic Magazine contributing editor Gregg Easterbrook joins "CBS This Morning: Saturday" to discuss the consequences of rising longevity as ave...

Sinclair envisions a time -- maybe not too far away -- when doctors will prescribe medicine utilizing these findings to curb aging.

"We are finding genes and molecules that we can take as a pill that would slow down every disease from Alzheimer's to diabetes to cancer plus give us more energy during our whole lives," he said. "Side effects would be living longer, but the ultimate goal is there will be a future -- maybe it's only a decade or two away -- where people won't have to worry about getting these diseases in their 60s or 70s but can put that off to 100 or 110."

The Palo Alto Prize is meant to inspire and reward such innovations. The competition was announced in 2014 and final registration closed this past December. Winning research teams in two different categories -- who will be awarded $500,000 each -- are expected to be announced by the end of 2019.

The roughly 30 teams that are participating in the competition are taking a broad range of approaches, from stem cell therapies to gene modification to hormonal treatments to behavioral and nutritional interventions. Because of the nature of the competition, specifics about each project have not been disclosed to the public, but videos are available on the contest's website with teams introducing their research.

Quality versus quantity

Yun is quick to point out that the aim of most of longevity research -- and the ultimate goal of the Palo Alto competition -- is not simply to extend life in terms of sheer number of years lived, but to enhance quality of life, as well. He explains this in terms of homeostatic capacity, which refers to the body's natural ability to fight off stressors in order to remain healthy.

"Homeostatic capacity is probably nature's greatest gift. It's our ability to self-tune in response to stressors," he told CBS News. "It is so pervasively effective that we don't even realize we have it until we start losing it."

Yun went on to explain that when we're young and healthy, we don't even notice it. "That is the true definition of health," he said. "When you're feeling healthy, you're feeling nothing because you're in homeostasis. That's very different from what marketers try to say, that healthy means vitality and energy."

Then, after about the age of 40, our homeostatic capacity starts to decline. "We're more vulnerable to the forces of aging. All of a sudden you're finding that your body can't get back to homeostasis on its own," Yun said. "It's hard to ride roller coasters. It's hard to recover from injuries, from a late night, from jet lag. Foods we may have once loved, we are no longer able to tolerate. All of this happens at once, and these are all things everyone can feel. But think of all the things you can't feel."

He gave the example that when people are young and healthy and their blood pressure or sugar level is high, the body brings itself back to homeostasis on its own. But as we age, the body loses this ability.

"We give these things names like diabetes and hypertension," he said. "But maybe it's all really the same process that is the decline of homeostatic capacity."

When asked why he set up the competition to find ways to solve these problems of aging, rather than invest the money directly into research, Yun said he thinks the nature of a contest yields the best results.

"What's wonderful about prizes is that you set a goal and you're essentially inviting a diversity of options to compete and see which one wins," he said. "It's very much like how nature and evolution work."

"What is it that you're living for?"

But not everyone thinks the quest to cure aging is well-founded or wise. Several prominent bioethicists have spoken out against such efforts to extend longevity.

Dr. Ezekiel Emanuel, an oncologist and Chair of the Department of Medical Ethics and Health Policy at the University of Pennsylvania, is among them. In 2014, Emanuel penned a controversial article for the Atlantic titled "Why I Hope to Die at 75."

"I think it's fascinating that so many people are obsessed with living long," he told CBS News. "If you ask most people about quality versus quantity of life, they will say in a second that quality is what's really important. And then you probe and you find that people are so psychologically scared of dying and not having lived out a meaningful life. But when you talk to older people, many of them are sort of tired of life. They've lost friends and loved ones or activities are restricted and maybe it's not so great after all."

For Emanuel, such frank discussions with older adults and time spent in self-reflection led him to the decision that he does not aspire to an exceptionally long life and would not take steps to extend it.

In the Atlantic article, Emanuel, who is in good health in his late 50s, made clear that he is not looking to end his life through suicide or euthanasia. Rather, at 75, he believes he will be content enough with his life to not actively try to prolong it. "I think this manic desperation to endlessly extend life is misguided and potentially destructive," he wrote.

"The real issue is what makes a meaningful life," he told CBS News. "Is it living as long as you can or is there something else going on? If you ask me, it's the something else we really ought to care about. What is it that you're living for?"

When asked about the views expressed by longevity researchers that their work focuses not just on extending years lived, but on increasing quality of life, Emanuel answered with plenty of skepticism.

"How are you going to cure all of the causes of death?" he asked. "That's kind of a way for scientists to rationalize what they're doing. I can understand that it's an interesting puzzle to solve and many people are passionate about it, but I don't think it's something we ought to be doing."

Of course, longevity researchers vehemently disagree and say such objections are misguided.

"What we're talking about is being able to prevent and treat the major diseases of society," Sinclair said. "Cancer at one point in human history was totally natural. Heart disease was unavoidable. Nobody now would say, 'Oh, cancer is natural and we shouldn't work on it.' We use our technology to lead better lives and make the world a better place and improve the human condition and that's what we're aiming to do here."

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List of countries by life expectancy – Wikipedia, the free …

Thursday, August 4th, 2016

This is a collection of lists of countries by life expectancy at birth.

Life expectancy equals the average number of years a person born in a given country would live if mortality rates at each age were to remain constant in the future. The life expectancy is shown separately for males and females, as well as a combined figure. Several non-sovereign entities are also included in this list.

The figures reflect the quality of healthcare in the countries listed as well as other factors including ongoing wars, obesity, and HIV infections.[citation needed]

Worldwide, the average life expectancy at birth was 71.0 years (68.5 years for males and 73.5 years for females) over the period 20102013 according to United Nations World Population Prospects 2012 Revision,[3] or 70.7 years (68.2 years for males and 73.2 years for females) for 2009 according to The World Factbook.[4] According to the World Health Organization (WHO), women on average live longer than men in all countries, except in Tonga.

The countries with the lowest overall life expectancies per the WHO are Sierra Leone, the Central African Republic, the Democratic Republic of the Congo, Guinea-Bissau, Lesotho, Somalia, Swaziland, Angola, Chad, Mali, Burundi, Cameroon, and Mozambique. Of those countries, only Lesotho, Swaziland, and Mozambique in 2011 were suffering from an HIV prevalence rate of greater than 10 percent in the 1549 age group.[5]

Comparing life expectancies from birth across countries can be problematic. There are differing definitions of live birth vs stillbirth even among more developed countries and less developed countries often have poor reporting.[6]

Data published in 2015.[7] (Retrieved on 11 February 2016)

On July 2014, the Population Division of the United Nations Department of Economic and Social Affairs (UN DESA), released World Population Prospects, The 2015 Revision.[3] The following table shows the life expectancy at birth for the period 2010 to 2015.

over 80

77.5-80.0

75.0-77.5

72.5-75.0

70.0-72.5

67.5-70.0

65.0-67.5

60-65

55-60

50-55

45-50

under 45

not available

The Global Burden of Disease 2010 study published updated figures in 2012,[8] including recalculations of life expectancies[9] which differ substantially in places from the UN estimates for 2010 (reasons for this are discussed in the freely available appendix to the paper, pages 2527, currently not available). Although no estimate is given for the sexes combined, for the first time life expectancy estimates have included uncertainty intervals.

>80

>77.5

>75

>72.5

>70

>67.5

>65

>60

>55

>50

>45

>40

<40

The US CIA published the following life expectancy data in its annual world factbook 2012.[1]

Figures are from the CIA World Factbook 2009[1] and from the 2010 revision of the United Nations World Population Prospects report, for 20052010,[3] (data viewable at http://esa.un.org/wpp/Sorting-Tables/tab-sorting_mortality.htm, with equivalent spreadsheets here, here, and here).

Only countries/territories with a population of 100,000 or more in 2010 are included in the United Nations list. WHO database 2013 http://www.who.int/gho/publications/world_health_statistics/EN_WHS2013_Full.pdf

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Welcome to Princeton Longevity

Thursday, August 4th, 2016

Welcome to the future of Preventive Medicine

Princeton Longevity Center is a next-generation preventive medical facility providing one of the most advanced, integrated and individually tailored programs in the country. With focus on early disease detection and evaluating and modifying risk for future disease, Princeton Longevity Centers unique program gives you the ability to take control of your future health before the onset of symptoms or other indications of a problem.

Princeton Longevity Centers Comprehensive Preventive Exams combine the newest and most advanced technology with the most in-depth assessment available to detect potential health problems. Our preventive medicine experts will show you simple, easy adjustments you can make that wont dramatically impact your lifestyle but will give you the tools you need to maximize your future health and keep you looking and feeling years younger. Our individually tailored programs will improve your health and longevity, enabling you to make the most of your future years for you and the people who depend on you.

Named one of the countrys top centers for a Comprehensive or Executive Physical exam by the Wall Street Journal and Forbes Magazine, the Princeton Longevity Center provides you with an unparalleled level of personal care and attention.

When you visit Princeton Longevity Center, youll be met by a team of professionals that provides an extensive series of medical assessments, diagnostic tests and health screenings. On the same day well review all your results with you and give you as much time as you need to ask questions about them. Individualized attention from a team of Physicians, Exercise Physiologists, Registered Dietitians, Nurses and Patient Care Coordinators is a hallmark of our preventive medicine center, and sets us apart from other wellness centers. Patients come to Princeton Longevity Center because were not a hospital-based exam we are the specialist in prevention and early disease detection.

You will find that one day with Princeton Longevity Center will provide more insight into your health and future health than all your previous routine annual exams combined.

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Weight Loss Moore, Norman, South OKC OK | Longevity

Thursday, August 4th, 2016

Have enjoyed working with Kristen over the last 5 weeks! I have lost 16.6 pounds so far and am looking forward to what else I have to lose with the assistance of the Longevity crew!-Longevity Client

At Longevity, Medical Director Dr. Darryl Robinson offers the premier Medically Supervised Weight Loss Program in Oklahoma City. Through this comprehensive lifestyle management program we offer a unique approach on patient coaching. In a positive manner, we identify and address the issues that contribute to unhealthy weight gain and encourage a healthy lifestyle transition. All this comes together to eliminate the excess weight and keep it off.

Our program includes nutritional products and counseling to help improve weight control, diabetes, high blood pressure and high cholesterol, reduce hunger, lessen cravings, increase energy and overall outlook, maintain lean muscle mass and focus on permanent lifestyle change.

An initial consultation is needed to determine which weight loss program is right for you. The initial consultation includes:

Call Longevity at 405-703-4990 to schedule your Medically Supervised Weight Loss Program consultation or click here to contact us.

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Ray Peat, PhD on Carbon Dioxide, Longevity, and …

Thursday, August 4th, 2016

Also see: Protective Altitude Protect the Mitochondria Lactate Paradox: High Altitude and Exercise Altitude Improves T3 LevelsProtective Carbon Dioxide, Exercise, and PerformanceSynergistic Effect of Creatine and Baking Soda on Performance Altitude Improves T3 Levels Altitude Sickness: Therapeutic Effects of Acetazolamide and Carbon Dioxide Comparison: Carbon Dioxide v. Lactic Acid Carbon Dioxide Basics Universal Principle of Cellular Energy Carbon Dioxide as an Antioxidant Comparison: Oxidative Metabolism v. Glycolytic Metabolic

Over the oxygen supply of the body carbon dioxide spreads its protecting wings. Friedrich Miescher, Swiss physiologist, 1885

===========

People who live at very high altitudes live significantly longer; they have a lower incidence of cancer (Weinberg, et al., 1987) and heart disease (Mortimer, et al., 1977), and other degenerative conditions, than people who live near sea level. As I have written earlier, I think the lower energy transfer from cosmic radiation is likely to be a factor in their longevity, but several kinds of evidence indicate that it is the lower oxygen pressure itself that makes the biggest contribution to their longevity.

The end product of respiration is carbon dioxide, and it is an essential component of the life process. The ability to produce and retain enough carbon dioxide is as important for longevity as the ability to conserve enough heat to allow chemical reactions to occur as needed.

Carbon dioxide protects cells in many ways. By bonding to amino groups, it can inhibit the glycation of proteins during oxidative stress, and it can limit the formation of free radicals in the blood; inhibition of xanthine oxidase is one mechanism (Shibata, et al., 1998). It can reduce inflammation caused by endotoxin/LPS, by lowering the formation of tumor necrosis factor, IL-8 and other promoters of inflammation (Shimotakahara, et al., 2008). It protects mitochondria (Lavani, et al., 2007), maintaining (or even increasing) their ability to respire during stress.

The replicative lifespan of a cell can be shortened by factors like resveratrol or estrogen that interfere with mitochondrial production of carbon dioxide. Both of those chemicals cause skin cells, keratinocytes, to stop dividing, to take up calcium, and to begin producing the horny material keratin, that allows superficial skin cells to form an effective barrier. This process normally occurs as these cells differentiate from the basal (stem) cells and, by multiplying, move farther outward away from the underlying blood vessels that provide the nutrients that are oxidized to form carbon dioxide, and as they get farther from the blood supply, they get closer to the external air, which contains less than 1% as much CO2 as the blood. This normally causes their eventual hardening into the keratin cells, but when conditions are optimal, numerous layers of moist, translucent cells that give the skin the characteristic appearance of youth, will be retained between the basal cells and the condensed surface layers. (Wilke, et al., 1988)

In other types of tissue, a high level of carbon dioxide has a similar stabilizing effect on cells, preserving stem cells, limiting stress and preventing loss of function. In the lining of the mouth, where the oxygen tension is lower, and carbon dioxide higher, the cells dont form as much keratin as the skin cells do. In the uterus, the lining cells would behave similarly, except that estrogen stimulates keratinization. A vitamin A deficiency mimics an estrogen excess, and can cause excessive keratinization of membrane cells.

Certain kinds of behavior, as well as nutrition and other environmental factors, increase the production and retention of carbon dioxide. The normal intrauterine level of carbon dioxide is high, and it can be increased or decreased by changes in the mothers physiology. The effects of carbon dioxide on many biological processes involving methylation and acetylation of the genetic material suggest that the concentration of carbon dioxide during gestation might regulate the degree to which parental imprinting will persist in the developing fetus. There is some evidence of increased demethylation associated with the low level of oxygen in the uterus (Wellman, et al., 2008). A high metabolic rate and production of carbon dioxide would increase the adaptability of the new organism, by decreasing the limiting genetic imprints.

Frogs and toads, being amphibians, are especially dependent on water, and in deserts or areas with a dry season they can survive a prolonged dry period by burrowing into mud or sand. Since they may be buried 10 or 11 inches below the surface, they are rarely found, and so havent been extensively studied. In species that live in the California desert, they have been known to survive 5 years of burial without rainfall, despite a moderately warm average temperature of their surroundings. One of their known adaptations is to produce a high level of urea, allowing them to osmotically absorb and retain water. (Very old people sometimes have extremely high urea and osmotic tension.)

Some laboratory studies show that as a toad burrows into mud, the amount of carbon dioxide in its tissues increases. Their skin normally functions like a lung, exchanging oxygen for carbon dioxide. If the toads nostrils are at the surface of the mud, as dormancy begins its breathing will gradually slow, increasing the carbon dioxide even more. Despite the increasing carbon dioxide, the pH is kept stable by an increase of bicarbonate (Boutilier, et al., 1979). A similar increase of bicarbonate has been observed in hibernating hamsters and doormice.

Thinking about the long dormancy of frogs reminded me of a newspaper story I read in the 1950s. Workers breaking up an old concrete structure found a dormant toad enclosed in the concrete, and it revived soon after being released. The concrete had been poured decades earlier.

Although systematic study of frogs or toads during their natural buried estivation has been very limited, there have been many reports of accidental discoveries that suggest that the dormant state might be extended indefinitely if conditions are favorable. Carbon dioxide has antioxidant effects, and many other stabilizing actions, including protection against hypoxia and the excitatory effects of intracellular calcium and inflammation (Baev, et al., 1978, 1995; Bari, et al., 1996; Brzecka, 2007; Kogan, et al., 1994; Malyshev, et al., 1995).

Bats have a very high metabolic rate, and an extremely long lifespan for an animal of their size. While most animals of their small size live only a few years, many bats live a few decades. Bat caves usually have slightly more carbon dioxide than the outside atmosphere, but they usually contain a large amount of ammonia, and bats maintain a high serum level of carbon dioxide, which protects them from the otherwise toxic effects of the ammonia.

The naked mole rat, another small animal with an extremely long lifespan (in captivity they have lived up to 30 years, 9 or 10 times longer than mice of the same size) has a low basal metabolic rate, but I think measurements made in laboratories might not represent their metabolic rate in their natural habitat. They live in burrows that are kept closed, so the percentage of oxygen is lower than in the outside air, and the percentage of carbon dioxide ranges from 0.2% to 5% (atmospheric CO2 is about 0.038). The temperature and humidity in their burrows can be extremely high, and to be very meaningful their metabolic rate would have to be measured when their body temperature is raised by the heat in the burrow.

Besides living in a closed space with a high carbon dioxide content, mole rats have another similarity to bees. In each colony, there is only one female that reproduces, the queen, and, like a queen bee, she is the largest individual in the colony. In beehives, the workers carefully regulate the carbon dioxide concentration, which varies from about 0.2% to 6%, similar to that of the mole rat colony. A high carbon dioxide content activates the ovaries of a queen bee, increasing her fertility.

Since queen bees and mole rats live in the dark, I think their high carbon dioxide compensates for the lack of light. (Both light and CO2 help to maintain oxidative metabolism and inhibit lactic acid formation.) Mole rats are believed to sleep very little. During the night, normal people tolerate more CO2, and so breathe less, especially near morning, with increased active dreaming sleep.

A mole rat has never been known to develop cancer. Their serum C-reactive protein is extremely low, indicating that they are resistant to inflammation. In humans and other animals that are susceptible to cancer, one of the genes that is likely to be silenced by stress, aging, and methylation is p53, a tumor-suppressor gene.

If the intrauterine experience, with low oxygen and high carbon dioxide, serves to reprogram cells to remove the accumulated effects of age and stress, and so to maximize the developmental potential of the new organism, a life thats lived with nearly those levels of oxygen and carbon dioxide might be able to avoid the progressive silencing of genes and loss of function that cause aging and degenerative diseases.

I think of high altitude as analogous to theprotected gestational state. (Both progesteroneand carbon dioxide are increased in peopleadapted to high altitude.) Respiratory acidosis,meaning the retention of carbon dioxide, is veryprotective, and is an outstanding feature of life inthe uterus. Even at the time that an embryo isimplanting in the uterus, adequate carbon dioxideis crucial. Many of the mysteries of embryologyand developmental biology have been explained by the presence of a high level of carbon dioxideduring gestation. For example, an injury to the fetus heals without scarring, that is, with completeregeneration instead of the formation of a sort ofcollagenous plug. Over the last fifty years, severalpeople have discovered that simply enclosing awound (for example an amputated finger tip) in anair-tight compartment allows remarkably complete regeneration, even in adults, who supposedly have lost the power of regeneration.(Exposure of tissues to air causes them to losecarbon dioxide.)

During gestation, after organs have differentiated,nerve cells extend their fibers from the brain to innervate muscles and other tissues. The specialconditions of life in the uterus support thisprocess, but something similar can happen duringadult life, when damaged nerves regenerate. Amajor difference between injury to the fetus, andinjury to an adult, is that the wound regeneratesperfectly without a scar in the fetus, but in theadult, regeneration is often impaired, and aconnective tissue scar replaces normally functioningtissue.

In childhood, wounds heal quickly, and inflammation is quickly resolved; in extreme old age, or during extreme stress or starvation, wound healing is much slower, and the nature of the inflammation and wound closure is different. In the fetus, healing can be regenerative and scarless, for example allowing a cleft palate to be surgically corrected without scars (Weinzweig, et al., 2002).

The amount of disorganized fibrous material formed in injured tissue is variable, and it depends on the state of the individual, and on the particular situation of the tissue. For example, the membranes lining the mouth, and the bones and bone marrow, and the thymus gland are able to regenerate without scarring. What they have in common with each other is a relatively high ratio of carbon dioxide to oxygen. Salamanders, which are able to regenerate legs, jaw, spinal cord, retina and parts of the brain (Winklemann & Winklemann, 1970), spend most of their time under cover in burrows, which besides preventing drying of their moist skin, keeps the ratio of carbon dioxide to oxygen fairly high.

The regeneration of finger tips, including a well-formed nail if some of the base remained, will occur if the wounded end of the finger is kept enclosed, for example by putting a metal or plastic tube over the finger. The humidity keeps the wound from forming a dry scab, and the cells near the surface will consume oxygen and produce carbon dioxide, keeping the ratio of carbon dioxide to oxygen much higher than in normal uninjured tissue.

Carbon dioxide is being used increasingly to prevent inflammation and edema. For example, it can be used to prevent adhesions during abdominal surgery, and to protect the lungs during mechanical ventilation. It inhibits the formation of inflammatory cytokines and prostaglandins (Peltekova, et al., 2010, Peng, et al., 2009, Persson & van den Linden, 2009), and reduces the leakiness of the intestine (Morisaki, et al., 2009). Some experiments show that as it decreases the production of some inflammatory materials by macrophages (TNF: Lang, et al., 2005), including lactate, it causes macrophages to activate phagocytic neutrophils, and to increase their number and activity (Billert, et al., 2003, Baev & Kuprava, 1997).

Factors that are associated with a decreased level of carbon dioxide, such as excess estrogen and lactate, promote fibrosis. Adaptation to living at high altitude, which is protective against degenerative disease, involves reduced lactate formation, and increased carbon dioxide. It has been suggested that keloid formation (over-growth of scar tissue) is less frequent at high altitudes (Ranganathan, 1961), though this hasnt been carefully studied. Putting an injured arm or leg into a bag of pure carbon dioxide reduces pain and accelerates healing.

In the fetus, especially before the fats from the mothers diet begin to accumulate, signals from injured tissue produce the changes that lead quickly to repair of the damage, but during subsequent life, similar signals produce incomplete repairs, and as they are ineffective they tend to be intensified and repeated, and eventually the faulty repair processes become the main problem. Although this is an ecological problem, it is possible to decrease the damage by avoiding the polyunsaturated fats and the many toxins that synergize with them, while increasing glucose, niacinamide, carbon dioxide, and other factors that support high energy metabolism, including adequate exposure to long wavelength light and avoidance of harmful radiation. As long as the toxic factors are present, increased amounts of protective factors such as progesterone, thyroid, sugar, niacinamide, and carbon dioxide can be used therapeutically and preventively.

For hundreds or thousands of years, the therapeutic value of carbonated mineral springs has been known. The belief that it was the waters lively gas content that made it therapeutic led Joseph Priestley to investigate ways to make artificially carbonated water, and in the process he discovered oxygen. Carbonated water had its medical vogue in the 19th century, but the modern medical establishment has chosen to define itself in a way that glorifies dangerous, powerful treatments, and ridicules natural and mild approaches. The motivation is obviousto maintain a monopoly, there must be some reason to exclude the general public from the practice of medicine. Witch doctors maintained their monopoly by working with frightening ghost-powers, and modern medicine uses its technical mystifications to the same purpose.vAlthough the medical profession hasnt lost its legal monopoly on health care, corporate interests have come to control the way medicine is practiced, and the way research is done in all the fields related to medicine.

I have been using aging (menopause and the ovaries) and cancer (carbon monoxide as a hormone of cellular immortality) to explore the issue of cell renewal and tissue regeneration. Yesterday, Lita Lee sent me an article about K. P. Buteyko, describing his approach to the role of carbon dioxide in physiology and medicine. Buteyko devoted his career to showing that sufficient carbon dioxide is important in preventing an exaggerated and maladaptive stress response. He advocated training in intentional regulation of respiration (avoiding habitual hyperventilation) to improve oxygenation of the tissues by retaining carbon dioxide. He showed that a deficiency of carbon dioxide (such as can be produced by hyperventilation, or by the presence of lactic acid in the blood) decreases cellular energy (as ATP and creatine phosphate) and interferes with the synthesis of proteins (including antibodies) and other cellular materials.

When I first heard of Buteykos ideas, I saw the systemic importance of carbon dioxide, but I wasnt much impressed by his idea of intentionally breathing less. If the hyperventilation is produced by anxiety, then a deliberate focussing on respiration can help to quiet the nerves. Knowing that hyperventilation can make a person faint, because loss of carbon dioxide causes blood vessels in the brain to constrict, I saw that additional carbon dioxide would increase circulation to the brain. This seemed like a neat system for directing the blood supply to the part of the brain that was more active, since that would be the part producing the most carbon dioxide.

In a nutrition class, in the late 70s, I described the way metabolically produced carbon dioxide opens blood vessels in the brain, and mentioned that carbonated water, or soda water, should improve circulation to the brain when the brains production of carbon dioxide wasnt adequate. A week later, a student said she had gone home that night and (interpreting soda water as bicarbonate of soda in water) given her stroke-paralyzed mother a glass of water with a spoonful of baking soda in it. Her mother had been hemiplegic for 6 months following a stroke, but 15 minutes after drinking the bicarbonate, the paralysis lifted, and she remained normal. Later, a man who had stroke-like symptoms when he drank alcohol late at night, found that drinking a glass of carbonated water caused the symptoms to stop within a few minutes.

Realizing that low thyroid people produce little carbon dioxide, it seemed to me that there might be a point at which the circulatory shut-down of unstimulated parts of the brain would become self-sustaining, with less circulation to an area decreasing the CO2 produced in that area, which would cause further vasoconstriction. Carbon dioxide (breathing in a bag, or drinking carbonated water, or bathing in water with baking soda) followed by thyroid supplementation, would be the appropriate therapy for this type of functional ischemia of the brain.

I have been concerned about the probable effects on the fetus of the silly panting respiration that is being taught to so many pregnant women, to use during labor. Panting blows out so much carbon dioxide that it causes vasoconstriction. Possibly the uterus is protected against this, and possibly the fetus produces enough carbon dioxide that it is protected, but this isnt known. Especially if the mother is hypothyroid, it seems that this could interfere with the delivery of oxygen to the fetus. Besides vasoconstriction, Buteyko points out that the Bohr effect, in which CO2 causes hemoglobin to release oxygen, means that a low level of carbon dioxide decreases the availability of oxygen. If the Bohr effect applies to fetal hemoglobin, then this suggests that the mothers panting will deprive the fetal tissues of oxygen.

It is normal for the fetus to be exposed to a high concentration of carbon dioxide. Recent experiments with week-old rats show that carbon dioxide, at the very high concentration of 6% powerfully protects against the brain damage caused by oxygen deprivation (tying a carotid artery and administering 8% oxygen). (R. C. Vannucci, et al., 1995.)

In general, lactic acid in the blood can be takenas a sign of defective respiration, since the breakdownof glucose to lactic acid increases to makeup for deficient oxidative energy production. Normalaging seems to involve a tendency toward excesslactic acid -production, and age-pigment isknown to activate the process. Eliminating respiratorytoxins (such as unsaturated oils, estrogenicand antithyroid substances, lead, and excess iron)is the most obvious first step to take when there isexcess lactic acid formation. Carbon dioxide supplementshave been shown experimentally to reduceresidual lactate production. Many peopleexperience exhilaration when they go to very highaltitudes, and it is known that people generallybum calories faster at high altitude. It has beenfound that, during intense exercise (which alwaysproduces a lactic acid accumulation inthe blood), a lower peak accumulation of lactate occurs at high altitude, and this seems tobe caused by a reduction in the rate of glycolysis,or glucose consumption. (B.Grassi, et aI.)Since there is less oxygen at high elevation, andsince oxygen is used to consume lactic acid, thiseffect is the opposite of what many people expected.In some sense, respiration becomes moreefficient at high altitude. Youth and increased times supported the process by helping to stabilize the high energy metabolism of the brain, and evenby stabilizing the energized state of water thatsupports brain efficiency. Roman Schmitt has proposedthat, 66 million years ago when dinosaursbecame extinct and mammals began their rapidevolution, at that time hydrothermal venting wentwild, releasing huge volumes of carbon dioxideand other substances into the atmosphere.

Antarctic ice cores show there were large increasesin atmospheric carbon dioxide in relativelyrecent times: 10,200, 11,600, and 12,900 yearsago, and two broad peaks in carbon dioxide releaseoccurred just 4,200 and 7,700 years ago(Figge and White.) Local or regional increases incarbon dioxide from volcanism could have morecontinuous effects on brain development.

In times of lower atmospheric carbon dioxide,our Krebs cycle still produces it internally, and therapid development of the brain during gestationtakes advantage of the high concentration of carbon dioxide in the uterus.(These ideas make me doubt the safety of the rapid breathing encouragedby some obstetricians.)

We know that glucose can be metabolized into pyruvic acid, which, in the presence of oxygen, can be metabolized into carbon dioxide. Without oxygen, pyruvic acid can be converted into lactic acid. The production of lactic acid tends to increase the pH inside the cell, and its excretion can lower the pH outside the cell.

The decrease of carbon dioxide that generally accompanies increased lactic acid, corresponds to increased intracellular pH. Carbon dioxide binds to many types of protein, for example by forming carbamino groups, changing the protein conformation, as well as its electrical properties, such as its isoelectric point. With increased pH, cell proteins become more strongly ionized, tending to separate, allowing water to enter the spaces, in the same way a gel swells in an alkaline solution.

The Bohr-Haldane effect describes the fact that hemoglobin releases oxygen in the presence of carbon dioxide, and releases carbon dioxide in the presence of oxygen. When oxygen is too abundant, it makes breathing more difficult, and one of its effects is to cause carbon dioxide to be lost rapidly. At high altitude, more carbon dioxide is retained, and this makes cellular respiration more efficient.

The importance of carbon dioxide to cell control process, and to the structure of the cell and the structure of proteins in general suggested that degenerative diseases would be less common at high altitude. Wounds and broken bones heal faster at high altitude, but the available statistics are especially impressive in two of the major degenerative conditions, cancer and cataracts.

The two biggest studies of altitude and cataracts (involving 12,217 patients in one study, and 30,565 lifelong residents in a national survey in Nepal) showed a negative correlation between altitude and the incidence of cataract. At high altitude, cataracts appeared at a later age. In Nepal, an increase of a few thousand feet in elevation decreased the incidence of cataracts by 2.7 times. At the same time, it was found that exposure to sunlight increased the incidence of cataracts, and since the intensity of ultraviolet radiation is increased with altitude, this makes the decreased incidence of cataracts even more important.

All of the typical causes of cataracts, aging, poisons, and radiation, decrease the formation of carbon dioxide, and tend to increase the formation of lactic acid. Lactic acid excess is typically found in eyes with cataracts.

The electrical charge on the structural proteins will tend to increase in the presence of lactic acid or the deficiency of carbon dioxide, and the increase of charge will tend to increase the absorption of water.

The lens can survive for a considerable length of time in vitro (since it has its own circulatory system), so it has been possible to demonstrate that changes in the composition of the fluid can cause opacities to form, or to disappear.

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Ray Peat, PhD on Carbon Dioxide, Longevity, and ...

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Princeton Longevity Center :: Staff Bios

Thursday, August 4th, 2016

PLC Staff Bios

David A. Fein, MD Internal Medicine Medical Director Locations: Princeton, Shelton, Fairfax

Founder of the Princeton Longevity Center, Dr. David Fein practiced general Internal Medicine in Morristown, NJ for 16 years. He has traveled extensively to research the latest medical advances to incorporate them into the Princeton Longevity Center. Dr Fein is a Founding Member of the Society for Cardiovascular CT. He lectures on topics in preventive medicine and the safe use of nutritional supplements. Dr. Fein has also been involved in developing health-related legislation in New Jersey.

Dr. Fein is on the Attending Staff at Morristown Memorial Hospital.

A graduate of Franklin & Marshall College in Lancaster, PA, Dr. Fein received his medical degree from New York University School of Medicine and was elected to the Alpha Omega Alpha Medical Honor Society. Dr. Fein completed his residency training at Bellevue Hospital- New York University Medical Center and is Board Certified in Internal Medicine.

John Rumberger , PhD, MD, FACC Cardiology Director of Cardiac Imaging Locations: Princeton

Dr. Rumberger is recognized as one of the world's leading authorities on cardiac and vascular imaging using CT Scanning. His notable credentials make him uniquely qualified to provide interpretation of Coronary CT Angiography.

Dr. Rumberger has been Professor of Medicine and Consultant in the Department of Cardiovascular Diseases at the Mayo Clinic in Rochester, Minnesota. It was during this time that his reputation as a leader in the development and application of computed tomography of the heart was established. He has published extensively and continues to lecture and train other physicians in the United States, Europe, and Asia.

Dr. Rumberger received his doctorate in engineering from The Ohio State University in 1976 and graduated from the University Of Miami School Of Medicine in 1978. He completed his internship and residency in internal medicine at The Ohio State University Hospitals, and completed a cardiovascular diseases fellowship and early faculty development at the University of Iowa. Dr. Rumberger is currently Director of Cardiac Imaging and Lipid Management at PLC and is Board Certified in Internal Medicine and Cardiovascular Diseases.

During his over 25 year career as a clinician, educator, and researcher, Dr. Rumberger has published nearly 500 scientific papers and book chapters. He has lectured worldwide on Cardiac CT, early disease diagnosis, and wellness. He is an Established Investigator of the American Heart Association and a Founding Member of the International Society of Atherosclerosis Imaging. Dr Rumberger is an active Reviewer for the Journal of the American Medical Association, Archives of Internal Medicine, publications of both the American Heart Association and American College of Cardiology, and the New England Journal of Medicine.

Charles Miner MD Internal Medicine Locations: Shelton

Dr. Miner is board-certified in Internal Medicine and has been in practice since 1982.

He is on the Board of Directors of The Stamford Hospital and the Stamford Hospital Foundation, on the medical staff of The Norwalk Hospital, and is on the Board of Directors of Misonix, Inc. He is listed in Castle Connolly Medical Ltd.s Top Doctors New York Metro Area and is an instructor in Clinical Medicine at Columbia University.

Dr. Miner performed his residency at Lenox Hill Hospital in New York, received his medical degree from the University of Cincinnati College of Medicine and holds a Bachelor of Science degree from Lehigh University.

Dr. Miner has particular expertise in personal services that emphasize prevention and screening, with a special interest in patient care during travel. He has developed a unique system that provides patients instant, secure access to their medical records via the web along with 24/7 access via cell phone, email or "BlackBerry" should a problem arise anywhere in the world. For physicians who wish to engage Dr. Miner's practice model, Dr. Miner has founded Lifestream MD, LLC, a physician-practice consulting company.

Dr. Miner serves as a member of the board of directors for Misonix, Inc., an ultrasonic medical device company based in Farmingdale, Long Island, and on the strategy and business development committee for Stamford Hospital. He previously served as director of web-based health and wellness

Oscar Ellison, III MD Internal Medicine Locations: Fairfax

Dr. Oscar Ellison, III, graduated from Harvard College and Georgetown University School of Medicine.

His focus has always been on personalized medical care, wellness and prevention. He has extensive experience treating hypertension, diabetes and hyperlipidemia.

Dr. Ellison has served on numerous boards, including the Arlington Hospital Physicians Organization and the Arlington County Medical Society. He has also served as Vice Chair/Chairman of the Virginia Hospital Center Department of Family Practice. Dr. Ellison is experienced in Phase 3 Clinical Research, and is the Medical Director of Atlantic Medical Associates.

Dr Ellison has been recognized as a Top Doctor by Washingtonian Magazine, Northern Virginia Magazine, and Washington Checkbook Magazine, and has been listed in the Leading Physicians of the World by the IAHCP. An accomplished athlete, Dr. Ellison competed in the Henley Royal Regatta and has won the Oxford triathlon.

Affiliated Medical Staff:

Yaakov Applbaum, MD Radiologist Medical Director and Acting Chairman Department of Radiology Capital Health System

Dr. Applbaum received his MD degree from the Albert Einstein College of Medicine. His esidency in Radiology at Maimonides Medical Center was followed by a fellowship in Interventional Radiology at the University of California at Irvine Medical Center. He previously served as Chief, Vascular and Interventional Radiology, at Staten Island University Hospital. He is board certified in Diagnostic Radiology, with Certificates of Added Qualification in both Interventional Radiology and Neuroradiology, by the American Board of Radiology (ABR.)

Ajay Choudhri, MD Radiologist, Vascular and Interventional Radiology Department of Radiology Capital Health System

Dr. Choudhri received his MD degree from the New Jersey Medical School, UMDNJ, Newark. His residency in Radiology at Albert Einstein College of Medicine, Montefiore Medical Center, was followed by a fellowship in Interventional Radiology at the Miami Cardiac and Vascular Institute. He previously served as Chief, Interventional Radiology at Jackson South Hospital in Miami. He is board certified in Radiology by the ABR.

Amin Chaoui, MD Radiologist The Center for Virtual Colonoscopy Boston Diagnostics

Dr. Amin Chaoui is an Associate radiologist at Faulkner/Brigham & Womens hospital, Department of Radiology, Harvard University School of Medicine. A graduate of the University of Geneva School of Medicine, Dr. Chaoui's graduate training included a research fellowship in Body Imaging at University of Florida College of Medicine and a Fellowship in Body Imaging at Boston Medical Center, Boston University School of Medicine. Dr. Chaoui is certified by the American Board of Radiology. From 1999-2002, he served as the Director of the Center for Virtual Colonoscopy at Boston Medical Center and is currently Medical Director of the Boston Diagnostics Center for Virtual Colonoscopy.

Dr. Chaoui has published numerous articles and studies, as well as lectured across the USA and internationally, on Virtual Colonoscopy and other areas of radiology.

Internal

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Princeton Longevity Center :: Staff Bios

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life span | Britannica.com

Thursday, August 4th, 2016

Alternative title: longevity

Life span, mayflyG.E. HydeNHPA/EB Inc.the period of time between the birth and death of an organism.

longevity: animalsEncyclopdia Britannica, Inc.It is a commonplace that all organisms die. Some die after only a brief existence, like that of the mayfly, whose adult life burns out in a day, and others like that of the gnarled bristlecone pines, which have lived thousands of years. The limits of the life span of each species appear to be determined ultimately by heredity. Locked within the code of the genetic material are instructions that specify the age beyond which a species cannot live given even the most favourable conditions. And many environmental factors act to diminish that upper age limit.

The maximum life span is a theoretical number whose exact value cannot be determined from existing knowledge about an organism; it is often given as a rough estimate based on the longest lived organism of its species known to date. A more meaningful measure is the average life span; this is a statistical concept that is derived by the analysis of mortality data for populations of each species. A related term is the expectation of life, a hypothetical number computed for humans from mortality tables drawn up by insurance companies. Life expectancy represents the average number of years that a group of persons, all born at the same time, might be expected to live, and it is based on the changing death rate over many past years.

The concept of life span implies that there is an individual whose existence has a definite beginning and end. What constitutes the individual in most cases presents no problem: among organisms that reproduce sexually the individual is a certain amount of living substance capable of maintaining itself alive and endowed with hereditary features that are in some measure unique. In some organisms, however, extensive and apparently indefinite growth takes place and reproduction may occur by division of a single parent organism, as in many protists, including bacteria, algae, and protozoans. If these divisions are incomplete, a colony results; if the parts separate, genetically identical organisms are formed. In order to consider life span in such organisms, the individual must be defined arbitrarily since the organisms are continually dividing. In a strict sense, the life spans in such instances are not comparable to those forms that are sexually produced.

The beginning of an organism can be defined by the formation of the fertilized egg in sexual forms; or by the physical separation of the new organism in asexual forms (many invertebrate animals and many plants). In animals generally, birth is considered to be the beginning of the life span. The timing of birth, however, is so different in various animals that it is only a poor criterion. In many marine invertebrates the hatchling larva consists of relatively few cells, not nearly so far along toward adulthood as a newborn mammal. For even among mammals, variations are considerable. A kangaroo at birth is about an inch long and must develop further in the pouch, hardly comparable to a newborn deer, who within minutes is walking about. If life spans of different kinds of organisms are to be compared, it is essential that these variations be accounted for. The end of an organisms existence results when irreversible changes have occurred to such an extent that the individual no longer actively retains its organization. There is thus a brief period during which it is impossible to say whether the organism is still alive, but this time is so short relative to the total length of life that it creates no great problem in determining life span.

Some organisms seem to be potentially immortal. Unless an accident puts an end to life, they appear to be fully capable of surviving indefinitely. This faculty has been attributed to certain fishes and reptiles, which appear to be capable of unlimited growth. Without examining the various causes of death in detail (see death) a distinction can be made between death as a result of internal changes (i.e., aging) and death as a result of some purely external factor, such as an accident. It is notable that the absence of aging processes is correlated with the absence of individuality. In other words, organisms in which the individual is difficult to define, as in colonial forms, appear not to age.

Plants grow old as surely as do animals. However, a generally accepted definition of age in plants has not yet been realized. If the age of an individual plant is that time interval between the reproductive process that gave rise to the individual and the death of the individual, the age attained may be given readily for some kinds of plants but not for others. The Table lists maximum ages, both estimated and verified, for some seed plants.

Maximum ages for some seed plants

An English oak that has 1,000 annual rings in the trunk is 1,000 years old. But age is less certain in the case of an arctic lupine that germinated from a seed that, containing the embryo, had been lying in a lemmings burrow in the arctic permafrost for 10,000 years.

The mushroom caps that appear overnight last for only a few days, but the network of fungus filaments in the soil (the mycelia) may be as old as 400 years. Because of important differences in structure, the life span of higher plants cannot be compared with that of higher animals. Normally, embryonic cells (that is, cells capable of changing in form or becoming specialized) cease to exist very early in the life of an animal. In plants, however, embryonic tissuethe plant meristemsmay contribute to growth and tissue formation for a much longer time, in some cases throughout the life of the plant. Thus the oldest known trees, bristlecone pines of California and Nevada, have one meristem (the cambium) that has been adding cells to the diameter of these trees for, in many cases, more than 4,000 years and another meristem (the apical) that has been adding cells to the length of these trees for the same period. These meristematic tissues are as old as the plant itself; they were formed in the embryo. The wood, bark, leaves and cones, however, live for only a few years. The wood of the trunk and roots, although dead, remains a part of the tree indefinitely, but the bark, leaves, and cones are continually in the process of dying and sloughing off.

Among the lower plants only a few mosses possess structures that enable an estimate of their age to be made. The haircap moss (Polytrichum) grows through its own stem tip each year, leaving a ring of scales that marks the annual growth. Three to five years growth in this moss is common, but life spans of 10 years have been recorded. The lower portions of such a moss are dead, though intact. Peat moss (Sphagnum) forms extensive growths that fill acid bogs with a peaty turf consisting of the dead lower portions of mosses whose living tops continue growing. Mosses that become encrusted with lime (calcium carbonate) and form tufa beds several metres thick also have living tips and dead lower portions. On the basis of their observed annual growth, some tufa mosses are estimated to have been growing for as long as 2,800 years.

No reliable method for determining the age of ferns exists, but on the basis of size attained and growth rate, some tree ferns are thought to be several decades old. Some club mosses, or lycopsids, have a storied growth pattern similar to that of the haircap moss. Under favourable conditions some specimens live five to seven years.

The woody seed plants, such as conifers and broadleaf trees, are the most amenable to determination of age. In temperate regions, where each years growth is brought to an end by cold or dryness, every growth period is limited by an annual ringa new layer of wood added to the diameter of the tree. These rings may be counted on the cut ends of a tree that has been felled or, using a special instrument, a cylinder of wood can be cut out and the growth rings counted and studied. In the far north growth rings are so close together that they are difficult to count. In the moist tropics growth is more or less continuous, so that clearly defined rings are difficult to find.

Often the age of a tree is estimated on the basis of its diameter, especially when the average annual increase in diameter is known. The source of greatest error in this method is the not infrequent fusing of the trunks of more than one tree, as, for example, occurred in a Montezuma cypress in Santa Mara del Tule, a little Mexican village near Oaxaca. This tree, described by the Spanish explorer Hernan Corts in the early 1500s, was earlier estimated on the basis of its great thickness to be 6,000 years old; later studies, however, proved it to be three trees grown together. Estimates of the age of some English yews have been as high as 3,000 years, but these figures, too, have turned out to be based on the fusion of close-growing trunks, none of which is more than 250 years old. Increment borings of bristlecone pines have shown specimens in the western United States to be 4,600 years old.

Plants, usually herbaceous, that live for only one growing season and produce flowers and seeds in that time are called annuals. They may be represented by such plants as corn and marigolds, which spend a period of a few weeks to a few months rapidly accumulating food materials. As a result of hormonal changesbrought about in many plants by changes in environmental factors such as day length and temperatureleaf-producing tissues change abruptly to flower-producing ones. The formation of flowers, fruits, and seeds rapidly depletes food reserves and the vegetative portion of the plant usually dies. Although the exhaustion of food reserves often accompanies death of the plant, it is not necessarily the cause of death.

These plants, too, are usually herbaceous. They live for two growing seasons. During the first season, food is accumulated, usually in a thickened root (beets, carrots); flowering occurs in the second season. As in annuals, flowering exhausts the food reserves, and the plants die after the seeds mature.

These plants have a life span of several to many years. Some are herbaceous (iris, delphinium), others are shrubs or trees. The perennials differ from the above-mentioned groups in that the storage structures are either permanent or are renewed each year. Perennials require from one to many years growth before flowering. The preflowering (juvenile) period is usually shorter in trees and shrubs with shorter life spans than in those with longer life spans. The long-lived beech tree (Fagus sylvatica), for example, passes 3040 years in the juvenile stage, during which time there is rapid growth but no flowering.

Some plantscotton and tomatoes, for exampleare perennials in their native tropical regions but are capable of blooming and producing fruits, seeds, or other useful parts in their first year. Such plants are often grown as annuals in the temperate zones.

Although there is great variety in the longevity of seeds, the dormant embryo plant contained within the seed will lose its viability (ability to grow) if germination fails to occur within a certain time. Reports of the sprouting of wheat taken from Egyptian tombs are unfounded, but some seeds do retain their viability a long time. Indian lotus seeds (actually fruits) have the longest known retention of viability. On the other hand, seeds of some willows lose their ability to germinate within a week after they have reached maturity.

The loss of viability of seeds in storage, although hastened or retarded by environmental factors, is the result of changes that take place within the seed itself. The changes that have been investigated are: exhaustion of food supply; gradual denaturing or loss of vital structure by protoplasmic proteins; breakdown of enzymes; accumulation of toxins resulting from the metabolism of the seed. Some self-produced toxins may cause mutations that hamper seed germination. Since seeds of different species vary greatly in structure, physiology, and life history, no single set of age factors can apply to all seeds.

Much of what is known of the length of life of animals other than man derives from observations of domesticated species in laboratories and zoos. One has only to consider how few animals reveal their age to appreciate the difficulties involved in answering the apparently simple question of how long they live in nature. In many fishes, a few kinds of clams, and an occasional species of other groups, growth is seasonal, so that annual zones of growth, much like tree rings, are produced in some part of the organism. Among game species, methods of determining relative age by indicators such as the amount of tooth wear or changes in bone structure have yielded valuable information. Bird bands and other identifying marks also make age estimation possible. But one of the consequences of the fact that animals move is that very little is known about the life span of most species as they exist in nature.

The extreme claims of longevity that are occasionally made for one species or another have consistently been proven false when subjected to critical scrutiny. Although the maximum life span that has been observed for a particular species cannot be considered absolute, since a limited number of individuals at best has been studied, this datum probably provides a fair approximation of the greatest age attainable for this kind of animal under favourable conditions. Animals in captivity, which provide most of the records of extreme age, are exposed to far fewer hazards than those in the wild. In the accompanying table of maximum longevity, particular species have been so selected as to encompass the known range of longevity of other members of the taxonomic group to which they belong.

Maximum longevity of animals in captivity

Life span usually is measured in units of time. Although this may seem eminently logical, certain difficulties may arise. In cold-blooded animals in general, the rate of metabolism that determines the various life processes varies with the temperatures to which they are exposed. If aging depends on the expenditure of a fixed amount of vital energy, an idea first proposed in 1908, life span will vary tremendously depending on temperature or other external variables that influence life span. There is considerable evidence attesting at least to the partial cogency of this argument. So long as a certain range is not exceeded, cold-blooded invertebrates do live longer at low than at high temperatures. Rats in the laboratory live longest on a somewhat restricted diet that does not permit maximum metabolic rate. Of perhaps even greater significance is the fact that many animals undergo dormant periods. Many small mammals hibernate; a number of arthropods have life cycles that include periods during which development is arrested. Under both conditions the metabolic rate becomes very low. It is questionable whether such periods should be included in computing the life span of a particular organism. Comparisons between species, some of which have such inactive periods while others do not, are dangerous. It is possible that life span could be measured more adequately by total metabolism; however, the data that are necessary for this purpose are almost entirely lacking.

Length of life is controlled by a multitude of factors, which collectively may be termed environment, operating on a genetic system that determines how the individual will respond. It is impossible to list all the environmental factors that may lead to death. For analytical purposes it is, however, useful to make certain formal separations. Every animal is exposed to (1) a pattern of numerous events, each with a certain probability of killing the individual at any moment and, in the aggregate, causing a total probability of death or survival; (2) climatic and other changes in the habitat, modifying the frequency with which the various potentially fatal events occur; and (3) progressive systemic change, inasmuch as growth, reproduction, development, and senescence are characteristics intrinsic in the organism and capable of modifying the effects of various environmental factors.

Consider a group of similar animals of the same age. Although no two individuals can have precisely the same environment, let it be assumed that the environment of the group remains effectively constant. If the animals undergo no progressive physiological changes, the factors causing death will produce a death rate that will remain constant in time. Under these conditions, it will take the same amount of time for the population to become reduced to one-half its former number, no matter how many animals remain at the beginning of the period considered. The animals therefore survive according to the pattern of an accident curve. This is the sense in which many of the lower animals are immortal. Although they die, they do not age; how long they have already lived has no influence on their further life expectation.

Another group of animals may consist of individuals that differ markedly in their responses to the constant environment. They may be genetically different, or their previous development may have caused variations to arise. Those individuals that are most poorly suited to the new environment will die, leaving survivors that are better adapted. The same result can also be achieved in other ways. If the environment varies geographically, those individuals that happen to find areas in which existence can be maintained will survive, while the remainder will die. Or, as a result of their own properties, animals in a constant environment may acclimate in a variety of ways, thus adjusting to the existing conditions. The pattern of survival that results in each of these cases is one in which the death rate declines with time, as illustrated by the selectionacclimation curve.

In the absence of death from other causes, all members of a population may exist in their environment until the onset of senescence, which will cause a decline in the ability of individuals to survive. In a sense they can be considered to wear out as does a machine. Their survival is best described by individual differences among members of the population that determine the curvature of the survival line (wearing-out curve). The more the population varies, the less abrupt is the transition from total survival to total death.

Under the actual conditions of existence of animals the three types of survival (accident pattern, selectionacclimation pattern, wearing-out pattern) above all enter as components of the realized survival pattern. Thus in animals that are carefully maintained in the laboratory, survival is approximately that of the wearing-out pattern. Environmental accidents can be kept to a minimum under these conditions, and survival is almost complete during the major part of the life span. In all known cases, however, the early stages of the life span are characterized by a noticeable contribution of the selectionacclimation pattern. This must be interpreted as a result of developmental changes that accompany the early life of the individuals and of selective processes that operate on those organisms whose genetic constitutions are ill fitted for that environment.

In some of the larger mammals in nature, the existing evidence points to a similar survival pattern. In a variety of other animals, however, and including fishes and invertebrates, mortality in the young stages is so high that the selectionacclimation curve predominates. One estimate places the mortality of the Atlantic mackerel during its first 90 days of life as high as 99.9996 percent. Since some mackerel do live for several years, a mortality rate that decreases with age is indicated. Similar considerations probably apply to all those animals that have larval stages that serve as dispersal mechanisms.

When the postjuvenile portion of the life span is considered by itself, a number of animals for which such information has been gatheredincluding primarily fishes and birdshave survivorship curves that are dominated by the accident pattern. In these species in nature, death from old age apparently is rare. Their chance of surviving to an advanced age is so small that it may be statistically negligible. In modern times, human predation is a large factor in the mortality of these species in many cases. Since deaths from fishing and hunting are largely independent of age, once an animal has reached a certain minimum size, such a factor only makes the survival curve steeper but does not change its shape. One consequence of such increased mortality is that fewer old and large individuals are noticed in a population.

More complex survival patterns, such as the hypothetical one illustrated, undoubtedly exist. They should be looked for in those species in which extensive reorganization of the animal is part of the normal life cycle. In effect, these animals change their environment radically, in some cases several times during a lifetime. The frog offers a familiar example. During its period of early development and until shortly after hatching, the animal is subject to major internal, and some external, change. As a tadpole it is adjusted to an aquatic, herbivorous life. The metamorphosis to the terrestrial, carnivorous adult form is accompanied by varied physiological stresses that must be expected to produce a temporary increase in mortality rate. In some insects the eggs, larvae, pupae, and adults are exposed to and respond to quite different environments, and a survivorship pattern even more complex than that described by the composite curve may exist.

The same species will exhibit changed survival in different environments. In captivity an animal population may approach the wearing-out pattern; in its natural habitat survivorship may vary with age in a quite different way. Although one can assign a maximum potential life span to an individualwhile realizing that this maximum may not be attainedit is impossible to specify the survivorship pattern unless the environment is also specified. This is another way of saying that life span is the joint property of the animal and the environment in which it lives.

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New England Centenarian Study BUMC

Thursday, August 4th, 2016

New England Centenarian Study

To Discover the Secrets of A Long Healthy and Happy Life

Our two major studies are the New England Centenarian Study (founded 1995) and the multi-center Long Life Family Study (Boston Medical Center is one of 5 study sites),established in 2006.

We are actively seekingparticipants to be in the New England Centenarian Study. The criteria are simply subjects age 103+ years oldor 100+ years with siblings.

If you would like to contact the study, please call us at 888-333-6327 (toll free) where you will hear a menu tobe connected toa member of the research staff (please choose this option). You can alsoemail the study manager, Stacy Andersen PhD at stacy@bu.edu or the Principal Investigator, Thomas Perls MD, MPH at thperls@bu.edu.

The New England Centenarian Study is funded by:

The Martin A. Samowitz Foundation

Since 2006, the Long Life Family Studyhas beenconducting a prospective study of 5,000 subjects belonging to about 550 families that demonstrateparticularly unusualclustering for exceptional longevity. The Long Life Family Study is funded by and collaborates closely with The National Institute on Aging.

Pleasecall Dr. Thomas Perls toll-free at 888-333-6327 or email him at thperls@bu.edu if you or a family member wish to discuss our studies, find out more information regarding enrollment or to discuss supporting our studies.

MEDIA INQUIRES: Please contact

Jenny Eriksen Leary Manager of Media Relations Boston Medical Center 617-638-6841 jenny.eriksen@bmc.org

Genes play a critical and complex role in facilitating exceptional longevity. The genetic influence becomes greater and greater with older and older ages, especially beyond 103 years of age.

Citation: Genetic Signatures of Exceptional Longevity in Humans. Paola Sebastiani, Nadia Solovieff, Andrew T. DeWan, Kyle M. Walsh, Annibale Puca, Stephen W. Hartley, Efthymia Melista, Stacy Andersen, Daniel A. Dworkis, Jemma B. Wilk, Richard H. Myers, Martin H. Steinberg, Monty Montano, Clinton T. Baldwin, Josephine Hoh, Thomas T. Perls. PloS ONE 2012. DOI: 10.1371/journal.pone.0029848.

Many of the above genetic findings were replicated in a combination of 5 collaborating centenarian studies.

Citation: Meta-analysis of genetic variants associated with human exceptional longevity. Paola Sebastiani, Harold Bae1, Fangui X. Sun, Stacy L. Andersen, E. Warwick Daw, Alberto Malovini, Toshio Kojima, Nobuyoshi Hirose, Nicole Schupf, Annibale Puca, Thomas T Perls. Aging (Albany NY) 2013 September; 5(9): 653661. Published online 2013 August 24. PMCID: PMC3808698

In another paper published January, 2012, we have produced perhaps some of our most exciting findings to date. Early oninThe New England Centenarian Study, we thought that centenarians had to markedly delay or even escape age-related diseases like heart attacks, stroke, diabetes and Alzheimers, or else they would never be able to get to their very old ages. In fact, in 1980, a Stanford researcher named James Fries proposed the Compression of Morbidity hypothesis which states that as one approaches the limit of human life span, they must compress the time that they develop diseases towards the very end of their life and he proposed that people around the age of 100 do this. However, in 2003 we found that many of our centenarian subjects had age related diseases even before the age of 80 (about 43%, and whom we called survivors), after the age of 80 (about 42% and whom we called delayers) and lastly, those who had no mortality-associated diseases at age 100 (about 15% and whom we called escapers). The key though was that 90% of all of the centenarians were still independently functioning at the average age of 93 years. Somehow, despite the presence of diseases, people who become centenarians dont die from those diseases, but rather they are able to deal with them much better than other people and remain independently functioning more than 30 years beyond the age of 60. Therefore it seemed to us that for these study participants, it was not so much the compression of morbidity that was important to their survival, but rather a compression of disability.

In this current paper though, titled Health span approximates life span among many supercentenarians: Compression of morbidity at the approximate limit of life span, we have found that we just werent looking at old enough subjects when investigating Jim Fries hypothesis. As some of you know, over the past few years we have been working hard on recruiting and enrolling the most extreme old, supercentenarians who are people that live to 110 years and older. Once we enrolled our hundredth super-centenarian (by far the largest collection of supers in the world), we were able to investigate whether or not people who truly approach the limit of human lifespan actually compress their morbidity towards the end of their lives. Inour study of a reference group, nonagenarians (subjects in their nineties), centenarians (ages 100-104), semi-supercentenarians (ages 105-109) and supercentenarians(ages 110+), the subjects had progressively shorter periods of their lives spent with age-related diseases, from 17.9% of their lives in the referent group, to 9.4% in the nonagenarians and down to 5.2% in the supercentenarians. These findings support the compression of morbidity hypothesis and the idea that there truly is a limit to human life span 125 years. Also the supercentenarians were much more alike in terms of the markedly delayed age of onset of age-related diseases compared to the subjects age 100-104 who were quite heterogeneous. That homogeneity indicates they must have some factors (presumably genetic) in common that allow them to be so similar. We believe that our oldest subjects, ages 105+ years, give us the best chance and discovering these genes.

Citations: Health span approximates life span among many supercentenarians: Compression of morbidity at the approximate limit of life span Andersen SL, Sebastiani P, Dworkis DA, Feldman L, Perls T. J Gerontol A Biol Sci Med Sci 2012;67A:395-405.

Families Enriched for Exceptional Longevity also have Increased Health-Span: Findings from the Long Life Family Study. Paola Sebastiani, Fangui X. Sun, Stacy L. Andersen, Joseph H. Lee, Mary K. Wojczynski, Jason L. Sanders, Anatoli Yashin, Anne B. Newman, Thomas T. Perls. Front Public Health. 2013; 1: 38. Prepublished online 2013 August 16. Published online 2013 September 30. doi:10.3389/fpubh.2013.00038. PMCID: PMC3859985.

The New England Centenarian Study, along with collaborators at the Scripps Institute and the University of Florida, Gainesville, performed and published the first-ever whole genome sequence of a supercentenarian and actually not one super, but two, both over the age of 114 years and one was a man and the other a woman. As with our paper on the genetic signatures of exceptional longevity, we found here as well that centenarians have just as many genetic variants associated with diseases as the general population. However, they likely also have longevity-associated variants that counteract such disease genes, thus allowing for slower aging and increased resistance to age-related diseases.

In this paper we also found several genes that occurred in our published genetic prediction model which had coding regions that led to differences in gene function. These findings support the validity of the genetic prediction model. The New England Centenarian Study has posted the whole genome sequences of these two subjects on a data repository (called dbGaP) based at the National Institutes of Health. This will allow researchers from around the world to access all of the data and use them for their own research. Our hope is that these data will lead to important discoveries about genes that help delay or allow the escape from age related diseases like Alzheimers disease.

Citation: Whole genome sequences of male and female supercentenairnas, Both ages >114 years. Sebastiani P, Riva A, Montano M, Pham P, Torkamani A, Scherba E, Benson G, Milton JN, Baldwin CT, Andersen S, Schork NJ, Steinberg MH, Perls T. Frontiers in Genetics of Aging 2012;2.

There is a growing body of evidence for a substantial genetic influence upon survival to the most extreme ages. An important question is what would be the selection pressure(s) for the evolution of longevity associated genetic variants. The pressure to have a longer period of time during which women can bear children and therefore have more of them and therefore have greater success in passing ones genes down to subsequent generations could be one such pressure. This hypothesis is consistent with the disposable soma theory where the tradeoff in energy allocation between reproductive fitness and repair/maintenance functions can be delayed when longevity associated variants facilitate slower aging and the delay or prevention of age-related diseases that also adversely affect fertility. Several studies have noted an association between older maternal age and an increased odds of exceptional survival. The New England Centenarian Study assessed maternal age history in its sample of female centenarians and a birth-cohort-matched referent sample of women who survived to the cohorts average life expectancy. Women who gave birth to a child after the age of 40 (fertility assistance was not technologically available to this cohort) had a four times greater odds of being a centenarian. Numerous investigators are now searching for and investigating genes that influence reproductive fitness in terms of their ability to also influence rate of aging and susceptibility to age-related diseases.

Citations: Middle-aged mothers live longer.Perls TT, Alpert L, Fretts RC. Nature. 1997 Sep 11;389(6647):133.PMID: 9296486 [PubMed indexed for MEDLINE]

Extended maternal age at birth of last child and womens longevity in the Long Life Family Study.Sun F, Sebastiani P, Schupf N, Bae H, Andersen SL, McIntosh A, Abel H, Elo IT, Perls TT. Menopause. 2015 Jan;22(1):26-31. doi: 10.1097/GME.0000000000000276. PMID: 24977462. [PubMed in process]

The reappearance of procaine hydrochloride (Gerovital H3) for antiaging.Perls T. J Am Geriatr Soc. 2013 Jun;61(6):1024-5. doi: 10.1111/jgs.12278. No abstract available. PMID: 23772727. [PubMed indexed for MEDLINE]

Growth hormone and anabolic steroids: athletes are the tip of the iceberg.Perls TT. Drug Test Anal. 2009 Sep;1(9-10):419-25. doi: 10.1002/dta.87. PMID: 20355224 [PubMed indexed for MEDLINE]. Abstract: Professional Athletes misuse of anabolic steroids, growth hormone and other drugs are the tip of a very large, mostly ignored iceberg, made up of people who receive these drugs for such non-medical uses as body-building, school sports and anti-aging. Although these drugs are often used in combination, this article focuses on growth hormone. Fuelling the demand for these drugs are drug manufacturers, pharmacies, websites, clinics and their doctors.

New developments in the illegal provision of growth hormone for anti-aging and bodybuilding.Olshansky SJ, Perls TT. JAMA. 2008 Jun 18;299(23):2792-4. doi: 10.1001/jama.299.23.2792. No abstract available. PMID: 18560007 [PubMed indexed for MEDLINE]

DHEA and testosterone in the elderly.Perls TT. N Engl J Med. 2007 Feb 8;356(6):636; author reply 637. No abstract available. PMID: 17288051 [PubMed indexed for MEDLINE]

Hope drives antiaging hype.Perls TT. Cleve Clin J Med. 2006 Dec;73(12):1039-40, 1044. Review. No abstract available. PMID: 17190307 [PubMed indexed for MEDLINE]

Provision or distribution of growth hormone for antiaging: clinical and legal issues.Perls TT, Reisman NR, Olshansky SJ. JAMA. 2005 Oct 26;294(16):2086-90. No abstract available. PMID: 16249424 [PubMed indexed for MEDLINE]

Anti-aging quackery: human growth hormone and tricks of the trademore dangerous than ever.Perls TT. J Gerontol A Biol Sci Med Sci. 2004 Jul;59(7):682-91. PMID: 15304532 [PubMed indexed for MEDLINE]

The hype and the realitypart I.Olshansky SJ, Hayflick L, Perls TT. J Gerontol A Biol Sci Med Sci. 2004 Jun;59(6):B513-4. No abstract available. PMID: 15215255 [PubMed indexed for MEDLINE]

Antiaging medicine: what should we tell our patients? Perls T. Aging HealthApril 2010, Vol. 6, No. 2, Pages 149-154 , DOI 10.2217/ahe.10.11 (doi:10.2217/ahe.10.11)

To speak to someone about our research, please call our toll free number: 1-888-333-NECS (6327). Choose the option to speak with a member of our staff and you will be directed to the right person.

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New England Centenarian Study BUMC

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The benefits of mucuna pruriens are … – Secrets of Longevity

Thursday, August 4th, 2016

The amazing herbal adaptogen that is mucuna pruriens is well known for it's wide range of tonifying, strengthening and all around beneficial properties. Perhaps it is best known as a potent herbal aphrodisiac. This Indian herb is known by many names, some of which are cowitch, cowhage, velvet beans, sea beans, buffalo beans, Kapikachu, Atmagupta and many more!

The prickly orange hairs on the outside of the pod cause severe itching when they come in contact with the skin. The doctrine of signatures can give us a clue here since the velvet bean's pods can be used to treat snake bite! The main medicinal effects attributed to mucuna pruriens come from the seeds, but the pod and its hairs and the plant's roots can also be used in herbal preparations. The velvet beans are "drift seeds", which is a name given to any seeds that can float away on ocean currents to grow in other regions of the world.

~Sweet, bitter and hot

~Heavy and unctuous (oily or greasing quality)

~Balancing to all three doshas! (a rare quality even amongst herbal adaptogens, ginseng and gotu kola are also known for this)

~Builds fertility in men (Increases semen volume, sperm count and sperm motility, better double up boys...)

~Very potent at increasing libido for both men and women

~Treats leucorrhoea (vaginal discharge), menorrhagia (excessive menstrual bleeding) and spermatorrhoea (involuntary ejaculation) which are all signs of leakage of Jing/Ojas, which is the foundational essence of health

~Helps men last longer sexually

~Used to build muscle in those who are weak

~Helps women increase lactation when breastfeeding

~Prevents and or lowers the effects of poisonous snake bites

~Treats Parkinson's disease

~Treats depression

~Treats insomnia and generally deepens sleep

~The hairs on the mucuna pod are used to treat several species of parasitic worms (excluding tapeworms)

~Helps digestion without increasing pitta (fire)

This link will take you to my favorite mucuna extract to use in smoothies and elixirs. Herbal extracts are easy to use and are extremely bio-available (absorbable) by the body.

If you prefer to work with whole herbs, you can get another amazing brand of Organic Mucuna Seed Powder by clicking this text link.

Mucuna pruriens contains 40mg/g of a compound called L-DOPA which is a direct precursor to the neurotransmitter dopamine. Dopamine works as one of the best natural hgh releasers (human growth hormone) by stimulating the pituitary gland to increase it's production. High levels throughout life of the body's own natural growth hormone (not hormones from the synthetic injections) is known as a major key for human longevity.

Dopamine also increases other youth hormones such as testosterone (it must be mentioned that these increases are never throwing the endocrine system out of balance, merely improving levels which tend to decrease over time in the average person). These resulting increased levels of these hormones from the use of mucuna pruriens extracts, powders and/or raw herbs explains its association with increasing libido, fertility, lean muscle mass, reducing signs of aging such as wrinkles and body fat, increasing bone density and even boosting overall energy levels.

Animal studies have shown powerful results such as a ten fold increase in mounting frequency by male rats! Also a decrease in post ejaculatory intervals have been observed, meaning that the animals being studied are more quickly able to return to "the task at hand". This could be due to the fact that mucuna pruriens extract basically cures premature ejaculation and the amount of downtown between ejaculations by reducing hypersensitivity in the genitals.

L-DOPA from mucuna pruriens has been shown to be safer and more effective for controlling Parkinson's disease than the pharmaceutical drugs Levodopa and Carbidopa. This is because the vast array of other chemical constituents that accompany L-DOPA in the unprocessed plant also play a role in its ability to manage Parkinson's disease. Since Parkinson's is in large part a deficiency of the neurotransmitter dopamine, this adaptogenic herb is crucial for anyone looking to manage this disease. It also looks to be very promising as a treatment for recovering drug addicts and people suffering from depression related illness, since these people have deficiencies of the neurotransmitters serotonin and dopamine (which the velvet beans contain and help balance in the human body).

The anti-snake venom effect of mucuna pruriens extract makes it a great tonic herb for outdoor enthusiasts to take daily. A variety of toxins from snake venom have been found to be reduced or prevented by the supplementation of this herb. Of course, one has to be taking it for it to work and it's best taken all the time since snake bites are completely unpredictable, yet obviously a risk for anyone poking around in the woods and other environments where these creatures hang out.

Enhanced lucid dreaming effects have been reported with the use of this amazing herb. Other chemicals in addition to L-DOPA found in mucuna pruriens that can have a mind altering effect include serotonin (5HT), oxitriptan (5-HTP), nicotine, N,N-DMT, bufotenin (5-HO-DMT) and 5-MeO-DMT. These would explain its noted effects as an entheogenic substance often found in Ayahuasca preparations (an Amazonian psychedelic shamanic herbal preparation). Do not be alarmed however, these chemicals are not in present in high enough quantities to cause "reality altering" effects, unless the herb happens to be combined with a sufficient amount of an MAOI 😉

This herbal adaptogen can also be used by anyone simply wanting to have fun. The abundance of bliss chemicals combined with the velvet beans adept ability at helping men last longer sexually and increasing libido for both genders makes this a safe and hilariously fun herb to use recreationally. It is also quickly becoming popular as a natural bodybuilding hgh secretagogue. This is much safer to use than synthetic human growth hormone which is quickly gaining a reputation as a carcinogenic "steroid-like" performance enhancer. The great thing with this herb is that it gets your body to make growth hormone itself and thus control the amount it makes and avoid the problems associated with elevated levels of hgh.

This link will take you to my favorite mucuna extract to use in smoothies and elixirs. Herbal extracts are easy to use and are extremely bio-available (absorbable) by the body.

If you prefer to work with whole herbs, you can get another amazing brand of Organic Mucuna Seed Powder by clicking this text link.

One of the most important secrets of longevity is maintaining optimal levels of key hormones as well as other phytochemical factors in your bloodstream. This article has already covered how mucuna pruriens is a natural growth hormone secretagogue (hgh) as well as a booster of other hormones of youth that tend to diminish with time. It has been found that blood plasma levels of some of the top antioxidants such as superoxide dismutase (SOD), catalase (an enzyme that prevents your hair from going gray!), glutathione (GSH) and ascorbic acid (vitamin C) are kept elevated in those who take this adaptogenic herbal aphrodisiac.

The powerful benefits of mucuna pruriens extract and whole herb should be temporarily avoided while pregnant or suffering from diabetes (it has blood sugar lowering properties). It should also be avoided by anyone with schizophrenia. If you choose to use adaptogenic herbs to manage or reverse any disease or disorder, always work with a knowledgeable health care practitioner. There is no specifically determined dosage for this herbal aphrodisiac, however most people agree on 15-30 grams a day for adults as a safe and effective amount.

Sources:

~http://ecam.oxfordjournals.org/cgi/content/abstract/nem171 ~http://herbal-powers.com/macunapruriens1.html ~http://www.herbalcureindia.com/herbs/mucuna-pruriens.htm ~http://en.wikipedia.org/wiki/Mucuna_pruriens ~http://www.ncbi.nlm.nih.gov/pubmed/18203263?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=19 ~http://www.ncbi.nlm.nih.gov/pubmed/18973898?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=15

Click to return from "Mucuna Pruriens" to the "Adaptogenic Herbs" page.

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The benefits of mucuna pruriens are ... - Secrets of Longevity

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At 100, The Secret of David Rockefellers Longevity …

Thursday, August 4th, 2016

Organ transplants.

Cannibalizing the dead.

Fitting for one of the worlds chiefSatanists, responsible forthe

deaths of millions.

Last week (June 12), David Rockefeller celebrated his 100th birthday without much ado.

He said the secret of his longevity was leading a simple life.

People often ask me this question and I always answer the same thing: Love life. Live a simple life, play with your kids, enjoy the things you have, spend time with good loyal friends.

He might have added that having a heart transplant every 6-7 years might have been a factor.

Rockefeller has had six heart transplants since 1976 when a car accident led him to suffer aheart attack. He has also had two kidney transplants in 1988 and 2004.

Just two months ago, the billionaire philanthropist had his sixth heart transplant.

The heart transplant surgery, which lasted 6 hours and was done by a team of private surgeons at his principal residence, on the family estate in Pocantico Hills, New York, doesnt seem to have tired the legendary business man known for his dynamism and cunningness.

With all the carnage due to the Illuminati agenda, there are plenty of beating hearts for him to pillage.

Note:

Memoirs (2003)[edit]

ISBN-13: 978-0812969733

For more than a century, ideological extremists at either end of the political spectrum have seized upon well-publicized incidents such as my encounter with Castro to attack the Rockefeller family for the inordinate influence they claim we wield over American political and economic institutions. Some even believe we are part of a secret cabal working against the best interests of the United States, characterizing my family and me as internationalists and of conspiring with others around the world to build a more integrated global political and economic structure one world, if you will. If that is the charge, I stand guilty, and I am proud of it.

The anti-Rockefeller focus of these otherwise incompatible political positions owes much to Populism. Populists believe in conspiracies and one of the most enduring is that a secret group of international bankers and capitalists, and their minions, control the worlds economy. Because of my name and prominence as head of the Chase for many years, I have earned the distinction of conspirator in chief from some of these people.

Populists and isolationists ignore the tangible benefits that have resulted in our active international role during the past half-century. Not only was the very real threat posed by Soviet Communism overcome, but there have been fundamental improvements in societies around the world, particularly in the United States, as a result of global trade, improved communications, and the heightened interaction of people from different cultures. Populists rarely mention these positive consequences, nor can they cogently explain how they would have sustained American economic growth and expansion of our political power without them.

Ch. 27 : Proud Internationalist, p. 406

https://en.wikiquote.org/wiki/David_Rockefeller

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At 100, The Secret of David Rockefellers Longevity ...

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How Long Will I Live? – Life Expectancy Calculator

Friday, October 23rd, 2015

We have been working to update the interface of the tool and integrate the latest available data into our calculations. Shortly, this version of the calculator will be replaced. The beta version of the updated calculator is available here. Feedback? Fill out this quick survey to let us know. Fill in the following form then click the button labeled "Calculate Life Expectancy". For values which you are unsure of, leave it blank or choose option 'don't know'; For zero values, enter "0", DO NOT leave them blank If you're in a hurry, try our Short life expectancy calculator.

I am year old male female white nonwhite My height is inches (NOTE!!! Only input inches: Eg. 5'8" = 68 inches) My weight is pounds I expect to have less than 10 10 to 11 more than 11 don't know years of education My family's total income for the past 12 months is dollars I expect that for most of my life I will be married not married don't know Compared to other people of the same age and sex as me, I am in the 1st (least fit) 2nd 3rd 4th 5th (fittest) don't know quintile of fitness(refer to Fitness Table) I do not do don't know have at least one first degree relative (parents, sibling, children) who has a history of heart diseases I do not do don't know have at least one first degree relative (parents, sibling, children) who has a history of prostate cancer I do not do don't know have at least one first degree relative (parents, sibling, children) who has a history of breast cancer I do not do don't know have at least one first degree relative (parents, sibling, children) who has a history of colorectal cancer I do not do don't know have at least one first degree relative (parents, sibling, children) who has a history of stomach cancer I do not do don't know have at least one first degree relative (parents, sibling, children) who has a history of lung cancer None One Two or more don't know of my first degree relative (parents, sibling, children) has a history of diabetes I do not do don't know have at least one first degree relative (parents, sibling, children) who has a history of stroke I reside in Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware District of Columbia Florida Georgia Hawaii Idaho Illnois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming don't know I have not have don't know been diagnosed with asthma I have not have don't know been diagnosed with diabetes My diastolic blood pressure (the smaller/bottom number- an average adult's is about 80) is mmHg

I smoke cigarettes per day My spouse smokes cigarettes per day I have 0 or negligible less than 1 1 2 to 3 4 or more don't know drinks per day I travel thousand miles per year in an automobile The driver of the automobile which I most frequently travel in is a male female don't know The age of the driver of the automobile which I most frequently travel in is years I do not do don't know regularly wear seat belts when travelling in a automobile The automobile which I most frequently travel in does not does don't know regularly keep to speeds appropriate to road conditions The driver of the automobile which I most frequently travel in is sometimes never don't know drunk while driving Of the 10 things listed in the Stress List, of them happened to me in the past 12 months I am a sedentary person occasional exerciser conditioning exerciser don't know I work in the mining construction transportation/public utilities agriculture/forestry/fishing public administration manufacturing retail trade services wholesale trade finance/real estate all others don't know industry My father worked in a non-manual manual don't know job My first regular occupation is a non-manual manual don't know job My current occupation is a non-manual manual don't know job Of the 5 types of food in the Dietary Diversity List, on average I consume types more less don't know than 10% of my energy intake comes from fat I am not am don't know among the 15% most depressed of the population I have had sexual partners in the past 12 months For most of my sexual encounters, I do not do don't know use condoms On average, I have hours of sleep a day

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The Big Physical: Where to Go, What to Get | Departures

Friday, October 9th, 2015

While getting old may beat the alternative, living in denial is a comfortable choiceand a lot more pleasant than your first colonoscopy. The annual checkup at your doctors office covers the basics, but a truly thorough medical exam will involve trips to several offices, with the usual long waits and patients stacked up like planes over Chicagos OHare. Two years ago one of my closest friends died from a coronary that absolutely could have been prevented had he only taken the time from his crazy work schedule and family obligations for a checkup.

With baby boomers starting to age, there has been a proliferation of facilities offering comprehensive "executive" physicals. Having just turned 50 myself, I figured this might be a good time to see how the examsand my bodyhave evolved. Among the best-known options, the Mayo and Cleveland clinics, along with the Johns Hopkins, Duke, UCLA, and Stanford units, are all associated with major hospitalswhich is useful should serious complications be found or immediate treatment be recommended. According to the Mayo Clinic, less than 5 percent of its exams revealed potentially life-threatening conditions and almost half exposed risk factors for serious illness. These centers draw patients from all over the world and focus not just on medical needs but a lifestyle approach as well. The Cleveland Clinic even offers programs through the Canyon Ranch spa resorts. Also available are a number of private diagnostic centers that only perform physical exams, such as the Princeton Longevity Center in New Jersey and Texass Cooper Clinics. I chose the PLC strictly for its convenience, but some might be more comfortable going to a hospital. Others prefer to go the true luxury route and turn their physical into a spa holiday or fit it into a resort vacation. To me, though, the chance of getting some bad medical news before my kelp facial could be a real buzz kill.

As at most centers, the day in the PLC started at the scanning facility, replete with state-of-the-art, 64-slice CT machines. I was then shuttled around the main office, given every sort of workup imaginable, and promised a full report on my mortality within hours. Some centers recommend full-body CT scans for patients over 45. While they can be lifesavers, they are also controversial. Dr. Reginald Munden, interim chair of the department of Diagnostic Radiology at the University of Texas M. D. Anderson Cancer Center, says, "Im not comfortable with a shotgun approach to screening," citing the limited sensitivity of scans to common cancer lesions and the small but significant increase in cancer risk from more radiation exposure. There is also the issue of false positives: Up to 80 percent of such tests may find something that can lead to what Munden calls a spiral of expensive and anxiety-provoking follow-up scans with few meaningful results. Interestingly, just as risky can be false negativesbeing told the scan shows no problems to be concerned about. This can lead some people to continue damaging behavior, such as smoking, or to ignore new symptoms.

Of course, there are many stories of serious problems being caught. Doctors at the clinics have received numerous e-mails from patients whose renal cancer or developing aneurysm was detected early, possibly saving their lives. In fact, the day I was at the PLC an exinvestment banker discovered, after 53 years, that he was born with only one kidney. Balancing the risks against the benefits of a scan is a personal decision, and any clinic should provide you with plenty of information to allow you to make an educated evaluation. Dr. Richard S. Lang, who heads the section of preventive medicine at the Cleveland Clinic, explained that while "the scans may not be for everyone," they certainly "offer additional information to a patients profile" and, so long as the findings are managed properly, can be of great valueeven if just as a baseline for future exams.

After the CTs and blood tests are completed, you can expect a very detailed and unrushed physical from a senior staffer instead of the usual Cliffs Notes version offered by your GP. Every aspect of your medical history will be checkedyou will be asked to send copies of all available reports in advanceand any issues, aches, or pains considered. I then had a challenging cardiovascular stress test and gym session with senior exercise physiologist Chris Volgraf. A highly educated trainer and professional strength coach, he completely changed my perspective on my own workout regimen and showed me a series of warm-ups and exercises designed to make my gym time safer, more efficient, and more effective.

Lunch was followed by a vision and hearing test, a bone density and body composition scan, and a meeting with a nutritionist, who evaluated the three-day food log I had been asked to keep.

When all the tests were done, the biggest difference between a full day at one of the clinics and a quick routine maintenance check became clear: A senior doctor sits down with you and reviews the results of every test in detail and their implications. Seeing rotating, 3-D, full-color computer images of your internal organs can be disquieting. Dr. David Fein, medical director and founder of the PLC, told me that one of the most effective tools in convincing patients to modify their unhealthy lifestyle is showing them their blocked arteries or the vascular fat wrapped around their vital organs in high-definition splendor. "You can point to it and say Thats a picture of your heart attack, or your type 2 diabetes diagnosis in five years. " Pushing the predictive envelope, the Duke Executive Health Program will soon offer a cutting-edge genomic DNAbased assessment that screens for certain genetic risks.

I left the PLC with a hefty binder, complete with test results and a disc containing copies of my scans, to give to my personal physician. In my opinion anyone who can afford it, or whose employer or insurer will pay, should immediately sign up for a visit to one of the top clinics and return at reasonable intervals. The Mayo Clinic quotes studies showing that companies can save as much as 20 percent in additional medical claims and 45 percent in extra sick days taken by executives who have regularly undergone thorough physicals. Its unlikely you have ever gotten so complete and detailed a review of not just the results but also the meaning of routine medical tests, as well as specific and practical advice on diet and exercise. While affiliation with a hospital or a major medical clinic is obviously a plus, the most important thing a diagnostic center can do for you is get you in the door. So if traveling makes you less likely to go, pick a center nearby.

centerforpartnershipmedicine.com Location: Chicago, IL Program:1 day Approx. Cost: $3,000$6,000

clevelandclinic.org; executivehealthprogram.com Location: Cleveland, OH; Weston, FL; Toronto; Canyon Ranch (AZ, MA) Program:13 days Approx. Cost: from $3,000

cooperaerobics.com/clinic Location: Dallas and McKinney, TX Program:1 day Approx. Cost: $1,800$4,000

dukeexechealth.org Location: Durham, NC Program:1 day Approx. Cost: $2,800

execmd.com Location: Menlo Park, CA Program:1/2 day Approx. Cost: $2,000$2,600

hopkinsmedicine.org/gim/clinical/executive_health Location: Baltimore, MD Program:1 day Approx. Cost: $1,800$2,200

mayoclinic.org/executive-health Location: Rochester, MN; Scottsdale, AZ; Jacksonville, FL Program:12 days Approx. Cost: $1,500$6,000

theplc.net Location: Princeton, NJ Program:1 day Approx. Cost: $3,250

exechealth.ucla.edu Location: Los Angeles, CA Program:1 day Approx. Cost: from $2,400

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The Big Physical: Where to Go, What to Get | Departures

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Comprehensive Health Exam :: Princeton Longevity Center

Wednesday, October 7th, 2015

Announcing Our Newest Location in Fairfax, Virginia Call Us for Details!

The Princeton Longevity Comprehensive Exam takes your health beyond the "Annual Physical".

With the latest technology, combined with caring experts who take the time to fully evaluate your health, the Princeton Longevity Center Comprehensive Exam can detect early cancers, heart disease, aneurysms and the "silent killers" that are often missed in a typical physical exam or routine blood tests.

Youll get the latest diagnostic, screening and imaging technologies to assess the state of your health and the detailed information you need to optimize the quality of your future years.

The scope of your examination and the amount of useful information you come away with is dramatically more revealing than a standard physical exam or consultation. The effect on your future can be dramatic.

Our proactive approach to illness and premature aging will help you identify your risk of future disease and create a personalized program to improve your health and maintain an active lifestyle. You'll learn how simple, easy changes in nutrition, fitness, lifestyle and natural supplements can effectively prevent most Cancers and Heart Disease.

You'll receive this total, in-depth evaluation in one day and one place. We'll make you comfortable and look after you every step of the way.

Best of all, you'll get the peace of mind that comes from knowing that you are doing all you can to take care of your health- for yourself and for the people who care about you.

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Learn More About the Exam with Frequently Asked Questions About The Comprehensive Exam

Comprehensive Exam Components

Comprehensive Exam Options and Electives

Find out how to use your Health Savings Account or Flex Account for A Comprehensive Exam

The Road Map

We'll explain the results of your evaluations, provide you with a clear understanding of your health issues and create a detailed, customized treatment plan for you. You'll walk out with a practical "road map" you can follow to maintain and enhance your health and fitness on a daily basis.

At the Princeton Longevity Center, we are your partners in long-term health care. When you walk out of our office, our involvement in your well-being does not end, and we will continue to monitor your progress through a choice of Follow-Up Options. This is not just an exam, it's the start of your plan for staying well for the years to come.

The Rewards

A Comprehensive Exam lets you take control of your health. If you are worried about your risk of heart disease, cancer or other health problems, a Princeton Longevity Center Comprehensive Exam can give you the Peace of Mind that comes from knowing that all is well.

Youll know whether or not you are really at risk for heart attack, cancer, diabetes, premature aging or other significant health issues. And, you will find out what you can do about those risks. You'll learn how to prevent cancer, heart disease, diabetes and many other diseases from affecting your future.

You'll have the opportunity to anticipate and prevent illness and premature aging. You'll learn the simple, easy steps that you can take to prevent cancer, heart attacks, diabetes, lung disease, and more. We will show you how you can improve your nutrition and fitness so that your future years are healthier and more active.

The Princeton Longevity Center is focused on helping you with healthy living at the forefront of new medical knowledge and diagnostic technologies. So, you can stop worrying and know that you are doing all you can to optimize your health for today and the years to come.

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Princeton Longevity Center

Wednesday, October 7th, 2015

Sensation 64-Slice CT High Definition Coronary Artery Scans

I don't want to know if something is wrong. Won't the scan make me too nervous?

What type of scaner is used?

What happens during the scan?

What about the radiation exposure?

How long does a scan take?

Do I need to fast?

Do I need a referral from my physician?

Is the scan covered by my insurance?

How accurate is a Heart Scan?

My cholesterol level is normal. Should I still have a Heart Scan?

What if I already know I have heart disease?

I was told the scan can't detect "soft" plaque. Does that matter?

I already passed a stress test. Should I still have a scan?

How does the scan detect coronary artery disease?

What about blood tests like C-Reactive Protein and Homocysteine?

Is this the same scan that I saw on Oprah or in the newspapers?

What do I do with my test results?

What makes the Princeton Longevity Center's scans different from all the other scanning centers that I have seen or heard advertised?

Request an Appointment or More Information Back to Coronary Artery Scan Page

I don't want to know if something is wrong. Won't the scan make me too nervous?

Heart disease is extremely treatable, especially if found early. If your scan shows that you are at risk for developing coronary artery disease, we can show you how simple changes or treatments can dramatically alter your risk and lessen the chances that you will have a heart attack. Avoiding a scan will not stop the disease. Knowing what simple steps you can take will make a big difference in the quality of the rest of your life.

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What type of scanner is used?

Our scans are done with a Siemens Definition AS 64 Slice CT Scanner. This state of the art scanner uses very low radiation doses and produces exceptional detail, as small as 1/50th of an inch. The scans are also extremely fast, usually less than 10 seconds, so there is no need for prolonged breath-holds. The scanner is completely non-claustrophic.

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What happens during the scan? Is it uncomfortable?

64 Slice CT scans are quick, painless and safe. You lie on a table and hold your breath for a few seconds. There are no needles or dyes; it is not claustrophobic and you usually don't even have to remove your clothes.

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What about the radiation exposure?

There has been a lot of attention in the media surrounding the issue of radiation exposure. We keep our doses as low as possible. Our Coronary Calcium Heart Scans generally involve a dose of about 1 mSv, an amount much lower than is typically cited in the media. According to the US Nuclear Regulatory Commission the risk of 1 mSv is about 1 in 25,000 or, put another way, it raises your cancer risk from 20.000% to just 20.004%. On the other hand, your risk of dying from cardiovascular disease that goes undetected and untreated is 36%. We believe that the potential benefit of early detection of cardiovascular or other diseases more than offsets the extremely small potential risk of this level of radiation exposure.

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How long does a scan take?

The heart, lung or whole body scans take just a few seconds. We will spend some time explaining the procedure to you before the scan. You will get your results within a few mintues. Altogether, you should plan on being at our center about 30 minutes.

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Do I need to fast?

No. There is no special preparation or fasting required for heart, lung or whole body scans.

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Do I need a referral from my physician?

No. While many physicians do refer their patients for these scans, we do not require physician referrals. However, we do encourage you to discuss the test with your physician. With your consent, we will send a copy of your results to your physician along with any recommendations for further treatment or testing.

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Is the scan covered by my insurance?

Most private insurance plans will notcover coronary artery scans . In some cases, the coverage will depend on whether the test is done solely as a preventive screening test or to help your doctor make a decision about your treatment.

Medicare Beneficiaries please note: In general, Medicare does not cover preventive services. Coronary Arteries Scans (CPT Code 75571) are specifically a non-covered service. You will not be able to receive any reimbursement from Medicare for these services.

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How accurate is the Coronary Artery Scan?

It is VERY accurate. There are no false-positives. The presence of calcium in the coronary artery means there is plaque there. The relationship between calcium in the artery and the risk of a heart attack has been well established in numerous medical studies. The more calcium present the higher your risk of a heart attack. The absence of any calcium on your scan means you are not at risk for a heart attack with a 99.9% certainty.

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My cholesterol level is normal so why should I bother with a coronary scan?

Study after study has shown that cholesterol levels do NOT accurately predict who will have a heart attack. In fact, 70% of heart attacks occur in people with "normal" cholesterol levels. Even if your cholesterol level is below the current guidelines you can still develop coronary artery disease. With coronary artery scans we can tell if your current cholesterol level is safe for you or if it needs to be lower.

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What if I already know I have heart disease?

Coronary artery scans are useful not only in early detection of disease but also for following the course of the disease. The scan can be used to monitor your treatment with diet, medication, etc. If your treatment is working, the scan will show the improvement. If it is not working, serial scans can show the continuing progression of the coronary artery disease and alert your physician to the need for more aggressive or alternative treatments.

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I was told coronary artery scans can't detect "soft plaque" and isn't that really where the danger is?

While it is true that a coronary artery scan only shows "calcified plaque" and not "soft plaque" (plaque that has not yet calcified), that does not make the scan any less useful. Calcified plaque serves as a marker for the presence of soft plaque. Numerous studies have proven that the coronary artery scan is the most accurate and sensitive predictor of your risk of having a heart attack or significant coronary artery disease. If you don't have any calcified plaque the likelihood that there is any soft plaque is extremely small. No other non-invasive test can detect the presence of early coronary artery disease as well as coronary scans.

If you have a high level of calcified plaque or your clinical history warrants further investigation, a CT Angiography will very reliably detect the presence of soft plaque and measure whether there is a signficant blockage in the arteries.

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I already passed a stress test. Should I still have a scan?

Stress tests only show an abnormality if you have an artery that is at least 65-80% blocked. At that point, treatment may require surgery or angioplasty. And, 70% of heart attacks happen in arteries that are less than 50% blocked and a stress test would not have shown anything wrong. The coronary artery scan can detect developing blockages much earlier, often many years before anything is detectable on a stress test. At that point, treatment with minor changes in diet and lifestyle along with nutritional supplements or medications can be very effective in preventing any worsening of the disease. That can allow you to avoid surgery or invasive procedures later on.

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How does the scan detect coronary artery disease?

The coronary artery scan detects the presence of calcium deposits in the wall of the arteries. These are often present long before blockages have become severe enough to be found by other means such as stress tests. Coronary artery calcium deposits are a "clinical marker" for coronary artery disease. The more calcium present the higher the risk that you may have a heart attack.

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What about blood tests like C-Reactive Protein or Homocysteine levels? Can't they tell if I have heart disease?

There is currently NO blood test that is able to tell if you have coronary artery disease. Blood tests can only estimate your probability of getting coronary disease. Many people with high levels of cholesterol, C-Reactive Protein or Homocysteine do not have coronary artery disease. At the same time, it is common to still get coronary disease even if those tests are normal. Relying solely on those tests means treating a lot of people who do not actually need to be treated and missing a lot of cases where heart attacks could have been prevented. Coronary scans look directly at your own arteries to see if you have a problem or not. Then, treatment is based on what is actually going on in your arteries instead of a statistical "guess".

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Is this the same scan that I saw on Oprah or in the newspapers?

Yes. 64-Slice CT Scans have been prominently featured on many national talk shows and in numerous magazines and other publications.

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What do I do with my test results?

You will get a copy of your test results along with a detailed explanation of the significance of the restuls immediately after your scan. We strongly encourage you to share these results with your physician to seek his/her advice as to any additional treatment that may be recommended.

Our Full Body Scans include a consultation with one of our expert physicians who will also explain the significance of the heart scan results. If you have a Full Body Scan (either with your heart scan or as part of a Comprehensive Exam) you will also get a preliminary review, pending the final report by our radiologist. If you are referred by your physician, the report will be sent to your physician and further management should be discussed with your doctor. If you are not referred by a physician, the discussion of your scan results will include general guidelines for steps you can take to help lower your future health risks.

Imaging studies and other medical tests may reveal findings that require additional evaluation or treatment. THe Princeton Longevity Center does not offer Primary Care or on-going medical management. All findings related to any tests performed at Princeton Longevity Center should be discussed by you with your Primary Care or Family Physician. If additional testing or treatment is warranted this can be arranged through your personal physician. A copy of your results will be sent to any physician you designate.

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What makes the Princeton Longevity Center's scans different from all the other scanning centers that I have seen or heard advertised?

For cardiac scans, the 64-Slice CT Scanner is the "gold standard." The Princeton Longevity Center is the region's leader in Cardiac Imaging and prevention. We don't just do Cardiac CT, we TEACH it. Our physicians have trained over a thousand physicians from around the world at our renowned Cardiac CT Training Course. Our scans are read twice, including our premier experts in cardiac imaging and radiologists expert in body scans. No other cardiac imaging center in the area offers this level of expertise in the interpretation of your results.

The Princeton Longevity Center is the only scanning center in the region that goes beyond scanning. Our staff of expert physicians, nutritionists and exercise physiologists are available to show you how to take the next step with our Comprehensive Exam program.

After we explain your results to you in-depth, our comprehensive preventive medicine center can offer you the tools and resources you need to immediately start to take a proactive role in your health. We work with you and your family physician to design a plan that will quickly start to lower your risk of heart attack and many other life-threatening diseases.

Other scanning centers may be able to tell you if there is a problem. The Princeton Longevity Center will tell you what you can do about the problem and help you take the next step to a healthier future.

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Product Longevity|Freescale

Wednesday, October 7th, 2015

Microcontrollers Kinetis K K02 - April 2014 Microcontrollers Kinetis K K10 - July 2011 Microcontrollers Kinetis K K11 - August 2012 Microcontrollers Kinetis K K12 - August 2012 Microcontrollers Kinetis K K20 - July 2011 Microcontrollers Kinetis K K21 - August 2013 Microcontrollers Kinetis K K22 - April 2014 Microcontrollers Kinetis K K24 - January 2014 Microcontrollers Kinetis K K26 - May 2015 Microcontrollers Kinetis K K30 - July 2011 Microcontrollers Kinetis K K40 - July 2011 Microcontrollers Kinetis K - K50 July 2011 Microcontrollers Kinetis K - K51 July 2011 Microcontrollers Kinetis K K60 - July 2011 Microcontrollers Kinetis K K63 - January 2014 Microcontrollers Kinetis K K64 - January 2014 Microcontrollers Kinetis K K65 - May 2015 Microcontrollers Kinetis K K66 - May 2015 Microcontrollers Kinetis K K70 - July 2011 Microcontrollers Kinetis L KL02 - June 2013 Microcontrollers Kinetis L KL03 - July 2014 Microcontrollers Kinetis L KL04 September 2012 Microcontrollers Kinetis L KL05 September 2012 Microcontrollers Kinetis L KL13 - 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November 2008 Microcontrollers 8-bit S08 S08FL16 - February 2009 Microcontrollers 8-bit S08 S08SV16 - April 2009 Microcontrollers 8-bit S08 - MC9S08LH June 2010 Microcontrollers 8-bit S08 - MC9S08JE September 2010 Microcontrollers 8-bit S08 - MC9S08MM September 2010 Microcontrollers 8-bit S08 S08GW - January 2011 Microcontrollers 8-bit S08 S08P - November 2011 Microcontrollers 16-bit DSC MC56F8013/14 - April 2005 Microcontrollers 16-bit DSC MC56F802X - August 2007 Microcontrollers 16-bit DSC MC56F8006/2 - March 2009 Microcontrollers 16-bit DSC MC56F803X - July 2009 Microcontrollers 32-bit DSC MC56F84xx - June 2012 Microcontrollers 32-bit DSC MC56F827xx - November 2013 Microcontrollers 32-bit ColdFire MCF521X - September 2005 Microcontrollers 32-bit ColdFire MCF523X - September 2005 Microcontrollers 32-bit ColdFire MCF5207/8 - November 2006 Microcontrollers 32-bit ColdFire - MCF537X January 2007 Microcontrollers 32-bit ColdFire - MCF532X January 2007 Microcontrollers 32-bit ColdFire MCF5253 - February 2007 Microcontrollers 32-bit ColdFire MCF5223x - March 2007 Microcontrollers 32-bit ColdFire MCF51QE128/32 - June 2007 Microcontrollers 32-bit ColdFire MCF521XX - June 2007 Microcontrollers 32-bit ColdFire MCF5445x - September 2007 Microcontrollers 32-bit ColdFire MCF5227x - March 2008 Microcontrollers 32-bit ColdFire MCF51JM - July 2008 Microcontrollers 32-bit ColdFire MCF51AC256 - November 2008 Microcontrollers 32-bit ColdFire MCF5225x - November 2008 Microcontrollers 32-bit ColdFire MCF51CN - March 2009 Microcontrollers 32-bit ColdFire MCF51EM256 - May 2010 Microcontrollers 32-bit ColdFire - MCF5441x September 2010 Microcontrollers 32-bit ColdFire - MCF51JE September 2010 Microcontrollers 32-bit ColdFire - MCF51MM September 2010 Microcontrollers MPC5xxx 32-bit Power Architecture - MPC5125YVN400 April 2010 Processors i.MX Family i.MX233 - August 2009 Processors i.MX Family i.MX25 i.MX25 (Auto) June 2009 Processors i.MX Family i.MX27 - June 2007 Processors i.MX Family i.MX28 i.MX28 (Auto) September 2010 Processors i.MX Family i.MX31 - June 2005 Processors i.MX Family i.MX35 i.MX35 (Auto) October 2008 Processors i.MX Family i.MX50 - July 2011 Processors i.MX Family i.MX51 - November 2009 Processors i.MX Family i.MX53 i.MX53 (Auto) February 2011 Processors i.MX 6 Series i.MX 6UltraLite - September 2015 Processors i.MX 6 Series i.MX 6SoloLite - November 2012 Processors i.MX 6 Series i.MX 6SoloX i.MX 6SoloX (Auto) February 2015 Processors i.MX 6 Series i.MX 6Solo i.MX 6Solo (Auto) November 2012 Processors i.MX 6 Series i.MX 6Dual i.MX 6Dual (Auto) November 2012 Processors i.MX 6 Series i.MX 6DualLite i.MX 6DualLite (Auto) November 2012 Processors i.MX 6 Series i.MX 6Quad i.MX 6Quad (Auto) November 2012 Processors Vybrid Vybrid F Series - June 2013 Processors Vybrid - Vybrid R Series December 2014 Processors QorIQ - LS1020A/22A September 2013 Processors QorIQ - LS1021A September 2013 Processors QorIQ P1010/14 - November 2010 Processors QorIQ P1020/11 - June 2008 Processors QorIQ P1021/12 - December 2009 Processors QorIQ P1022/13 - August 2011 Processors QorIQ P1023/17 - August 2010 Processors QorIQ P1024/15 - December 2009 Processors QorIQ P1025/16 - December 2009 Processors QorIQ P2020/10 - June 2008 Processors QorIQ P2040/41 - May 2011 Processors QorIQ P3041 - June 2010 Processors QorIQ P4040 - September 2009 Processors QorIQ P4080 - June 2008 Processors QorIQ P5020/10 - June 2010 Processors QorIQ P5040/21 - May 2012 Processors QorIQ - T1024 April 2014 Processors QorIQ - T1040/42 October 2012 Processors QorIQ - T2080 June 2012 Processors QorIQ - T2081 October 2012 Processors QorIQ T4160 - February 2012 Processors QorIQ T4240 - February 2012 Processors QorIQ Qonverge BSC9131 - August 2011 Processors QorIQ Qonverge BSC9132 - August 2011 Processors QorIQ Qonverge B4860 - February 2012 Processors Crypto Coprocessors C29x - May 2013 Processors Host Processors MPC7448 - February 2004 Processors Host Processors MPC8641D - September 2004 Processors Host Processors MPC8640D - July 2008 Processors PowerQUICC II Pro MPC8358 - March 2005 Processors PowerQUICC II Pro MPC8360 - March 2005 Processors PowerQUICC II Pro MPC8347 - June 2005 Processors PowerQUICC II Pro MPC8349 - June 2005 Processors PowerQUICC II Pro MPC8321 - May 2006 Processors PowerQUICC II Pro MPC8323 - May 2006 Processors PowerQUICC II Pro MPC8313 - November 2006 Processors PowerQUICC II Pro MPC8314 - September 2007 Processors PowerQUICC II Pro MPC8315 - September 2007 Processors PowerQUICC II Pro MPC8378 - September 2007 Processors PowerQUICC II Pro MPC8379 - September 2007 Processors PowerQUICC II Pro MPC8377 - September 2007 Processors PowerQUICC II Pro MPC8308 - November 2009 Processors PowerQUICC II Pro MPC8306 - March 2011 Processors PowerQUICC II Pro MPC8309 - March 2011 Processors PowerQUICC III MPC8540 - June 2000 Processors PowerQUICC III MPC8541 - July 2001 Processors PowerQUICC III MPC8555 - July 2001 Processors PowerQUICC III MPC8560 - July 2002 Processors PowerQUICC III MPC8543 - September 2004 Processors PowerQUICC III MPC8545 - September 2004 Processors PowerQUICC III MPC8547 - September 2004 Processors PowerQUICC III MPC8548 - September 2004 Processors PowerQUICC III MPC8544 - September 2006 Processors PowerQUICC III MPC8572E - June 2007 Processors PowerQUICC III MPC8610 - September 2007 Processors PowerQUICC III MPC8536 - September 2008 Processors PowerQUICC III MPC8569 - February 2009 Processors 32-bit ColdFire - MCF5251 February 2007 Processors 32-bit ColdFire MCF51JU - March 2012 Processors 32-bit ColdFire MCF51JF - March 2012 Processors 32-bit ColdFire MCF51QU - March 2012 Processors 32-bit ColdFire MCF51QM - March 2012 Auto MCU 16-bit S12 - S12G October 2010 Auto MCU 16-bit S12 - S12HYx October 2009 Auto MCU 16-bit S12 - S12Px July 2009 Auto MCU 16-bit S12 MagniV - S12VR64 December 2011 Auto MCU 16-bit S12X - S12V December 2011 Auto MCU 16-bit S12X - S12XE September 2009 Auto MCU 16-bit S12X - S12XF March 2009 Auto MCU 16-bit S12X - S12XHY December 2010 Auto MCU 16-bit S12X - S12XS September 2009 Auto MCU 16-bit S12 MagniV - S12ZVL January 2015 Auto MCU 16-bit S12 MagniV - S12ZVM March 2014 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5554 July 2004 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5200 March 2005 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5534 June 2005 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5565 February 2006 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5566 May 2006 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5567 December 2006 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5200B September 2007 Auto MCU MPC5xxx 32-bit Power Architecture - MPC567XF October 2008 Auto MCU MPC5xxx 32-bit Power Architecture - MPC564xB-C October 2011 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5676R October 2011 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5777M December 2014 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5121e January 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC563XM January 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC551X September 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC560XB December 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC560xP April 2010 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5668G/E September 2010 Auto MCU MPC5xxx 32-bit Power Architecture - MPC567xK December 2012 Auto MCU 8-bit S08 - S08AWx January 2009 Auto MCU 8-bit S08 - S08LG32 March 2009 Auto MCU 8-bit S08 - S08SGx April 2009 Auto MCU 8-bit S08 - S08ELx September 2009 Auto MCU 8-bit S08 - S08SLx September 2009 Auto MCU 8-bit S08 - S08D November 2009 Auto MCU 8-bit S08 - S08MP16 November 2009 Auto MCU Kinetis EA - EA September 2014 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5553 July 2004 Auto MCU MPC5xxx 32-bit Power Architecture - MPC560xP April 2010 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5645S October 2012 Auto MCU MPC5xxx 32-bit Power Architecture - MPC564xA May 2012 Auto MCU MPC5xxx 32-bit Power Architecture - MPC564xL October 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC564xS May 2012 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5668G July 2012 Auto MCU MPC5xxx 32-bit Power Architecture - MPC567xK December 2012 DSP 24-bit DSP DSP56311 - October 2004 DSP 24-bit DSP DSP56321 - February 2005 DSP 24-bit DSP DSP56720 - May 2008 DSP 24-bit DSP DSP56721 - May 2008 DSP 24-bit DSP DSP56724 - August 2008 DSP 24-bit DSP DSP56725 - August 2008 DSP StarCore DSPs MSC8122 - May 2005 DSP StarCore DSPs MSC8156 - November 2008 DSP StarCore DSPs MSC8154 - April 2010 DSP StarCore DSPs MSC8252 - April 2010 DSP StarCore DSPs MSC8254 - April 2010 DSP StarCore DSPs MSC8256 - April 2010 DSP StarCore DSPs MSC8251 - April 2010 DSP StarCore DSPs MSC8151 - June 2010 DSP StarCore DSPs MSC8152 - June 2010 Sensors Accelerometer - MMA3201 January 2000 Sensors Accelerometer - MMA3202 January 2000 Sensors Accelerometer - MMA3204 January 2000 Sensors Accelerometer - MMA2201 May 2000 Sensors Accelerometer - MMA2202 May 2000 Sensors Accelerometer - MMA2204 May 2000 Sensors Accelerometer - MMA2301 May 2000 Sensors Accelerometer - MMA1254 May 2002 Sensors Accelerometer - MMA1260 November 2003 Sensors Accelerometer - MMA1270 November 2003 Sensors Accelerometer - MMA62xx June 2006 Sensors Accelerometer - MMA65xxKW November 2011 Sensors Accelerometer MMA766X - April 2009 Sensors Accelerometer MMA8451Q - February 2010 Sensors Accelerometer MMA8452Q - February 2010 Sensors Accelerometer MMA8491Q - February 2011 Sensors Touch Sensors MPR031 - February 2009 Sensors Touch Sensors MPR121 - December 2009 Analog Audio SGTL5000 - June 2008 Analog Battery Sensor - MM912_637 February 2011 Analog Communication Transceiver - MC33660 October 2011 Analog Embedded Microcontrollers + power - MM908E626 September 2004 Analog Embedded Microcontrollers + power - MM908E624 November 2004 Analog Embedded Microcontrollers + power - MM908E622 September 2005 Analog Embedded Microcontrollers + power - MM912_634 September 2010 Analog Embedded Microcontrollers + power - MM912F634 October 2010 Analog eXtreme Switch - MC33981 (MC12XS2) August 2004 Analog eXtreme Switch - MC33982 (MC12XS2) July 2006 Analog eXtreme Switch - MC33984 (MC12XS2) July 2006 Analog eXtreme Switch - MC10XS3412 October 2008 Analog eXtreme Switch - MC10XS3435 October 2008 Analog eXtreme Switch - MC15XS3400 October 2008 Analog eXtreme Switch - MC35XS3400 October 2008 Analog eXtreme Switch - MC33988 (MC12XS2) August 2010 Analog eXtreme Switch - MC10XS3535 August 2010 Analog eXtreme Switch - MC35XS3500 August 2010 Analog eXtreme Switch - MC09XS3400 March 2012 Analog eXtreme Switch - MC06XS3517 March 2012 Analog eXtreme Switch - MC10XS4200 (MC24XS4) June 2012 Analog eXtreme Switch - MC20XS4200 (MC24XS4) June 2012 Analog eXtreme Switch - MC06XS4200 (MC24XS4) September 2012 Analog H-bridge - MC33887 September 2006 Analog H-bridge - MC33932 January 2009 Analog H-bridge - MC33931 March 2009 Analog H-bridge MC34931 - January 2015 Analog H-bridge MC34932 - January 2015 Analog H-bridge - MC33926 May 2009 Analog H-bridge MC34933 - July 2010 Analog L/HS Switch - MC33879 December 2006 Analog LED Driver MC34844 - October 2008 Analog LED Driver MC34845 - June 2009 Analog LED Driver MC34848 - June 2010 Analog LIN Physical Layer - MC33662 September 2011 Analog LIN physical Layer - MC33663 August 2012 Analog Linear Regulator - MC33730 March 2009 Analog Power Management and user interface MC13783 - April 2006 Analog Power Management and user interface MC13892 - April 2010 Analog Power Management and user interface MC34708 - November 2011 Analog Power Management and user interface - MC34VR500 October 2014 Analog Power Management and user interface MMPF0100 MMPF0100 (Auto) October 2012 Analog Power Management and user interface MMPF0200 MMPF0200 (Auto) February 2014 Analog Powertrain and Engine Control - MC33810 July 2007 Analog Powertrain and Engine Control - MC33800 July 2007 Analog Powertrain and Engine Control - MC33811 July 2008 Analog Powertrain and Engine Control - MC33812 August 2009 Analog Powertrain and Engine Control - MM912_P812 July 2012 Analog Powertrain and Engine Control - MC33816 April 2014 Analog Pre-Drivers - MC33937 June 2008 Analog SBC - MC33989 November 2002 Analog SBC - MC33742 January 2004 Analog SBC - MC33742 June 2008 Analog SBC - MC33910 March 2009 Analog SBC - MC33911 March 2009 Analog SBC - MC33912 March 2009 Analog SBC - MC33904 November 2009 Analog SBC - MC33905 November 2009 Analog SBC - MC33903 March 2011 Analog SBC - MC33907 April 2014 Analog SBC - MC33908 April 2014 Analog Switch Detection Interface - MC33978 January 2015 Analog Switch Detection Interface MC34978 - February 2015 Analog Signal Conditioning - MC33975 February 2005 Analog Signal Conditioning - MC33972 July 2006 Analog Switching Regulator MC34712 - April 2007 Analog Switching Regulator MC34713 - April 2007 Analog Switching Regulator MC34716 - April 2007 Analog Switching Regulator MC34717 - April 2007 Analog Switching Regulator MC34704 - March 2008 Analog Switching Regulator MC34700 - April 2008 RF Land Mobile - AFT09MS031N April 2012 RF Land Mobile - AFT05MS031N April 2012 RF Land Mobile - AFT05MP075N January 2013 RF Land Mobile - AFT09MS007N June 2013 RF Land Mobile - AFT09MS015N December 2013 RF Land Mobile - AFT09MP055N July 2013 RF Land mobile - AFT05MS004N June 2014 RF RF Military MMRF1004N - December 2013 RF RF Military MMRF1005H - December 2013 RF RF Military MMRF1006H - December 2013 RF RF Military MMRF1007H - December 2013 RF RF Military MMRF1008H - December 2013 RF RF Military MMRF1009H - December 2013 RF RF Military MMRF1012N - February 2014 RF RF Military MMRF1014N - March 2014 RF RF Military MMRF1015N - March 2014 RF RF Military MMRF1016H - February 2014 RF RF Military MMRF1019N - March 2014 RF RF Military MMRF2004NB - December 2013 RF RF Military MMRF2005N - October 2014 RF RF Military MMRF2006N - April 2014 RF RF Military MMRF2007N - October 2014 RF RF Military - MMRF2010N June 2015 RF RF Military - MMRF5014H December 2014 RF RF Military - MMRF1020-04NR3 January 2014 RF RF Military - MMRF1304N December 2013 RF RF Military - MMRF1304L December 2013 RF RF Military - MMRF1305H December 2013 RF RF Military - MMRF1306H December 2013 RF RF Military - MMRF1308H March 2014 RF RF Military - MMRF1310H March 2014 RF RF Military - MMRF1315N June 2014 RF RF Military MMRF1316N - June 2014 RF RF Military - MMRF1318N June 2014 RF RF Military - MMRF1320N March 2015 RF RF Power Products - AFIC10275N November 2014 RF RF Power Products - MRF6V2150N February 2007 RF RF Power Products MRF6VP41KH - December 2007 RF RF Power Products - MRF6V14300H September 2008 RF RF Power Products - MRF6V12250H May 2009 RF RF Power Products - MRF6V12500H August 2009 RF RF Power Products MRF6VP121KH - December 2009 RF RF Power Products - MRFE6VP6300H October 2010 RF RF Power Products - MRFE6VP61K25H November 2010 RF RF Power Products - MRFE6VP5600H December 2010 RF RF Power Products - MRF8P29300H February 2011 RF RF Power Products - MRFE6VP8600H September 2011 RF RF Power Products - MRFE6VP100H April 2012 RF RF Power Products - MRFE6VS25N May 2012 RF RF Power Products - MRFE6S9060N/GN March 2007 RF RF Power Products - MRFE6VP5150N June 2014 RF RF Power Products - MRFE6VP5300N June 2014 RF RF Power Products - MRFE6VP61K25N February 2015 RF RF Power Products - MRF8VP13350N May 2015 RF RF Power Products - MRF7S24250N September 2015 Analog Power Management and user interface PF3000 - Jun 2015

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Product Longevity|Freescale

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Princeton Longevity Center Review – Health care center …

Monday, October 5th, 2015

Princeton Longevity Center Information

Princeton Longevity Center helps you prevents cancers and heart attacks, live longer, look and feel younger. Medicine has changed dramatically in the last forty years. Therefore, why are you still relying on your father's annual physical to stay well.

Services of Princeton Longevity Center

Our healthcare center provides state-of-the-art diagnostic facilities and a level of personal time, care and attention that is unmatched. Our healthcare center also offer a wide array of programs designed to meet the unique needs of busy corporate executives.

Our healthcare center equipped modern equipment such as 4-Slice CT Heart Scans and 3-D Virtual Colonoscopy our exams are able to detect the earliest evidence of the leading causes of death and disability years before any other tests. This will help our healthcare center to identify early and find appropriate treatment for you.

In addition, the best of all, while the Princeton Longevity Center's Executive Exams are the most comprehensive and effective you can find, we are also the most cost-effective. We commit that you will satisfied about cost and service while treatment

Contact Information

Center Name: Princeton Longevity Address: 136 Main Street, Forrestal Village Princeton, New Jersey 08540 Phone Number: 888-8000-PLC (toll-free) or (888.800.0752) Website: http://www.theplc.net Working Hours: For more information call (888.800.0752) or fax (609)430-8470

If you are unsatisfied about this center you can refer toHealth Care District of Palm Beach County. Read moreHealth Care District of Palm Beach County Reviews here.

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Princeton Longevity Center Review - Health care center ...

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Longevity for You

Monday, October 5th, 2015

A holistic approach to autoimmune diseases! Click here for more information.

Stephen Lau

For more information, click here.

Longevity is the quest of many individuals. To live a long life and yet remain physically, mentally, and spiritually healthy is a challenge requiring great wisdom.

A long lifespan is a blessing, which has to be earned with the wisdom of an anti-aging healthy lifestyle.

Your Creator has given you the innate wisdom to live long, and your mission in life is to earn those extra years.

The objective of this site is two-fold:

To share with you my own experience of an autoimmune disease, and my self-awakening from that experience.

To share with you my search for health information on natural healing and

My mission is to provide you with

Your mission is to earn those extra years through a healthy longevity mindset to live an anti-aging and lifestyle. Longevity is for you, if, indeed, it is your passionate quest in life.

This is not a mission impossible: if there is a will, there must be a way.

You will be imbued with passion to live a longer tomorrow by changing not only your attitudes but also your lifestyle through a wealth of health information to accomplish your mission to earn your extra years.

Yes, the road to longevity may be long and winding, and even bumpy at times. But you need not fasten your seat-belt to the past or to the present (whatever the state of health you may be currently in). Rest assured, this site will continue to update you with new health information needed to earn your extra years. At the end of t-he day, you will be proud of yourself that you have a credential of living long that few would even dare to contemplate.

Stephen Lau

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Longevity for You

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