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Why fasting can help, or hurt, your chances of longevity and weight loss – WRVO Public Media

August 19th, 2017 7:41 am

Not eating, deliberately, has been a way to make a political statement for centuries. And for even longer, its been a normal part of some religious practice. But far more recent uses of fasting are for weight loss and other health benefits -- scientifically proven benefits like lowered cholesterol and reducing systemic inflammation.

Dr. Valter Longo joins us on Take Care this week to discuss the benefits, challenges and problems associated with fasting. Longo is a professor of gerontology and biological science at the University of Southern California Leonard Davis School of Gerontology. Hes also director of the USC Longevity Institute.

There are three major fasting practices, according to Longo.

Short term effects of fasting

When you begin to fast, your body makes a metabolic switch.

There is no more sugar basically coming into the body, Longo says. "There are no more proteins coming in, so the body switches from a mode in which carbohydrates are the main source of fuel to fats. So the body starts breaking down the fats.

Autophagy can also occur, where cells start to destroy themselves, only to replace them later.

Theres also breaking down of entire cells, so killing of entire cells, and then eventually the regeneration of the cells that have been killed during fasting when we return to the normal food, Longo says.

Long term effects of fasting

Longo says the idea of fasting should be respected, because it has large consequences. He says that within just five days of fasting the brain switches from using just sugar to make fuel to using both sugar and ketone bodies at a 50:50 ratio.

Just like you dont take drugs because they worked for someone else, you shouldnt try fasting without the guidance of a medical practitioner, Longo says. Water only fasting, for example, should only be attempted at a clinic with nurses and doctors on staff.

Longo does cite fasting-mimicking diets as a safe way to achieve positive, long-term effects (diets that mimic fasting usually allow you to eat between 100 and 750 calories per fasting day). These effects include:

What you can do

Keeping in mind compliance, I would say there are three major things that can be done, Longo says.

He says for those who have problems with weight, the first two options are best. Time restrictive eating is a good option for many people, allowing them to eat for a certain period of time, say 12 hours and then restricting eating for the following 12 hours.

Most people can do it. Most people around the world who get to 100 years of age -- that was normal [for] them, Longo says.

Another option is to just cut back on the number of meals you eat per day, he says.

You can go from lets say three, four, five, six meals a day, reduce it to two major meals per day and one snack, Longo says If you look around the world, its very common for people to have two meals a day.

A periodic fasting mimicking diet also can reap most of the benefits associated with the practice. A normal, healthy person, who exercises regularly can eat a restricted calorie diet of 750 to 1,100 calories a day for five days in a row, according to Long0, and can do this once or twice a year.

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Diet diary: From Andes to Japanese islands, lessons in longevity – The Indian Express

August 19th, 2017 7:41 am

Written by Ishi Khosla | Published:August 19, 2017 2:23 am Scientific studies and research have shown that besides genetic factors, longevity is strongly linked to food and exercise habits.

Immortality is impossible but living a long life isnt. Some cultures like the Vilcabambans of the Ecuadorian Andes, the Hunza of Pakistan and the centenarians of the Okinawa island in Japan are known for their long lives and may help scientists dealing with life expectancy.

Okinawa, for instance, is home to the worlds healthiest elderly with the longest recorded life expectancies. Scientific studies and research have shown that besides genetic factors, longevity is strongly linked to food and exercise habits.

Low-calorie healthy diets and high physical activity in these extraordinarily healthy societies are the secrets for their extended lifespans with virtually no reported incidence of diseases like high blood pressure, heart disease, cancer, diabetes and other degenerative diseases such as rheumatism, osteoporosis, Alzheimers and vision problems.

So what are the dietary secrets to longevity? Eating less has been found to be critical and seems to be the centrepiece of longevity. In animal experiments, researchers have demonstrated that calorie restriction has now been clearly proven to be effective and up to 30 per cent calorie restriction leads to extended years in a manner believed to be similar to genetic modification. Additionally, high intake of vegetables, fruits, whole grains, soy, fish and eating less fat along with healthy lifestyle seems to explain protection from diseases and increased lifespan.

A study reported that healthy older Okinawans eat an average of seven servings of vegetables, seven servings of whole grains, two servings of soy products; fish twice or thrice a week and very little sugar and added fats. Their diets include little meat and no margarines, hydrogenated fats or trans fat.

Although the impact of good nutrition on health and disease begins very early in life, its never too late to make changes. According to researchers, at age 65 men and women in high- income countries still have a life expectancy of a further 15 and 19 years respectively. The older one becomes, the longer one is likely to live, and thus, by the time men and women reach age 75, life expectancy is still 9 and 11 years, respectively. This dispels the common assumption that changes in lifestyle to improve health are no longer worthwhile in old age. In fact, the prevalence of heart disease, diabetes, hypertension, obesity and arthritis is highest in the older population. Studies demonstrate that it is still worthwhile for older people to make lifestyle changes like diet modification, weight reduction, sodium restriction, saturated fat restriction smoking cessation and that these changes make life in later years healthier, more active and less dependent.

Clearly, living long is not a coincidence. It is a result of many factors and when it comes to health and longevity, the sum of the dietary components is greater than its individual elements. The important thing to be remembered is that these scientifically proven secrets of the worlds healthiest and long-lived people are simple to say the least. Adopting them with common sense can certainly extend your later years with vibrancy and vitality.

Super-centenarian diet

* Eat less and eat well- low calories and nutrient dense foods.

*Choose a diet particularly rich in phyto-chemicals (antioxidants), vitamin B6, B12, folic acid, zinc, calcium, iron, chromium, vitamin D & E and omega-3 fats.

* Eat good carbohydrates, good fat, high-quality proteins and fibre.

* Include plenty of whole grains, fruits and vegetables into your dietary plans.

*Include protein-rich foods such as fish, soy, legumes peas and beans, seeds, nuts, fermented milk products, buttermilk & fermented foods.

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Putting off retirement may benefit your brain, health, and longevity – Harvard Health

August 19th, 2017 7:41 am

The purpose and engagement of a job you love can keep you healthy and connected.

Published: September, 2017

Image: monkeybusinessimages/Thinkstock

While many women dream of kicking back and relaxing into retirement, there's increasing evidence that in some cases, it's better for your brain and your health to keep your nose to the grindstone a little longer.

"The research to date is mixed, but it tends toward the positive that is, for many people, there are health benefits to working longer," says Dr. Nicole Maestas, associate professor of health care policy at Harvard Medical School.

The right job, she says, can keep you connected socially; it can help you stay physically active; and it can give you a purpose, a challenge, or a creative outlet. These factors have all been shown to contribute to health over the long term.

One 2016 study in the Journal of Epidemiology and Community Health suggests that retiring early may actually increase your risk of dying early. Findings showed that healthy people who postposed retirement and chose to retire a year later than those in a comparison group had an 11% lower risk of dying from any cause during the study period (1992 to 2010). Retirees with health problems also lived longer when they postponed retirement. Another study, by the French government's health research agency, linked a later retirement to a reduced risk of Alzheimer's disease and other forms of dementia.

Working longer may also help you retire more comfortably when you do decide it's time. Women who stay on the job longer can earn back income lost during breaks they took earlier in their careers. In one recent study, Dr. Maestas found that women gain more financial return than men do from continuing to work through their 50s and 60s. "And it has the added benefit of boosting their Social Security benefits," she says.

However, it's important to note that while the research may be leaning in favor of working longer for better health, not all studies show benefits or even a connection. In a study in the Journal of Health Economics, Australian researchers concluded that it's actually your overall health not your retirement agethat affects longevity.

The variation in findings may reflect two challenges inherent in this area of study. First, it's difficult for researchers to determine which came first, health problems or retirement. "While work may affect your health, at the same time your health affects your ability to work," says Dr. Maestas. A second challenge is that existing research has studied the effects of retirement on different groups of people. Some may benefit from retiring sooner, others from working longer. "Researchers haven't figured out yet who gets the benefits and who doesn't," says Maestas.

These mixed findings make sense when you think about how the job you do and the environment you work in can influence your health. While a positive work environment may improve your health, the opposite may be true for women who work in hostile environments that cause them physical or psychological stress, involve physical risks, or are monotonous and uninspiring, says Dr. Maestas. "So, if there is one message to women, it is to continue to work if you experience the work environment in a positive way; otherwise, you might consider transitioning to a new positionperhaps even within the same company," she says.

The good news is that today women have more flexibility than ever when mulling whether to retire or stay at work a few years longer. "One helpful trend in this regard is that 'retirement' is no longer an all-or-nothing decision like it used to be," says Dr. Maestas. In some cases, women reshape their jobs rather than leave them altogether. "Many people reduce hours, change jobs, downshift to less demanding positions, or change occupations. Some people take short breaks to reboot skills or take a trip," says Dr. Maestas. "Some people will later upshift for a period of time if a great opportunity comes along. They may even start a business."

Ultimately, for most women, the decision about when to retire will depend on a variety of considerations, from family needs to health and future plans. "But it is worth placing more weight on the long view working longer can enhance financial security and, under some circumstances and for some people, may even boost your health," says Dr. Maestas. "In my opinion, women should try to maintain engagement in the workforce for as long as possible."

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Longevity Lifestyle Preparation: What advisors need to know to prepare female clients for living well to and through … – InvestmentNews

August 19th, 2017 7:41 am

« Back to Webcasts Index

Featuring Mary Beth Franklin from InvestmentNews

Your clients are living longer and spending more time in retirement than ever before especially female clients, who often outlive their spouses or partners.

This live, interactive webcast will arm you with strategies and data for understanding your female clients' life expectancies as well as their retirement and financial scenarios. Research from Great-West Financial in collaboration with the Stanford Center on Longevity focused on how you can incorporate longevity planning into your practice will also be presented.

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Featuring Mary Beth Franklin from InvestmentNews

Your clients are living longer and spending more time in retirement than ever before especially female clients, who often outlive their spouses or partners.

This live, interactive webcast will arm you with strategies and data for understanding your female clients' life expectancies as well as their retirement and financial scenarios. Research from Great-West Financial in collaboration with the Stanford Center on Longevity focused on how you can incorporate longevity planning into your practice will also be presented.

Attendees may submit questions before and during the live event. This free and invaluable resource will help you, your current clients and prospects.

Sponsored by:

Continuing Education Credits: For all webcasts approved for CE credit by the CFP Board, credit will be reported one week after the live event. For on-demand viewers, CE credit will be reported 30 days after the live event. After 30 days, webcasts are available until December 31 in the calendar year for on-demand viewing and are not eligible for CE credit.

For all webcasts approved by IMCA for CIMA/CIMC/CPWA CE credits, email info_cecredits@investmentnews.com for the IMCA program ID to self-report for CE credit. Program IDs will be provided up to 30 days after the live event. After 30 days, webcasts are available until December 31 in the calendar year for on-demand viewing and are not eligible for CE credit.

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Voices The role of advisors in longevity planning – Financial Planning

August 19th, 2017 7:41 am

Perspective and timing is everything.

In 1930, five years before Social Security legislation was passed, the average life expectancy of U.S. citizens was 59.7 years. Thus, the math worked out somewhat favorably for a program designed to pay workers a continuing income after retirement at age 65. The number of people who could statistically expect to live long enough to actually collect was pretty limited, and the percentage of people older than 65 was less than 6%.

What it means to be elderly has undergone a dramatic shift.

Today, those aged 65 and above make up around 12% of the U.S. population. That number is expected to hit 19% by the year 2030. And the average life expectancy in the US has gone up to almost 80 years.

Our perspective on what it means to be elderly has undergone a dramatic shift. Indeed, the World Health Organization estimates that a typical 60-year-old today can reasonably expect not only to survive for many more years, but also to enjoy a healthy, active lifestyle for two decades or more. As technology and medical science continue to advance, we may soon receive a longevity dividend of 30 or even 40 years beyond that available to our great-grandparents. Some researchers even suggest that half of the babies born in todays industrialized countries will live to an age of 100.

When 80 becomes the new 60Think about this prospect: The seniors of the future are likely to enjoy two, three or even four decades of life beyond what we now consider retirement age. What possibilities does this open up? Will it change the way we think about work? About education? About health care?

Another factor to consider is that the baby boomers entering retirement today are more educated, more technically savvy and more connected to the information universe than any prior generation of retirees. They are accustomed to asking questions, looking things up and digging for answers. They also have more information available to them than ever before. A recent Merrill Lynch study reported, for example, that boomers were four times more likely to do their own research on health matters than their parents. These retirees want more than just access to expertise; they want to participate in evaluating the data relevant to their decisions.

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For clients considering long-term care options, a move may be appealing if they find care options in other states that can help them save down the road.

Joseph Coughlin, director of MITs AgeLab, suggests that increasingly, people entering retirement are outcome-focused. Employing a metaphor first suggested by marketing theorist Theodore Levitt, Coughlin says that more and more, retirees just want the tools needed to accomplish the goals they desire. They dont want to own a drill because they want to have a drill around the house; what they really want is a tool to create hole in the wall.

Similarly, boomers dont really want stocks, bonds, mutual funds or insurance; they want the means to live their desired lifestyle when they are no longer actively employed. They want to solve the problems that come with longevity, and those problems, more and more, go beyond simply funding their retirement accounts.

Use the right toolsThe key to longevity planning, then, is to be positioned as a provider of the necessary tools. Consider some of the problems that todays retirees will face:

In order to position themselves to adequately respond to the longevity needs of an aging clientele, advisors will increasingly be called upon to provide not just transaction-based assistance, but also to serve as facilitators of the relationships required to address these and other problems. We will fall short helping our aging clients if we stay in our financial silos; instead, we will need to become conduits for leading them to the solutions they require.

Financial advisors now stand at a frontier: the new business of longevity, says Joseph Coughlin, president of MITs AgeLab.

Certainly, it isnt reasonable to expect advisors to also become experts in gerontology, physical therapy, or occupational counseling. Our deep knowledge of our clients situations and our ability to help them make wise choices about their financial resources will continue to be crucial. We must still be their tool for the important job of maintaining financial security.

But as the longevity trend continues, our clients will need other tools as well. Working from the foundation of our commitment to know them thoroughly, we can provide vital connections for our clients to the other tools they will need. We can form relationships with trusted, thoroughly vetted professionals in industries including housing, construction, home care and employment to help them and their children solve their problems. As AgeLabs Coughlin notes, Financial advisors now stand at a frontier: the new business of longevity. That business will provide them with opportunities to engage with their clients over a lifetime, on more topics, more often, and with greater intimacy.

In many ways, this is the logical extension of the financial advisors mantra of Know your client. As our clients travel farther down the road of the longevity revolution, it will be up to us advisors to help keep their vehicle in top running condition.

Kimberly Foss, CFP, CPWA, is a Financial Planning columnist and founder of Empyrion Wealth Management in California and New York. Shes also the New York Times best-selling author of Wealth by Design. Follow her on Twitter at @KimberlyFossCFP.

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Friday the 13th’s Longevity is More Than Just This 80s Bikini – Game Revolution

August 19th, 2017 7:41 am

As with any popular multiplayer game, the community of Friday the 13th: The Game is a passionate one, and passionate communities are quick to express that passion, be it laudatory, constructive or even outright negative. Just a few weeks ago, when fans figured out that IllFonic, one of the game's two development teams, was also working on another game, they were quick to doom and gloom how they had abandoned Friday the 13th.

Of course, this wasn't the case, and IllFonic released a strongly worded statement to that effect, but anyone who still wasn't convinced should be more than satisfied by yesterday's series of announcements regarding Friday the 13th, including a clothing pack, a new full-size map, new counselors and new playable Jasons. But, for the first time since release, Friday the 13th: The Game has revealed a strategy for longevity that is about more than just the frills (even though the frills in this case are particularly easy on the eyes).

Yes, many people will be more than satisfied with the announcement of the Spring Break 1984 clothing pack, which features in its header image the counselor Tiffany in an unbelievably skimpy bikini. When I first saw this image, I assumed it was a fan-made joke, and then I assumed that bikini's in the 1980s couldn't have possibly looked like that. Of course, I was wrong on both assumptions. But as eye-popping as these new counselor outfits may be, we've gotten new outfits before in Friday the 13th: The Game. As an apology for launch issues, they released a Retro Jason Skin, and a new clothing pack with two new outfits for each counselor.

That said, this particular counselor skin is certainly capturing the cheesier tropes of the 80s horror movie, with the scantily clad counselors being killed by Jason Voorhees. But again, these are just frills, and they won't sustain a game by themselves. But this upcoming update, for several reasons is much different than Content Update 1. Beyond just visuals, the upcoming changes will actually enhance how we play and enjoy Friday the 13th: The Game.

You have to mention the new counselors, which, if handled correctly, should each bring a new playstyle to the table, offering new strategies to which players will have to adjust. Likewise, the new playable Jason should feel like he brings his own strengths and weaknesses to the table. Meanwhile, all of these strategies can play out on the upcoming new full map. But, more than anything else, you have to admire Gun Media's and IllFonic's continued commitment to improving stability.

While their lack of expediency in this matter has frustrated even the most devoted fans, it's nice to know that it's still happening. Better yet, Gun Media nearly fully detailed the upcoming patch that purports to fix several game-ruining bug fixes, such as key objects falling through the ground upon death and ensuring Perks that start you with items actually work (imagine that). Sure, we don't know the timeline just yet, but when have we ever been able to nail Friday the 13th: The Game to a specific date? Beyond that, it's just refreshing to see that the future of Friday the 13th is secure and goes beyond superficial additions (sexy, though they may be).

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Ask SAM: How will Winston-Salem Open handle eclipse? | Ask SAM … – Winston-Salem Journal

August 19th, 2017 7:41 am

Q: With the solar eclipse looming Monday afternoon, I notice the Winston-Salem Open is scheduled to start play at 3 p.m. Are any adjustments being considered for the players participating at that time?

Answer: Play will go on as normal, according to organizers of the Winston-Salem Open. The eclipse will start at 1:12 p.m., reach its maximum at 2:41, and end at 4:03 p.m. But there will be some special commemorations of the event at the Open:

Q: If someone normally wears vision glasses, do the eclipse safety glasses go over, or under, your glasses, or should no other glasses be worn at all? I havent seen this addressed anywhere. What is the protocol for eyeglass wearers?

Answer: If you normally wear eyeglasses, keep them on while wearing eclipse glasses put eclipse glasses on over them, said Dr. Rajiv Shah, assistant professor of opthalmology at Wake Forest Baptist Medical Center.

Its also important to note that even when wearing eclipse glasses, you should not look at the sun through a camera, telescope, binoculars or other optical device. The concentrated solar rays will damage the filter and enter the eyes, Shah said.

He added that you should always supervise children using solar filters and inspect the glasses before use. If the glasses are scratched, punctured, torn or otherwise damaged, they should be discarded.

And to repeat a frequent warning: Dont try to use ordinary sunglasses, even very dark ones. Wear solar eclipse glasses and use handheld solar viewers that are compliant with the International Organization for Standardizations ISO 12312-2 standard. Failing to use proper precautions could lead to irreparable eye damage.

And dont wear eclipse glasses while driving.

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Eclipse safety glasses hard to find in Capital Region – The Daily Gazette

August 19th, 2017 7:41 am

People can't look at Monday's solar eclipse without solar eclipse glasses.

This weekend, sun and moon lovers may look all over the Capital Region for the safety-tested, black-filmshades.

But they will have trouble finding them.

Stores have exhausted their supplies. There were none at Toys "R" Us in Clifton Park, none at Wal-Mart in Amsterdam, none at Lowe's in Glenville.

Lowe's in Niskayuna -- no. Walmart in Rotterdam -- no. Local hardware stores -- no.

"We are all sold out," said one store representative on Friday. "Every store around is sold out."

Places all over the country have sold out. And online sales may now be tricky;even rush orders may not arrive by early Monday afternoon, when the "Great American Eclipse" will begin.

The rare event will darken skies from Oregon to South Carolina along a 70-mile stretch. People in the "path of totality" will see the moon completely block the sun and cast a shadow on the surface of the Earth.

In the Capital Region, astronomy fans will see a partial eclipse -- 66 percent of the sun will be covered by the moon. The show will start at 1:22 p.m. and end at 3:56 p.m. The best time to check out the cosmic conference will be about 2:45 p.m.

Libraries around the U.S. have the shades, whichresemble old-fashioned, 3-D movie glasses. According to the American Astronomical Society, 6,900 libraries have been given solar eye wear through a program supported by NASA, Google and the Gordon and Betty Moore Foundation.

At the Schenectady County Public Library's eclipse gathering, which begins at noon and runs until 4 p.m., glasses will be available outside the building. People who attend the library party won't even have to examine the heavens to see the lunar-solar team-up; a live NASA stream of the celestial event will be held in the McChesney Room.

The glassessold out at miSci -- Schenectady's Museum of Innovation and Science. Valerie Rapson, outreach astronomer at the Dudley Observatory at miSci, said the museum's gift store had nearly 4,000 pairs in stock.

People must have the protection if they'regoing to watch the skies. Sunglasses with tough-sounding names such as "Solar Shields" are not going to work. They will not be safe.

The American Optometric Association added that smoked glass, unfiltered telescopes or magnifiersand polarizing filters will also be unsafe for eclipse viewing.

The American Academy of Opthalmology has also issued a warning:"Looking directly at the sun, even while it's partially eclipsed, can permanently damage vision or blind you."

According to Rapson, "The special glasses block 99.99 percent of the light, which is way more than a regular pair of sunglasses. That's the main thing to stress. Sunglasses are not enough. They really have to have those safety glasses."

The eclipse glasses must come from reputable vendors -- theAmerican Astronomical Society has composed a page of legitimate manufacturers and authorized dealers of eclipse glasses and handheld solar viewers, all verified to be compliancewith the ISO 12312-2 international safety standard.

Angela Strong, assistant library director for operations at the Schenectady County Public Library, is expecting a large crowd for the eclipse party. She said glasses will be distributed outside the building, with a limit of four pairs per family.

"We're going to encourage people to share the glasses," Strong said. "It's recommended people limit their viewing to three minutes at a time."

People without glasses at miSci will be able to "watch" the show with "sun spotters," devices that will project images of the sun on white paper. Telescopes equipped with safe solar filters will also be on the grounds.

Reach Gazette reporter Jeff Wilkin at 395-3124 at at wilkin@dailygazette.com or @jeffwilkin1 on Twitter.

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Eclipse safety glasses hard to find in Capital Region - The Daily Gazette

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Shire PLC (SHP): Looking To Captalise On Unmet Needs In Eye Care – Simply Wall St

August 19th, 2017 7:41 am

Irish biotech giantShire plc (LON:SHP) received a validation fromthe UK, in the capacity of the Reference Member State, for its marketing authorization application forlifitegrast. If approved, lifitegrast would be the first and only treatment in a new class of drugs (LFA-1 antagonist) to address the signs and symptoms of dry eye disease in adults in Europe, said the company.

Shire submitted the application for marketing authorization (MAA) through a Decentralized Procedure toDenmark, Norway, Sweden, Finland, the UK, Germany, the Netherlands, France, Italy, Portugal, Spain and Greece.This submission is another important milestone for lifitegrast and the millions of patients living with dry eye disease, which can impact a persons vision-related quality of life, affecting daily activities such as reading and using computers, commented Shires head of clinical department Howard Mayer.

Opthalmology hasnt been at the core of Shires growth agenda historically, but its acquisition of SARcode Bioscience in 2013 marked an official entry into the medical field, where Shire expects to capitalise on unmet needs in eye care through a multi-faceted approach targeting rare diseases and specialty conditions.

Shires MAA forlifitegrast is backed by what the company claims to be the largest development program to date for an investigational stage dry eye disease candidate. The program involves five clinical trials with 2,500 patients. In four safety and efficacy studies, lifitegrast improved symptoms as measured by patient reported eye dryness score (EDS), and in three of the four studies improved the objective signs of dry eye disease (measured using corneal staining), said Shire.

Nearly a year ago, llifitegrast received the US FDA approval as Xiidra for dry eye treatment. Out of more than US$14 billion in sales over the past year, Xiidra accounted for just over $50 million (representing a more than 20% market share in the US) with opthalmology contributing 2% to overall sales, which largely comprises of five therapeutic areas: Hemtology, Genetic Diseases, Immunology, Neuroscience and Internal Medicine.

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Bangladesh successfully reduces child blindness over the last 14 years – Dhaka Tribune

August 19th, 2017 7:41 am

Bangladesh has successfully reduced around 50% of child blindness in last the 14 years, which has come down to 25,000 from 48,000 as estimated in the year 2000.

Dr AHM Enayet Hussain, head of paediatric ophthalmology at the National Institute of Opthalmology and Hospital and program manager of national eye care program, made the announcement while presenting his keynote paper at an orientation on childhood blindness for journalist at the National Press Club yesterday.

Orbis International and Bangladesh Nari Sangbadik Kendra jointly organised the orientation under National Childhood Blindness Reduction Program at Orbis and the National Eye Care.

Presenting his keynote speech, Enayet said although no national survey was conduction on child blindness in the country, the World Health Organisation (WHO) estimated the number of child blindness patients using Under-5 child mortality rate.

Currently, the Under-5 child mortality rate is at 53, so it can be said that the estimated number of child blindness patients would be around 25,000, he added.

He also added: We had conducted cataract surgery of more than 10,000 children between 2005 and 2010. When we reviewed the success of these operations, we observed that many of the operation did not give satisfactory outcomes as the patient did not come for treatment at an earlier age.

He urged the people to bring their children, who are suffering from eyesight problem, for treatment and informed that the government will be providing all kinds of eye care treatment, including surgery, free of cost.

When asked, Dr Munir Ahmed, country director of Orbis International for Bangladesh, told the Dhaka Tribune: I will not disagree with him [Enayet] but before using this data it should be validated in some way.

However, the number of child blindness patients had definitely reduce in number. But, a large number of children continue to suffering from avoidable childhood illnesses.

He further said early detection of the problem, quality of treatment and post-treatment care can prevent avoidable blindness or restore the sight of the children.

Child eye experts said avoidable child blindness and visual impairment is a significant health issue in Bangladesh and its impact fuels poverty and worsens socio-economic inequality.

They also added that children of Bangladesh have been suffering of different eye related issues, such as cataract, refractive error, strabismus, rop (retinopathy of prematurity), ptosis and eye injury.

Quoting WHO, global estimates of childhood blindness show that the prevalence of childhood blindness in Bangladesh is at 0.75 per 1,000 children.

They said approximately 1.3 million children have refractive errors and around 1,53,600 have low vision problems, of which around 78,336 can be avoided.

Without intervention, blind or visually-impaired children are likely to experience low educational achievement, lack of productive employment opportunities, social isolation and increased poverty.

Among others, Mohammed Alauddin, director program of Orbis, Dr Nahid Ferdousi, co-ordinator of National Childhood Blindness Reduction Program, Dr. Lutful Husain, staff optholmologist at Orbis, and Parvin Sultana Jhuma, general secretary of Bangladesh Nari Sangbadhik Kendra, also addressed the program.

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Eye doctor explains why you shouldn’t look at the sun during the … – NorthJersey.com

August 19th, 2017 7:41 am

Experts are warning people about counterfeit eclipse glasses.

Watching solar eclipse(Photo: Daniel MacDonald / http://www.dmacphoto.com, Getty Images/Flickr RF)

You've heard over and over that you shouldn't look up at the sun during Monday's solar eclipse (or ever, as a general rule), but what actually happens if you do?

Dr. Jacob Chung, Chief of Opthalmology at Englewood Hospital and Medical Center, answered our burning (ahem) questions about what'll happenif you just can't help but take a peek sans ISO-approved glasses during the big event.

If you look at it for a second or two, nothing will happen. Five seconds, I'm not sure, but 10 seconds is probably too long and 20 seconds is definitely too long.

The eye works like a camera, and the retina is like the film of your eye. So looking at the sun too long is almost like burning a hole in the center of your film, or retina. We don't have pain fibers there so you won't have discomfort or feel pain, but you might see a fuzzed out, dark spot.

The retina can't heal itself, so the blind spot is permanent and cannot be treated, but definitely go see a doctor to make sure it's the right diagnosis.

ECLIPSE GUIDE: Everything you need to know about the solar eclipse

GLASSES: 5 places to get eclipse glasses before the big day

If you're in that 70-mile swath where you'll be able to see the total eclipse [parts of Oregon, Idaho, Wyoming, Nebraska, Montana, Illinois, Kentucky, South Carolina], you have about a two-minute window where the sun is 100 percent eclipsed. Because we have a partial eclipse, there is a zero-second window where it's safe to look at the sun directly.

Look, no one loves to look at the sun: it hurts. The reason it's more dangerous during the eclipse is because you don't feel much discomfort, yet your eyes are receiving all the harm. It's similar to getting sunburnedon a cloudy day.

[Chuckles] Yes.

They filter out a lot more of the sun's harmful radiation something like 100,000 times more than standard sunglasses.

The best alternative is to visualize it from an indirect method. Put your phone camera on selfie mode, then turn your back to the sun and see the eclipse that way.

Or, take twopieces of cardboard or paper. Cut a hole in one and again, turn yourback to the sun and hold it up against the second one. Thesun will cast its rays through the pinhole, [creating a projection on the second piece of cardboard/paper].

I had a case many years ago of a gentleman who had a condition called solar retinopathy. I don't know if it was during an eclipse, but he said he was on LSD and looked at the sun for four straight hours. In hisretina there was a pigmented spot and his vision was very poor, needless to say. Hewas basically legally blind.

In summer, of course, since we're closer to the sun. But there are different ways you can get damage from the sun in your eyes. If you are outdoors a lot you can get a growth on the surface of your eye, called pterygium. It's found very commonly in people who live or grew up in equatorial regions, and a lot of surfers get itbecause the water reflects UV into eyes [the condition is also called Surfer's Eye]. If very severe, it can start to obscure your vision and cause irritation from time to time. That can be surgically removed, however.

Chronic sun exposure can also contribute to formation of cataracts and macular degeneration. So, wear sunglasses as often as it makes sense to.

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Blood cancer: High doses of vitamin C could encourage stem cells to die – Express.co.uk

August 17th, 2017 8:48 pm

The study suggests it may encourage blood cancer stem cells to die.

Researchers say Vitamin C may "tell" faulty stem cells in the bone marrow to mature and die normally, instead of multiplying to cause blood cancers.

They explained that certain genetic changes are known to reduce the ability of an enzyme called TET2 to encourage stem cells to become mature blood cells, which eventually die, in many patients with certain kinds of leukaemia.

The new study, published online by the journal Cell. found that vitamin C activated TET2 function in mice engineered to be deficient in the enzyme.

Study corresponding author Professor Benjamin Neel, of the Perlmutter Cancer Centre in the United States, said: "We're excited by the prospect that high-dose vitamin C might become a safe treatment for blood diseases caused by TET2-deficient leukemia stem cells, most likely in combination with other targeted therapies."

He said changes in the genetic code that reduce TET2 function are found in 10 per cent of patients with acute myeloid leukaemia (AML), 30 per cent of those with a form of pre-leukaemia called myelodysplastic syndrome, and in nearly 50 per cent of patients with chronic myelomonocytic leukaemia.

Such cancers cause anaemia, infection risk, and bleeding as abnormal stem cells multiply in the bone marrow until they interfere with blood cell production, with the number of cases increasing as the population ages.

Prof Neel said the study results revolve around the relationship between TET2 and cytosine, one of the four nucleic acid "letters" that comprise the DNA code in genes.

To determine the effect of mutations that reduce TET2 function in abnormal stem cells, the researchers genetically engineered mice such that the scientists could switch the TET2 gene on or off.

Similar to the naturally occurring effects of TET2 mutations in mice or humans, using molecular biology techniques to turn off TET2 in mice caused abnormal stem cell behaviour.

Prof Neel said, remarkably, the changes were reversed when TET2 expression was restored by a genetic trick.

Previous work had shown that vitamin C could stimulate the activity of TET2 and its relatives TET1 and TET3.

Because only one of the two copies of the TET2 gene in each stem cell is usually affected in TET2-mutant blood diseases, the researchers hypothesised that high doses of vitamin C, which can only be given intravenously, might reverse the effects of TET2 deficiency by turning up the action of the remaining functional gene.

They found that vitamin C did the same thing as restoring TET2 function genetically.

By promoting DNA demethylation, high-dose vitamin C treatment induced stem cells to mature, and also suppressed the growth of leukaemia cancer stem cells from human patients implanted in mice.

Study first author Doctor Luisa Cimmino, of New York University Langone Health, said: "Interestingly, we also found that vitamin C treatment had an effect on leukaemic stem cells that resembled damage to their DNA.

"For this reason, we decided to combine vitamin C with a PARP inhibitor, a drug type known to cause cancer cell death by blocking the repair of DNA damage, and already approved for treating certain patients with ovarian cancer."

The researchers found that the combination had an enhanced effect on leukaemia stem cells, further shifting them from self-renewal back toward maturity and cell death.

Dr Cimmino said the results also suggest that vitamin C might drive leukaemic stem cells without TET2 mutations toward death, given that it turns up any TET2 activity normally in place.

Corresponding author Professor Iannis Aifantis, also of NYU Langone Health, added: "Our team is working to systematically identify genetic changes that contribute to risk for leukaemia in significant groups of patients.

"This study adds the targeting of abnormal TET2-driven DNA demethylation to our list of potential new treatment approaches."

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From death’s door to mountain top, beating cancer the Geoff Thomas way – iNews

August 17th, 2017 8:47 pm

Only 3,224 miles to go. Let me at it, says Geoff Thomas as he prepares to set off around Spain, 21 days of pure agony covering every inch of La Vuelta, each stage completed 24 hours before the peloton attacks the third and final grand tour of the season.

Thomas is a cancer survivor dedicated through his own foundation to raising cash and awareness of blood cancer, the disease that struck down the former Crystal Palace midfielder in 2003. Thomas was diagnosed with chronic myeloid leukaemia and given just three months to live. It was, he says, a dark place, yet here he is 12 years in remission and immersed in another lung busting slog to make life possible for others.

The scale of the challenge is insane, or stupid as Thomas describes it, for a bunch of amateur cyclists, one of whom is 67 years old. Having already completed the Giro dItalia and the Tour de France on the same terms this year there is no backing out now.

The initiative is after all called the Geoff Thomas Three Tours Challenge, and for better or worse he will be in the saddle on Friday alongside four equally committed travellers to attempt something only 39 professional riders have done before. The hope is to funnel more than 1m to Cure Leukaemia, the charity set up by the man he credits with saving his life Professor Charlie Craddock.

I got involved in all this through going through the illness. My only chance of survival was stem cell replacement. At my first meeting with a doctor I was given three months to live. The next day I saw Professor Craddock and he put me in intensive chemo straight away. He offered a different prognosis, saying I might have three years.

I was lucky my sister was a very good match as the donor. The treatment more or less kills you then they bring you back to life. My sister had to have the stem cells removed from her spine, quite a painful procedure. These days its like giving blood. They harvest the cells from a blood sample. As a result more people are going on the donors list.

Back when I was diagnosed there was a clinical trial that I couldnt get on. It proved very successful, resulting in survival rates of more than 90 per cent for the drug involved. There was no real infrastructure to run clinical trials back in 2003. A lot of hospitals did not have the facilities, no clinical researchers in place etc. For a small amount of money in the grand scheme we are now able to put that into place.

Hospitals are now working together to get the results required and survival rates have gone up. As a result of the work we have done with clinical trials we have seen almost 200m worth of drugs available for free to patients on the NHS. And that is something we are really proud of.

The fight goes on, and so do the fundraisers, and for this one, you can never be ready, says Thomas. Some of the climbs are ridiculous. I dont look at the course or whats head I just think of bringing enough weight to bear on the pedal to turn the wheel. And you have to be lucky.

I missed a few days of the Tour de France after I fell and injured my hip. It was only on day two, a flat bit, and it became infected about ten days later. I was gutted to have to stop but I realised my aim is to get awareness out there and pull in the money that I know is making a difference to peoples lives. This is the final leg. Im determined tol stay on the bike this time and make it to the end.

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Cisplatin Combination Kills Rare Cancer Cells in Mice – Bioscience Technology

August 17th, 2017 8:47 pm

An experimental drug combined with the traditional chemotherapy drug cisplatin, when used in mice, destroyed a rare form of salivary gland tumor and prevented a recurrence within 300 days, a University of Michigan study found.

Called adenoid cystic carcinoma, or ACC, this rare cancer affects 3,000-4,000 people annually, and typically arises in the salivary glands. It's usually diagnosed at an advanced stage, is very resistant to therapy, and there's no cure. People may have read about ACC in the news lately, because elite professional runner Gabe Grunewald is currently undergoing her fourth round of treatment since her 2009 ACC diagnosis.

Typically, oncologists treat ACC tumors with surgery and radiation. They rarely use chemotherapy because ACC is extremely slow-growing, and chemotherapy works best on cancers where cells divide rapidly and tumors grow quickly, said Jacques Nr, a U-M professor of dentistry, otolaryngology and biomedical engineering, and principal investigator on the study.

The Nr lab treated ACC tumors with a novel drug called MI-773, and then combined MI-773 with traditional chemotherapy cisplatin. MI-773 prevents a molecular interaction that causes tumor cells to thrive by disarming the critical cancer fighting protein, p53.

Study co-author Shaomeng Wang, U-M professor of medicine, pharmacology and medicinal chemistry, discovered MI-773, which is currently licensed to Sanofi.

Researchers believe that blocking that interaction sensitized ACC cancer cells to cisplatina drug that under normal conditions, wouldn't work. When administered to the mice with ACC tumors, the cisplatin targeted and killed the bulk cells that form the tumor mass, while MI-773 killed the more resistant cancer stem cells that cause tumor recurrence and metastasis.

"This drug MI-773 prevents that interaction, so p53 can induce cell death," Nr said. "In this study, when researchers activated p53 in mice with salivary gland cancer, the cancer stem cells died."

The key is that in many other types of cancer, p53 is mutated so it can't kill cancer cells, and this mutation renders the MI-773 largely ineffective. However, in most ACC tumors p53 is normal, and Nr said researchers believe this makes these tumors good candidates for this combined therapy.

Researchers performed two different types of experiments to test ACC tumor reduction and recurrence. First, they treated tumors in mice with a combination of MI-773 and cisplatin, and tumors shrank from about the size of an acorn to nearly zero.

In the second experiment, the acorn-sized tumors were surgically removed, and for one month the mice were treated with MI-773 only, with the hope of eliminating the cancer stem cells that fuel recurrence and metastasis.

"We did not observe any recurrence in the mice that were treated with this drug after 300 days (about half of mouse life expectancy), and we observed about 62 percent recurrence in the control group that had only the surgery," Nr said. "It's our belief that by combining conventional chemotherapy with MI-773, a drug that kills more cancer stem cells, we can have a more effective surgery or ablation."

One limitation of the study is that it's known that about half of all ACC tumors recur only after about 10 years, and this observational period was only 300 days.

In a typical metastasis, the cancer cells spread through the blood to other parts of the body. But ACC cancer cells like to move by "crawling" along nerves, and it's common for ACC tumor cells to follow the prominent facial nerves to the brainpicture a mountain climber ascending a ropewhere it's often fatal.

Research is still too early-stage to know how humans will respond, and the drug will work primarily in tumors where p53 is normal. If p53 is mutated, which is fairly common in other tumor types, this drug won't work as well, Nr said.

The work was funded by the Adenoid Cystic Carcinoma Research Foundation, U-M and the National Institutes of Health.

The study, "Therapeutic Inhibition of the MDM2-p53 interaction prevents recurrence of adenoid cystic carcinomas," appeared earlier this year in the journal Clinical Cancer Research.

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FDA OKs Pfizer drug for rare, fast-killing type of leukemia – ABC News

August 17th, 2017 8:47 pm

The Food and Drug Administration has approved a new medicine for use against a rare, rapidly progressing blood cancer after other treatments have failed.

The agency approved Pfizer Inc.'s Besponsa for patients with a type of advanced acute lymphoblastic leukemia. By then, life expectancy is low.

"These patients have few treatments available and today's approval provides a new, targeted treatment option," Dr. Richard Pazdur, the FDA's director for cancer drugs, said in a statement.

This year an estimated 5,970 Americans will be diagnosed and 1,440 will die from the cancer, according to the National Cancer Institute.

The drug will cost $168,300 without insurance for the typical nine-week treatment course.

In testing that included 218 patients, 36 percent given Besponsa had their cancer vanish for eight months on average; 17 percent of those given chemotherapy had complete remission for a median five months.

Besponsa is believed to work by blocking the growth of cancerous cells by binding to their surface.

The powerful injected drug, known chemically as inotuzumab ozogamicin, comes with the FDA's most-stringent warning because it can cause severe liver disease, including blocking veins in the liver. It also carries an increased risk of death in patients who have received a certain type of stem cell transplant.

Besponsa also can cause a decrease in blood-cell and platelet production, infusion-related reactions and problems with the heart's electrical pulses. Women who are pregnant or breastfeeding should not take Besponsa because it may harm a developing fetus or a newborn baby, the FDA warned.

More-common side effects include fatigue, severe bleeding, fever, nausea and headaches.

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Traffic fumes ‘increase infection risk by damaging immune system’ – Birmingham Mail

August 17th, 2017 8:47 pm

Air pollution could increase the risk of infection by damaging the immune system, according to a study.

Scientists have demonstrated for the first time that nano-sized particles in traffic fumes reduce the body's ability to kill viruses and bacteria.

While the potential link between car-choked streets and illness has been the subject of much debate, the work at Edinburgh Napier University is the first to show this effect and presents significant human health implications.

Dr Peter Barlow, who led the research, said: "This is an area of research that is very poorly understood.

"We were extremely concerned when we found that air pollution particles could inhibit the activity of these molecules, which are absolutely essential in the fight against infection.

"In light of these findings, we urge that strong action plans are put in place to rapidly reduce particulate air pollution in our towns and cities."

The study focused on tiny molecules found in the immune systems of humans and animals, known as antimicrobial peptides, which increase in response to infection.

It found carbon particles could trigger changes in the molecules, potentially resulting in "an increased susceptibility to infection".

The implications are potentially profound for people living in areas of high air pollution, who breathe in huge concentrations of particles every day or absorb them through skin contact.

Those with pre-existing lung conditions like asthma or chronic obstructive pulmonary disease are said to be especially vulnerable.

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Scripps Research Institute Awarded $11.2M for Mammalian Immune System Project – Times of San Diego

August 17th, 2017 8:47 pm

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The Scripps Research Institute announced Thursday that it was awarded a five-year, $11.2 million federal grant to continue a long- running project to reveal the detailed workings of the mammalian immune system.

The project, which also includes professors from the Center for Infectious Disease Research in Seattle, Stanford University and the University of Texas Southwestern, aims to map the molecular and cellular interactions that underlie immunity and inflammation in health and disease. That in turn should enable the invention of better drugs and vaccines for infections, inflammatory diseases, and other immune-related ailments, according to TSRI.

The project has been funded by the National Institute for Allergic and Infectious Diseases, part of the National Institutes of Health, for 15 years.

It is one of the most productive large-scale science grants that NIAID funds, said Richard Ulevitch professor in TSRIs Department of Immunology.

The researchers use a system called forward genetics, in which the scientists create random DNA mutations in a population of test animals.

They screen the animals for resulting immune-related changes and, when they find significant ones, use state-of-the-art DNA sequencing technology to identify the mutated genes that caused the modifications.

The researchers also mine existing literature on gene and protein function, and apply the statistical and computational methods of systems biology, to connect the data points and thereby map the networks that underlie immunity.

Over the years, the scientists have published noteworthy findings in scientific journals and maintained online databases with their results.

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A pathology atlas of the human cancer transcriptome – Science Magazine

August 17th, 2017 8:47 pm

Mathias Uhlen

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.Center for Biosustainability, Danish Technical University, Copenhagen, Denmark.School of Biotechnology, AlbaNova University Center, KTHRoyal Institute of Technology, Stockholm, Sweden.

Cheng Zhang

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Sunjae Lee

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Evelina Sjstedt

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Linn Fagerberg

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Gholamreza Bidkhori

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Rui Benfeitas

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Muhammad Arif

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Zhengtao Liu

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Fredrik Edfors

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Kemal Sanli

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Kalle von Feilitzen

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Per Oksvold

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Emma Lundberg

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Sophia Hober

School of Biotechnology, AlbaNova University Center, KTHRoyal Institute of Technology, Stockholm, Sweden.

Peter Nilsson

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Johanna Mattsson

Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Jochen M. Schwenk

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.

Hans Brunnstrm

Division of Pathology, Lund University, Skne University Hospital, Lund, Sweden.

Bengt Glimelius

Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Tobias Sjblom

Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Per-Henrik Edqvist

Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Dijana Djureinovic

Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Patrick Micke

Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Cecilia Lindskog

Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Adil Mardinoglu

Science for Life Laboratory, KTHRoyal Institute of Technology, Stockholm, Sweden.School of Biotechnology, AlbaNova University Center, KTHRoyal Institute of Technology, Stockholm, Sweden.Department of Biology and Biological Engineering, Chalmers University of Technology, SE-412 96 Gothenburg, Sweden.

Fredrik Ponten

Department of Immunology Genetics and Pathology, Uppsala University, Uppsala, Sweden.

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Blood Biopsy Reveals Unique, Targetable Genetic Alterations in Patients with Rare Cancer – UC San Diego Health

August 17th, 2017 8:47 pm

Using fragments of circulating tumor DNA in blood, University of California San Diego School of Medicine researchers were able to identify theoretically targetable genetic alterations in 66 percent of patients with cancer of unknown primary (CUP), a rare disease with seven to 12 cases per 100,000 people each year.

In order to plan treatment for cancer in general, physicians first attempt to pinpoint the primary cancer where the tumor first developed. In CUP, despite its spread throughout the body, the origin remains unknown, making treatment more difficult. The current standard of care is platinum-based combination chemotherapies with a median survival time of six to eight months.

Razelle Kurzrock, MD, director of the Center for Personalized Cancer Therapy at Moores Cancer Center at UC San Diego Health.

In a study published in the journal Cancer Research on August 15, researchers report that by sequencing circulating tumor DNA (ctDNA) derived from blood samples in 442 patients with CUP, they were able to identify at least one genetic alteration linked to cancer in 290 66 percent of patients. Researchers used a screening test developed by Guardant Health that evaluates up to 70 genes. Based on known carcinogenic mutations, 99.7 percent of the 290 patients who had detectable tumor DNA in their bloodstream had genomic alterations that could hypothetically be targeted using existing FDA-approved drugs (as off-label use) or with therapies currently under investigation in clinical trials.

By definition, CUP does not have a definite anatomical diagnosis, but we believe genomics is the diagnosis, said Razelle Kurzrock, MD, director of the Center for Personalized Cancer Therapy at Moores Cancer Center at UC San Diego Health and senior author. Cancer is not simple and CUP makes finding the right therapy even more difficult. There are multiple genes and abnormalities involved in different areas of the body. Our research is the first to show that evaluating circulating tumor DNA from a tube of blood is possible in patients with CUP and that most patients harbor unique and targetable alterations.

A blood or liquid biopsy is a diagnostic tool based on the idea that critical genetic information about the state of disease can be found in blood or other fluids. One vial of blood could be used to detect the onset of disease, monitor its progression and measure its retreat less invasively than a tissue biopsy.

Shumei Kato, MD, assistant professor of medicine at UC San Diego School of Medicine.

Another advantage of the liquid biopsy is that the location of the cancer does not matter, said Shumei Kato, MD, assistant professor of medicine at UC San Diego School of Medicine and first author. With a blood sample, we can analyze the DNA of tumors throughout the body to find targetable alterations. With tissue biopsies, we can only see genomic changes that are in that one site and that may not be the same as what is in different sites not biopsied, such as the lung or bone.

Liquid biopsies are relatively simple to get and can be obtained regularly to monitor changes over time, as was the case with a 60-year-old woman with CUP. Her case, which was evaluated by Brian Leyland-Jones, MB, BS, PhD and study co-author with colleagues at Avera Cancer Institute, was described in the study to show the changes observed in ctDNA over the course of her treatment.

What we saw was that the patient was responding to treatment, but the cancer had emerging new mutations, said Kurzrock. Whats new here is that we can do the same evaluation through a blood test that we previously could only do with a tissue sample. You will see these changes with a simple blood test and it is easy to repeat blood tests, but hard to repeat tissue biopsies.

The study also reported the case of an 82-year-old man who was prescribed a checkpoint inhibitor immunotherapy as part of his treatment because of a mismatch repair gene anomaly that is typically observed in less than two percent of patients. He showed a partial response within eight weeks and blood biopsies showed the tumor DNA disappearing.

We can see that each patient has different mutations in their tumor DNA, which means that treatment plans cannot be a one-size-fits-all approach; a personalized approach is needed, said Kato.

Kurzrock is already using liquid biopsy technology in the Profile Related Evidence Determining Individualized Cancer Therapy (PREDICT) clinical trial a project focusing on the outcome of patients who have genomic testing performed on their tumors and are treated with targeted therapy.

The authors suggest that a liquid biopsy approach should be further investigated in next-generation clinical trials focusing on CUP.

Co-authors include: Nithya Krishnamurthy, Scott M. Lippman, UC San Diego; Kimberly C. Banks, Richard B. Lanman, Guardant Health, Inc.; Pradip De, Kirstin Williams, and Casey Williams, Avera Cancer Institute.

This research was funded, in part, by the National Cancer Institute (P30 CA016672) and the Joan and Irwin Jacobs fund.

Disclosure: Razelle Kurzrock receives consultant fees from X-biotech and from Actuate Therapeutics, as well as research funds from Genentech, Pfizer, Sequenom, Guardant, Foundation Medicine and Merck Serono, and has an ownership interest in Novena Inc. and CureMatch Inc.

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On the trail of yellow fever – Science Magazine

August 17th, 2017 8:44 pm

Monkeys and mosquitoes hold clues to when and where the virus could resurge in Brazil.

Researchers Bruna Sena Nascimento (foreground) and Hlio Saraiva climb a tree to capture mosquitoes in the canopy in Santa Barbara, Brazil.

The howler monkeys slink like cats through the canopy, swiveling their heads to look for danger. They have reason to be wary. In the jungle below, biologists armed with a black tranquilizer rifle are hunting them, flashes of khaki through the foliage.

The scientists signal each other with snaps and whistles and pivot directions frequently; they often cross trails perpendicularly instead of following them. As they maneuver for clean shots, thick leaves come rattling down through the branches. In the distance, marmosets whistle.

The scientists are on Ilha Grande, an island off southern Brazil that once housed a notorious maximum security prison. Resorts dot the perimeter today, but untouched jungle dominates the interior. Brazil recently experienced its worst outbreak of yellow fever in decades with hundreds of cases, some just east of Ilha Grande. So scientists plan to test local howler monkeys (called bugios) for the virus to learn whether it has spread here, too. If they can catch one.

Suddenly, a shota sharp hiss. A 20-centimeter dart with a red tuft for a tail rockets upward. The shooter is Filipe Abreu, a Ph.D. student at the Oswaldo Cruz Foundation (Fiocruz), a research institute in Rio de Janeiro, Brazil. Abreu looks as if he's been in the wild for weeks: muddy pants, scruffy beard, machete dangling from his belt. He's an entomologist, but the intricate transmission cycle of yellow fever, which involves both monkeys and mosquitoes, compels him to study primates, too.

The shot misses. Instead of leaves, the dart comes clattering down. A second shot also goes awry, striking a branch and bending the needle tip 45.

The party regroups, and Abreu hands the rifle to Marcelo Quintela Gomes, a technician at Fiocruz. The hunters thread through vines and shinny down trees into a gully. Every so often Gomes raises the rifle, then drops it. He eventually takes three shots, all misses. Everyone agrees that the bugios are unusually skittish.

They're not the only ones. Yellow fever has left the people of Brazil feeling edgy as well. Over the past 8 months, they've endured vaccine shortages, lurid media stories, and the occasional slaughter of innocent monkeys. To stem such problems, scientists have scoured this massive country to figure out where the virus lurks and how it's spreadingknowledge vital to fighting future outbreaks as well. But fear remains, especially the fear that yellow fever will ravage the megacities along Brazil's east coastor push even beyond that.

We've seen Zika march up to the United States, says Seth Berkley, CEO of Gavi, the Vaccine Alliance, in Geneva, Switzerland. So have dengue fever, chikungunya, and other mosquito-borne diseases. There's no reason to think yellow fever won't do the same, he says.

YELLOW FEVER WAS ONCE the world's most feared disease. Most victims suffer only fevers and aching joints, but 15% get walloped: Their eyes and skin turn yellow, and they bleed from the mouth and eyes. (The Spanish name for the disease, vomito negro, means black vomit.) No drugs exist to treat it, and half of those who develop the serious form die as the virus destroys their livers.

Native to Africa, yellow fever spread to the Americas with the slave trade. In 1793, then-President George Washington fled Philadelphia, Pennsylvania (then the U.S. capital), during an epidemic that killed 5000. Later outbreaks nearly derailed the construction of the Panama Canal.

A vaccine developed in the 1930s largely eliminated the disease in North America. Africa and South America, meanwhile, continue to suffer. Sub-Saharan Africa accounts for 90% of cases, including a 2016 outbreak centered in Angola with thousands of victims. But in some ways yellow fever in South America is scarier: Because of the low natural immunity there, it kills one-third of those who contract it.

Brazil seems particularly vulnerable. Yellow fever long ago disappeared into the interior, and given the mere handful of cases most years (2014 saw none at all), few people outside endemic areas get vaccines. But in December 2016, victims began appearing in the east for the first time since 1942. The government confirmed 792 cases in 130 cities nationwide, with several hundred more under investigation. More than half occurred in Minas Gerais (population: 21 million), a southeastern state bordering the states of Rio de Janeiro (17 million) and So Paulo (44 million). One victim reportedly died within 40 kilometers of the city of Rio.

State health ministries, which administer vaccines, have ordered 26.3 million emergency doses since December, but some places still ran short. During Carnival in February, a squirrel monkey died of yellow fever in Utinga State Park in Belm in northern Brazil. After panicked stories in the press, people stampeded vaccine clinics, which had to open extra rooms to contain the crowds. After 12,000 inoculations in 5 days, Belm's clinics exhausted their supply.

Although the onset of winter slowed the outbreak, scientists fear a resurgence next year. When and where it might reappear depends on the erratic and often maddening behavior of three animals: mosquitoes, monkeys, and humans.

TWO TRANSMISSION CYCLES of yellow fever exist in South America. In the sylvatic (jungle) cycle, mosquitoes from two generaSabethes and Haemagogusspread the virus mostly between monkeys, with people (usually loggers or miners in remote areas) bitten and infected only incidentally. But the possibility of an urban cycle looms. Here, a different mosquito, the infamous Aedes aegypti, spreads the disease directly from person to person, and cases quickly multiply. All the recent cases in Brazil have been sylvatica slight misnomer because some have occurred inside citiesbut no human-to-human transmission has occurred.

Bruna Sena Nascimento brings the mosquitoes she catches in the forest (top) back to a lab at the Evandro Chagas Institute in Belm, Brazil (bottom), where she identifies the species and checks for signs of the yellow fever virus.

Pinning down which mosquito species carry the virus can yield clues about who is at risk and where. So on a recent June morning, entomologists from the Evandro Chagas Institute in Belm don green jumpsuits and drive north to the jungle. On the way, they swap stories about all the mosquito-borne diseases they've endured. Leathery old Hlio Saraiva has had three strains of dengue.

They park at a dilapidated banana farm and start gathering equipment. Just in case, bring the big knife, someone says. Saraiva grabs a 45-centimeter machete with ENTOMOLOGIA on the scabbard. As they head off, the farm's resident Dalmatian trots up to join the adventure.

After several turns, they stop. Twelve meters above is a platformor rather, four ragged planks. Yellow fever mosquitoes dine on monkeys in the canopy, so researchers have to scale trees, too. There's no ladder, just a few dozen nails pounded into the trunk to hoist yourself up. It's a drenching climb in the heat.

An ignorant reporter asks what they use for mosquito bait. Bruna Sena Nascimento, an animated entomologist, laughs. We are the bait. Oh. Mosquitoes are attracted to the carbon dioxide that primates exhale. So unlike with monkeys, hunting mosquitoes is easy: Just sit and waitand hold off on the bug spray.

In the old days, researchers sometimes sat on platforms in their underwear, counting bites and noting what parts of the body mosquitoes preferred. Now, fully clothed scientists use short white nets to nab mosquitoes in the air. They then slip tubes into the nets, suck the bugs up with their lungs, and puff them out into collection vesselsanything from sawed-off sections of PVC pipe to plastic Teenage Mutant Ninja Turtles cups with lids. (Entomology is a cheap science, Abreu says. You improvise.) A half-day in the canopy can net a few hundred skeeters.

Back at the lab in Belm, Nascimento freezes and sorts her mosquitoes, focusing on the abdominal stripes or sweeping back legs that distinguish various species. After the sorting, the mosquitoes go into vials filled with saline and a BB. An automatic agitator then liquefies the bugs, producing a foamy gray ink with floating legs. The fluid is added to cell cultures to test for yellow fever.

Although scientists know the disease's main vectors in Brazil, they're still investigating whether others play a role. One mystery is how outbreaks shift from sylvatic to urban and what species drive that shift. Perhaps miners or loggers simply carry the virus back to cities. But certain mosquitoes might play a role, too. Abreu suspects that A. albopictus, the Asian tiger mosquito, which often straddles jungle and urban areas, might harbor the virus and could bridge the cycles by introducing cases into new areas.

Even the known vectors wreak plenty of havoc, though. Says Thomas Monath, a yellow fever expert at NewLink Genetics, a biotech company in Ames, Iowa: In Brazil, they've drawn a line that supposedly demarcates risk. We vaccinate people on one side and don't vaccinate people living on the other side. But mosquitoes aren't observing that demarcation.

IF MOSQUITOES ARE THE VILLAINS of yellow fever, monkeys are the main victims. A lack of natural immunity leads to devastating outbreaks for many South American species, especially howler monkeys. In the throes of the disease, Abreu says, they often descend from trees to riverbanks to slake their thirst, but lack the strength to climb up again. They end up shivering in the dirt, wracked with pain.

During the Brazilian outbreak, health officials nationwide asked people to report sightings of sick or dead monkeys so they could test for yellow fever. They received reports of 5300 dead monkeys since the outbreak started, with an unknown number related to yellow fever. Biologists also carried out active vigilance campaigns, such as the hunts on Ilha Grande.

Shooting monkeys on those hunts is only half the challenge. After the tranquilizer hits, scientists have about 5 minutes before the monkey passes out and plummetsduring which time they're scrambling about with a net, hoping like crazy it doesn't wander into some inaccessible area. Once it lands safely, they check its gums, eyes, and genitals for yellow discoloration, then take blood from the groin to test for virus. Although the monkey usually wakes within an hour, it might remain loopy for several more, rendering it vulnerable to falling or a jaguar attack. So scientists usually detain itone group uses a red dog carrieruntil it recovers its wits.

Most people in Brazil know that monkeys can catch yellow fever. Alas, many also believe that monkeys infect people, which isn't true. (Mosquitoes do.) As a result, people in rural areas sometimes shoot monkeys or leave poisoned fruit around, adding dozens of casualties to an already devastating outbreak. Killing monkeys ends up harming humans as well, says Jlio Bicca-Marques, a primatologist at the Pontifical Catholic University of Rio Grande do Sul in Porto Alegre, Brazil: The death of monkeys from yellow fever is the first warning that the virus is circulating. In other words, monkeys are sentinels, he says, early detection systems. Without the monkeys in our forests, we'll be blind.

HUMAN BEINGS, the third actor in this drama, are the least predictable. Miners and loggers, some with fake immunization cards, jet between sylvatic regions and cities in just hours, potentially transferring the virus to new areas. Cutting down forests also exposes people to mosquitoes that would otherwise remain hidden.

Building homes in forest clearings, a common practice in Brazil, is especially risky. On one side of the road might sit shanties with chickens wandering about and satellite dishes anchored onto mossy boulders. On the other, a wall of thick jungle with vibrant red tropical birds and playful monkeys. Jozelene Beckmann, who lives in Belm, home of the state park where the squirrel monkey died, says that monkeys used to cavort along her rooftop and slip inside her home. Unfortunately, where monkeys go, mosquitoes followas does yellow fever. After years of ignoring recommendations, Beckmann finally got vaccinated in mid-June.

Briefly anesthetized, a monkey has its blood drawn to check for yellow fever virus.

Vaccinating infants for yellow fever is already mandatory in northern and Amazonian states, where the disease is endemic, and some scientists propose extending the law nationwide. But because vaccination carries a small riskone in 300,000 people develops full-blown yellow fever after vaccination and another one in 100,000 develops meningitisthe government has stopped short of mandating it for everyone, instead merely recommending it. Many people in Rio and other cities ignore the recommendation. One problem is that most vaccine clinics keep short hours, and with the Brazilian economy struggling, people can't take time off work to visit.

The low compliance frustrates scientists because inoculation could basically eliminate yellow fever nationwide, and do so at a pittance. A single dose given as an infant that costs a dollar is effective for life. That's extraordinary, Monath says. During the Angolan emergency last year, health officials stretched vaccine supplies with fractional doses of one-fifth the normal amount, and even that seemed to offer short-term protection.

Still, making the vaccine has its challenges. It's hard to scale up production, for one thing, partly because many steps are still performed by hand, the same basic way they were in the 1930s. Manufacturers grow the virus in chicken eggs, which workers must candle one by one with hand lamps to check for signs of live embryosveins, eyes, movement. (Dead eggs are discarded.) A single technician might examine 8000 eggs per week. Technicians also must burn holes in the eggshells with torches to introduce the virus, and later burn more holes around the waist of the egg to extract the infected embryos for grinding in blenders. It's not quite artisanal vaccine production, but it's close.

Another problem is more perverse: The vaccine is almost too good at preventing yellow fever. Because it costs so little and protects people for life, making it isn't profitable. Worldwide, just four institutes bother, including Fiocruz. Manufacturers also dislike the uneven market for it: low demand most years, followed by outbreaks that leave them scrambling. Production at Fiocruz, for instance, jumped from 25 million doses in 2016 to a planned 70 million this yearwhich forced the institute to cut back severely on its vaccine for measles, mumps, and rubella.

The market could soon change, however. The World Health Organization (WHO) recently brokered deals in several African and South American countries to vaccinate 584 million people for yellow fever over the next decade, with a goal of eliminating all outbreaks worldwide by 2026. That campaign should steady the market by ensuring stable demand. To boost supply, Fiocruz is also building a new $1 billion plant west of Rio that, in a few years, could produce up to 100 million doses of yellow fever vaccine annually.

Still, WHO notes that production of vaccine almost always lags behind projections. Lack of urgency among political leaders could also weaken the campaign. Public health authorities, says Monath, can basically forget about [the disease] in between these horrible episodes. So although the new Fiocruz facility will help, eliminating outbreaks worldwide remains an ambitious goal. The quick spread of Zika and other mosquito-borne diseases from South America up to Texas and Florida also suggests that yellow fever will be hard to tame.

During the yellow fever outbreak this year, public health clinics in Belm, Brazil, vaccinated hundreds of people daily.

But the danger of yellow fever in North America pales in comparison with the disaster that could arise if it ever spread to Asia. Even though southern Asia has all the prerequisites for yellow fevermonkeys, mosquitoes, a warm climatethe disease has never gained a foothold on the world's most populous continent. Perhaps, some scientists speculate, other diseases there provide cross-immunity. Or perhaps humans have simply been lucky. But last year, 11 Chinese men working in Angola developed yellow fever upon returning home, the first confirmed cases in Asian history. Thankfully, the disease spread no further. But if the urban cycle ever got established there, 1.8 billion peoplevirtually all unvaccinated and presumably with high genetic susceptibilitycould be vulnerable.

Moreover, the struggle to contain yellow fever, a familiar disease with an effective vaccine, does not augur well for our ability to combat the new diseases that will almost certainly emerge as people push deeper into jungles. As Jon Abramson, a pediatrician at Wake Forest University in Winston-Salem, North Carolina, and a yellow fever adviser for WHO, puts it: If we can't stop outbreaks with yellow fever, we're in a lot of trouble with other outbreaks.

IN BRAZIL, the quest to stop the current outbreak continues. On Ilha Grande, after the howler monkeys scatter, the hunting party takes a break to catch insects. Sometimes we get mosquitoes and can't get monkeys; other times, we get monkeys but can't get mosquitoes, Abreu says philosophically. Both are important.

But after tracking those two creatures all morning, Abreu and Gomes now switch their attention to the final animal in the yellow fever triad: humans. To that end, they visit the abandoned prison nearby, now a museum.

Locals there are gossiping about a tourist who recently found a dead monkey nearby and posted a picture on Facebook. Unfortunately, something dragged the carcass off before authorities could test it for yellow fever.

Abreu befriends the museum guard, whose backyard is a popular crossing point for monkeys. She's quite taken with the tranquilizer rifle, and he shows her how it works. Afterward they exchange contact information, so she can alert him if she sees sick or dead monkeys. She then asks Abreu whether it's true that monkeys give yellow fever to humans. He assures her that they don't.

Late the next morning, Gomes finally bags a bugio, a female. Instead of tumbling from the canopy, she slides down a thick shaft of bamboo like that pole the firemen come down, Abreu says. But she is unharmed, and they get a good blood sample.

A few weeks later, the results come back: negative for yellow fever. That's a reliefno sign yet that this ancient scourge has infiltrated the island paradise. But with nearby mainland cities confirming cases and tourists pouring in, it might not be long. As the rest of Brazil has shown, exemption from yellow fever today is no guarantee of a safe tomorrow.

Link:
On the trail of yellow fever - Science Magazine

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