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Gene therapy: What personalized medicine means for you – Stock Daily Dish

December 15th, 2019 7:44 am

Thuy Truong thought her aching back was just a pulled muscle from working out. But then came a high fever that wouldnt go away during a visit to Vietnam. When a friend insisted Truong, 30, go to an emergency room, doctors told her the last thing she expected to hear: She had lung cancer. Back in Los Angeles, Truong learned the cancer was at stage 4 and she had about eight months to live.

My whole world was flipped upside down, says Truong, who had been splitting her time between the San Francisco Bay Area and Asia for a new project after selling her startup. Ive been a successful entrepreneur, but Im not married. I dont have kids yet. [The diagnosis] was devastating.

Doctors at the University of Southern California took a blood sample for genetic testing. The liquid biopsy was able to detect tumor cells in her blood, sparing her the risky procedure of collecting cells in her lungs.

Genetic sequencing allowed the lab to isolate the mutation that caused her cancer to produce too much of the EGFR (epidermal growth factor receptor) protein, triggering cancer cells to grow and proliferate. Fortunately, her type of mutation responds to EGFR-targeting drugs, such as Tarceva or Iressa, slowing tumor growth.

Unlike chemotherapy, which blasts all fast-growing cells in its wake,go after specific molecules. That makes them more effective at fighting particular types of cancers, including breast, colorectal and lung cancers. Now the approach is being expanded to fight an even broader range of cancers. Its all part of a new wave in health care called .

This is the future of medicine, says Dr. Massimo Cristofanilli, associate director for translational research and precision medicine at Northwestern University. There is no turning back. The technology is available and there are already so many targeted therapies.

Most medical treatments have been designed for the average patient, leading to a one-size-fits-all approach. But with vast amounts of data at their disposal, researchers now can analyze, our family histories and other health conditions to better understand which types of treatments work best for which segments of the population.

This is a big deal. But it requires the know-how of geneticists, biologists, experts inand computer scientists who understand big-data analytics. Several startups have already begun this work.

, founded by researchers at the University of Toronto, uses AI to predict how genetic mutations will change our cells and the impact those changes will have on the human body., co-founded by scientists and physicians from Stanford University, is building a map of what turns our genes on and off, giving physicians a guide they could use to craft personalized therapies. And, a small San Francisco startup, provides personalized advice on nutrition and wellness based on your DNA.

Just like Facebook learns to automatically recognize Aunt Martha in your family photos, Deep Genomics finds and categorizes patterns in genetic data. Once its found those patterns, the companys deep learning system can infer if and how changes to your DNA affect your body.

Thats a big step forward compared with current genetic tests. Most can only give a probability of, say, getting breast cancer based on data from an entire population. Other tests cant even tell you if the genetic changes theyve detected mean anything.

The work is personal for Brendan Frey, CEO and co-founder of Deep Genomics and a professor at the University of Toronto. Fourteen years ago, he and his wife discovered their unborn baby had a genetic condition.

We knew there was a genetic problem, but our counselor couldnt tell us if it was serious or if it was going to turn out to be nothing, Frey says. We were plunged into this very difficult, emotional situation.

The experience made Frey want to bridge the divide between identifying and understanding what they mean.

Deep learning or machine learning when computers teach themselves as they see more data can also help doctors know which drugs will most effectively treat a patients illness and whether that person is more likely to experience side effects.

It can also help predict how cancer cells will mutate. And that can help drug companies come up with new treatments as tumor cells change and patients no longer respond to the drugs that worked.

That could help turn a disease like cancer into a manageable chronic ailment, says Cristofanilli.

Where Deep Genomics analyzes patterns in genetic data to predict when mutations will make you sick, Epinomics looks at epigenomics, or the study of what turns our genes on and off.

The company describes it like this: If your genome, which shows what genes we have, is the hardware of our bodies, then the epigenome is its software programming. Epinomics aims to decode that programming.

Every cell in the body carries the same genetic code. But cells in the heart, brain, bone and skin function differently based on this programming. It happens because chemical markers attach to DNA to activate or silence genes. These markers, known as the epigenome, vary from one cell type to another and are affected by both nature (inheritance) and nurture, which can include the air we breathe and the food we eat.

Researchers think a disruption to the epigenome can cause illnesses such as,or. Understanding it could give physicians a guide to the best options for each patient, like having a GPS for treatments at the molecular level.

We are focusing on what is happening at the programming level of each cell, says Epinomics co-founder Fergus Chan. Once we understand how genes are being turned on and off, well be able to better predict which treatments will work or whether changes to lifestyle will have an impact on health.

When Vitagene co-founder and CEO Mehdi Maghsoodnia asked a doctor what vitamins he should be taking, he was handed a bottle of pills and told to hope for the best.

That was the beginning of Vitagene, which uses genetic data and other health information culled from a detailed questionnaire to deliver a personalized nutritional supplement plan that lists which vitamins you need and in what doses, as well as what to avoid.

Maghsoodnia offers an alternative to the one-size-fits-all $27 billion US dietary supplement industry. Customers pay $99 to have their DNA tested and blood analyzed. And for $69 a month, Vitagene will package and ship supplements in dosages tailored to your individual needs.

The Food and Drug Administration estimates there are more than 85,000 dietary supplements on the US market, most of which are unregulated. Nearly all are promising everything from anti-aging to weight loss, and no science behind it to tell you what works for you, says Maghsoodnia. We help filter through the noise.

Vitagenes algorithm has been tested on patients whove had bariatric surgery for weight loss, which often leaves them deprived of key nutrients. Vitagene helped develop a supplement regimen to get these patients the nutrition they need after surgery.

Precision medicine is in its early days.

This is especially true for psychiatry and its exploration of how the brain responds to the environment, stress and genetic disorders. Now several companies are selling tests to help psychiatrists select drug treatments by looking at patients DNA mutations and their metabolizing rate.

But critics caution that these genetic tests may be overselling their capabilities.

Precision medicine has been very promising in oncology, says Jose de Leon, a professor of psychiatry at the University of Kentucky who specializes in psychopharmacology. But we know a lot more about cancer and how it works. In psychiatry, its much harder because we dont know enough about how the brain works.

Yes, precision medicine holds enormous promise.

Even so, Northwesterns Cristofanilli cautions clinicians to stay grounded in reality. It can be difficult to understand where reality becomes imagination, he says. We want to make sure we are protecting patients from claims that we may not deliver.

For her part, Truong is grateful to benefit from the work thats already been done. Im an engineer, she says.

I dont believe in miracles. I believe in science.

This story appears in the spring 2017 edition of CNET Magazine. For other magazine stories, click.

: The CNET team reminds us why tech stuff is cool.

: In Europe, millions of refugees are still searching for a safe place to settle. Tech should be part of the solution. But is it? CNET investigates.

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Seasons readings to end this year or start the next with – Albuquerque Journal

December 15th, 2019 7:44 am

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ALBUQUERQUE, N.M. Decisions, decisions. What books to get as holiday gifts for family and friends?

Here are some suggested books published this year to help narrow your choices.

n New Mexicos Palace of the Governors: Highlights from the Collections edited by Daniel Kosharek and Alicia Romero. (Museum of New Mexico Press). From front to back, this book is source of enjoyment, admiration and enlightenment, containing materials of wildly diverse subjects and many periods in the museums collections. For example, theres the image on the front cover, and on page 157, of five men of the Santa Fe Fire Department bearing intense expressions and wearing smart deep red coats, dark pants and stylish hats. The photo, an ambrotype, was taken between 1861 and 1880, and helps the reader understand the collecting function of the Palace of the Governors in Santa Fe. Ambrotype and tintype, the book states, are cased image processes that followed the ground-breaking daguerreotype. The book is a companion to the exhibit A Past Rediscovered set to open March 6, 2020 at the New Mexico History Museum in Santa Fe. A Race Around the World: The True Story of Nellie Bly & Elizabeth Bisland written by Caroline Starr Rose, illustrated by Alexandra Bye. (Albert Whitman & Company). On Nov. 14, 1889, the two ladies in the title both New York journalists began their competition in a global race against each other and against time. Nellie headed east by steamer. Elizabeth westward by train. Nellie eventually won the race. But there was more at stake. The participants were making a statement about womens independence. As Rose, an Albuquerque resident, writes in conclusion, Both journeyed alone. Both took on the world and triumphed, each on her own terms. Byes illustrations are bright, attractive and draw the reader to the art and the text. The audience is ages 4-8. Our History is the Future: Standing Rock versus the Dakota Access Pipeline, and the Long Tradition of Indigenous Resistance by Nick Estes. (Verso). From his indigenous perspective, the author details how a small 2016 Indian protest of the planned Dakota Access oil pipeline blossomed into the largest indigenous protest movement of this century. Estes also thinks of the anti-pipeline movement as a statement of goals growing out of the tradition within the long history of native resistance in the United States. The context relates in part to the contentious white-indigenous relations stretching back into the 19th century.

Estes is a citizen of the Lower Brule Sioux tribe and an assistant professor of American Studies at the University of New Mexico.

Noel Street by Richard Paul Evans. (Gallery) Evans, the author of The Christmas Box and other seasonal bestsellers, is out with a new novel, Noel Street. Set in 1975, the novel is about love, faith, family and forgiveness. Elle is a single mom working as a waitress at the Noel Street Diner in Mistletoe, Utah. She meets William, a recently returned Vietnam POW suffering from war-related mental demons. In spite of his own issues, he may hold the key to unlock Elles secret pain. This is the third book in Evans Noel Christmas collection. The Rabbit Effect: Live Longer, Happier, Healthier with the Groundbreaking Science of Kindness by Dr. Kelli Harding. (Atria) Research in 1978 was the starting point for the authors reportage of investigations into the value of hidden, crucial factors in understanding health, factors such as love, friendship and community.

Theres a social dimension to health weve completely overlooked in our scramble to find the best and most cutting-edge personalized medical care, Dr. Harding writes in the introduction. She isnt the first person to probe medicines connection to kindness or compassion. But her book contributes to a greater understanding of the link. Harding is an assistant clinical professor of psychiatry at Columbia University Irving Medical Center.

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Personalized Medicine Market Outlook, Growth by Top Company, Region, Application, Driver, Trends and Forecasts By 2026| Verified Market Research -…

December 15th, 2019 7:44 am

New Jersey, United States: The report titled Personalized Medicine Market is one of the most comprehensive and important additions to Verified Market Researchs archive of market research studies. It offers detailed research and analysis of key aspects of the Personalized Medicine market. The market analysts authoring this report have provided in-depth information on leading growth drivers, restraints, challenges, trends, and opportunities to offer a complete analysis of the Personalized Medicine market. Market participants can use the analysis on market dynamics to plan effective growth strategies and prepare for future challenges beforehand. Each trend of the Personalized Medicine market is carefully analyzed and researched about by the market analysts.

Global Personalized Medicine Market was valued at USD 96.97 Billion in 2018 and is expected to witness a growth of 10.67% from 2019-2026 and reach USD 217.90 Billion by 2026.

The report includes detailed analysis of the vendor landscape and thorough company profiling of leading players of the Personalized Medicine market. The researchers have considered almost all important parameters for company profiling, including market share, recent development, gross margin, future development plans, product portfolio, production, and revenue.

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The report offers a comprehensive study of product type and application segments of the Personalized Medicine market. The segmental analysis provided in the report is based on significant factors such as market share, market size, consumption, production, and growth rate of the market segments studied.Readers of the report are also provided with exhaustive geographical analysis to provide clear understanding of the regional growth of the Personalized Medicine market. Developed as well as developing regional markets for Personalized Medicine have been deeply studied to help market players identify profit-making opportunities in different regions and countries.

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Analysis on Strategies of Leading Players:Market players can use this analysis to gain competitive advantage over their competitors in the Personalized Medicine market.

Regional Growth Analysis:All major regions and countries have been covered in the report. The regional analysis will help market players to tap into unexplored regional markets, prepare specific strategies for target regions, and compare the growth of all regional markets.

Segmental Analysis:The report provides accurate and reliable forecasts of the market share of important segments of the Personalized Medicine market. Market participants can use this analysis to make strategic investments in key growth pockets of the Personalized Medicine market.

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Advanced analytical research solutions within one platform; Verified Market Research. Offering information enriched research studies that include primary and secondary research studies. Verified Market Research assists in understanding holistic industrial factors and trends.

Analysts with high expertise in data gathering and governance utilize industry techniques to collate and examine data at all stages. Our analysts are trained to combine modern data collection techniques, superior research methodology, subject expertise and years of collective experience to produce informative and accurate research reports.

Verified market research partners with clients to provide insight into strategic and growth analytics; data that help achieve business goals and targets. Our core values include trust, integrity, and authenticity for our clients.

Our research studies help our clients to make superior data-driven decisions, capitalize on future opportunities, optimize efficiency and keeping them competitive by working as their partner to deliver the right information without compromise.

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Mr. Edwyne FernandesCall: +1 (650) 781 4080Email:[emailprotected]

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Healthy Aging Workshop Launches UC Partnership with Nanyang Technological University, Singapore – UCLA Samueli School of Engineering Newsroom

December 15th, 2019 7:44 am

A two-day workshop on healthy aging hosted by UCLA is kicking off a five-year partnership between the University of California system and Nanyang Technological University, Singapore.

The workshop is being held at Mong Auditorium in Engineering VI from Dec. 9-10 with several experts from NTU and the majority of UC campuses participating.

The first day focuses on technologies for healthy aging and includes talks on the role of brain-computer interfaces in brain health and on molecular mechanisms of aging and precision medicine. The neurobiology of aging and the impact of lifestyle, prevention and policy is the topic for the second day of the workshop.

UCLA Samueli participants include Jacob Rosen, a professor of mechanical and aerospace engineering, who is presenting on technology for rewiring the brain for stroke patients, and Sam Emaminejad, an assistant professor in electrical and computer engineering, whose main focus is wearable sensors and personalized medicine.

The joint effort between the two organizations fosters an exchange of faculty and students and expands academic and research opportunities in areas including health, technology, innovation and climate change.

NTU President Professor Subra Suresh and UC President Janet Napolitano signed the memorandum of understanding on behalf of their respective institutions earlier this year in February, and the health workshop is one of the initial outcomes of the partnership.

The workshop is organized by a team led by Hal Monbouquette, a UCLA Samueli professor of chemical and biomolecular engineering; NTU Graduate College Associate Dean Sierin Lim; and NTU Graduate College Dean K. Jimmy Hsia.

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Study Shows Only 40 Percent of Patients with Metastatic Colon Cancer Receive Guideline-Recommended Biomarker Testing – GlobeNewswire

December 15th, 2019 7:44 am

REDWOOD CITY, Calif., Dec. 11, 2019 (GLOBE NEWSWIRE) -- Despite longstanding medical guidelines recommending biomarker testing for all patients with metastatic colon cancer, a new study published in JCO Precision Oncology shows that only 40 percent of patients are tested according to guidelines.1 These findings are consistent with the rates seen in late-stage lung cancer, where clinical adoption of genomic profiling remains below the recommended standard-of-care guidelines.2 The result is that many patients are potentially being treated with less effective drugs, some having serious side-effects; while others are not being offered highly effective personalized treatment options.

The multi-center retrospective study also found that certain subgroups of patients were less likely to be tested than others. Suboptimal genotyping occurred more often if the patient was male, older than 65, progressed from early stage disease, or treated in a community cancer center. Furthermore, only 28 percent of patients on anti-EGFR treatments received the necessary testing to determine eligibility. This study also showed that using a comprehensive panel, as opposed to single-gene testing, could possibly result in a 50 percent increase in guideline-recommended testing rates.

For over a decade, medical guidelines have recommended multigene mutation testing for metastatic colon and rectal cancer patients to ensure patients receive the optimal treatment available. While the study shows that testing has improved slightly, the disappointing reality is that the majority of patients, including those receiving targeted treatments, are not being comprehensively tested, said Stuart Goldberg, MD, a lead study investigator who served as chief scientific officer at COTA, Inc. during the project. Personalized medicine holds great promise for achieving better outcomes, but we will not see the benefits until genomic testing is routinely adopted into clinical practice.

Newly available therapies routinely help some people with metastatic colorectal cancer gain a year or two of life, but these novel treatments cannot be applied unless comprehensive genotyping is routinely performed, said Richard Lanman, MD, Guardant Health Global Chief Medical Officer. Just as concerning was that 28 percent of patients received targeted treatments without being tested, and for some we would have known in advance that the treatment was not going to work. At Guardant we are committed to helping reverse this trend by helping to educate oncologists and offering a non-invasive and comprehensive genomic testing solution that overcomes the limitations of tissue biopsies with our Guardant360 blood test.

The American Society of Clinical Oncology (ASCO) and National Comprehensive Cancer Network (NCCN) guidelines recommend biomarker testing for all patients with metastatic colon cancer to screen for genomic alterations in KRAS, NRAS, BRAF, ERBB2 (HER2), NTRK and microsatellite instability (MSI) to help guide more effective treatment decisions. Targeted therapies and immunotherapies have been shown to improve clinical outcomes. For example, anti-EGFR therapies are commonly used in treating metastatic colon cancer but are not efficacious in patients whose tumors harbor KRAS, NRAS, or BRAF V600E mutations.3 Additionally, immunotherapy is effective in patients with MSI and anti-HER2 treatment is effective in patients with ERBB2 (HER2) amplifications.4,5 Professional guidelines continue to be updated as new therapies come to market such as the recent recommendation to test patients for NTRK fusions because they may benefit from treatment with tumor-agnostic NTRK inhibitors.

Study details can be found here.

About Guardant HealthGuardant Health is a leading precision oncology company focused on helping conquer cancer globally through use of its proprietary blood tests, vast data sets and advanced analytics. The Guardant Health Oncology Platform leverages capabilities to drive commercial adoption, improve patient clinical outcomes and lower healthcare costs across all stages of the cancer care continuum. Guardant Health has launched liquid biopsy-based Guardant360 and GuardantOMNI tests for advanced stage cancer patients and LUNAR assay for research use and for use in prospective clinical trials. In parallel, Guardant Health is actively exploring the performance of the LUNAR assay in initial studies related to screening and early detection in asymptomatic individuals.

Forward Looking StatementsThis press release contains forward-looking statements within the meaning of federal securities laws, including statements regarding the adoption of Guardant Healths products, which involve risks and uncertainties that could cause Guardant Healths actual results to differ materially from the anticipated results and expectations expressed in these forward-looking statements. These statements are based on current expectations, forecasts and assumptions, and actual outcomes and results could differ materially from these statements due to a number of factors. These and additional risks and uncertainties that could affect Guardant Healths financial and operating results and cause actual results to differ materially from those indicated by the forward-looking statements made in this press release include those discussed under the caption Risk Factors in Guardant Healths Annual Report on Form 10-K for the year ended December 31, 2018, and in its other reports filed by Guardant Health with the Securities and Exchange Commission. The forward-looking statements in this press release are based on information available to Guardant Health as of the date hereof, and Guardant Health disclaims any obligation to update any forward-looking statements provided to reflect any change in its expectations or any change in events, conditions, or circumstances on which any such statement is based, except as required by law. These forward-looking statements should not be relied upon as representing Guardant Healths views as of any date subsequent to the date of this press release.

In light of the foregoing, investors are urged not to rely on any forward-looking statement in reaching any conclusion or making any investment decision about any securities of Guardant Health.

Investor Contact:Lynn Lewis or Carrie Mendivilinvestors@guardanthealth.com

Media Contact:Anna Czene or Ian Stonepress@guardanthealth.com

References1. Gutierrez ME, Price KS, Lanman RB, et al. Genomic Profiling for KRAS, NRAS, BRAF, Microsatellite Instability (MSI) and Mismatch Repair Deficiency (dMMR) among Patients with Metastatic Colon Cancer. JCO Precision Oncol. December 20192. Leighl NB, Page RD, Raymond VM, et al. Clinical Utility of Comprehensive Cell-Free DNA Analysis to Identify Genomic Biomarkers in Patients with Newly Diagnosed Metastatic Non-Small Cell Lung Cancer. Clin Cancer Res. April 20193. Van Cutsem E, Khne CH, Lng I, et al. Cetuximab plus irinotecan, fluorouracil, and leucovorin as first-line treatment for metastatic colorectal cancer: updated analysis of overall survival according to tumor KRAS and BRAF mutation status. J Clin Oncol. May 20114. Overman MJ, Lonardi S, Wong KYM, et al. Durable clinical benefit with nivolumab plus ipilimumab in DNA mismatch repair-deficient/microsatellite instability-high metastatic colorectal cancer. J Clin Oncol. March 20185. Sartore-Bianchi A, Trusolino L, Martino C, et al. Dual-targeted therapy with trastuzumab and lapatinib in treatment-refractory, KRAS codon 12/13 wild-type, HER2-positive metastatic colorectal cancer (HERACLES): a proof-of-concept, multicentre, open-label, phase 2 trial. Lancet Oncol. April 2016

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Triple-Negative Breast Cancer Now Has a Targeted Agent – Cancer Therapy Advisor

December 15th, 2019 7:44 am

On March 8, 2019, the US Food and Drug Administration (FDA) approved the PD-L1 inhibitor atezolizumab for first-line treatment of metastatic triple-negative breast cancer in combination with nab-paclitaxel chemotherapy for patients who are ineligible for surgery and whose tumors express PD-L1. This marks the first time a regimen approved for breast cancer includes an immunomodulator, and represents the first targeted agent approval in triple-negative breast cancer a disease that, historically, has only had chemotherapy as a treatment option.

Triple-negative breast cancer is an especially aggressive subtype of breast cancer that is identified by the absence of expression of estrogen, progesterone, or HER2 protein receptors on the cancers surface. These proteins, when present in other subsets of breast cancer, allow us to target and take advantage of the protein to kill the cancer cell. For patients with triple-negative metastatic cancer, the average survival is only slightly more than a year, meaning that half of women diagnosed with this disease will not live beyond that benchmark.

This groundbreaking approval was based on results of the IMpassion130 trial (ClinicalTrials.gov Identifier: NCT02425891), for which Sarah Cannon, the Cancer Institute of HCA Healthcare in Nashville, Tennessee, participated. The IMpassion130 trial treated 902 women with either nab-paclitaxel alone or nab-paclitaxel in combination with atezolizumab.

A post-hoc update of long-term progression-free survival revealed that in the PD-L1 immune cell-positive population, the updated median progression-free survival was 7.5 months

(95% CI, 6.79.2) with atezolizumab plus nab-paclitaxel and 5.3 months (95% CI, 3.85.6) for nab-paclitaxel alone (stratified hazard ratio [HR], 0.63; 95% CI, 0.500.80; P <.0001).1

In patients with PD-L1positive tumours, median overall survival was 25 months (95% CI, 19.630.7) with atezolizumab and 18 months (13.620.1) with placebo. The stratified hazard ratio for overall survival was 0.71 (95% CI, 0.540.94).1

Immunotherapy treatments help a patients immune system recognize cancer as foreign and attack it. In contrast to chemotherapy, which can be thought of as poison for cancer cells, immunotherapy is essentially a way to boost ones own immune cells to fight cancer. Chemotherapy has known side effects, such as hair loss, nausea, and fatigue; however, the side-effect profile for immunotherapy treatment is different. Patients receiving immunotherapy treatment may experience low thyroid hormone levels or inflammation in the lungs or gastrointestinal system. When treating patients with immunotherapy, it is important to closely monitor patients for these rare side effects and treat them with steroids when appropriate.

The approval of atezolizumab not only represents a win for some patients with triple-negative breast cancer characterized by PD-L1 expression, it also more broadly represents a win for personalized medicine. In the past decade, we have gotten smarter about knowing that every persons cancer may be driven by individual mutations and alterations. We have had access to tests to examine the expression of estrogen receptors, progesterone receptors, and HER2 receptors for some time, but only now do we know to test for PD-L1, which allows us break this broad disease down into smaller subsets using the markers the cancer possesses, and, prescribe more targeted treatments. We have also started looking at a broader profile of the alterations in a cancer through molecular profiling, where hundreds of genes are examined for mistakes and abnormal copy numbers in an attempt to personalize care. Tailoring treatment to each person and their individual cancer characteristics at the cell level will become even more common in the coming years.

IMpassion130 also highlights the benefit of clinical trials not just for future patients, but also for those who are currently enrolled. I treated patients enrolled in this trial, and in fact, we still have patients who are receiving this therapy years after their diagnosis. This trial and this agent highlight the advances we make in cancer treatment every day through the power of clinical trials. Unfortunately, only about 2% to 5% of adults with cancer participate in clinical trials in the US and more than 50% say they are not even aware of the existence of trials.2,3 These studies show us that we need to continue to work toward making clinical trials a well-understood concept through patient education, dispelling misconceptions, and celebrating the big advances, such as the approval ofatezolizumab in this patient group.

Erika Hamilton, MD, is the Director of the Breast Cancer and Gynecologic Cancer Research Program at Sarah Cannon Research Institute in Nashville, Tennessee.

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How is Radiomics the Next Wave in Medtech? – Medical Tech Outlook

December 15th, 2019 7:44 am

FREMONT, CA: Diagnostics and treatment have undergone sea changes in recent years. The field which was dominated by traditional medical technologies is now on the cusp of artificial intelligence-driven changes. The area of radiology has also come under the influence of advancement, leading to the emergence of radiomics. The development has been helping the medical industry in dealing with the imminent shortage of qualified radiologists. Innovators have put their brains together and taken diagnostic scanning to the next level with radiomics. Radiomics is still in a developmental phase, but it has already contributed to the healthcare industry. Some ways in which the technology is helping medical fraternity is mentioned in the list below.

Immunohistochemical Evaluations

Patients can be checked for immunohistochemical (IHC) characteristics with the help of radiomics-based imaging. Medical researchers have successfully created unique machine learning models that can detect thyroid nodules in patients with high degrees of accuracy. The development makes the process non-invasive and enables the prediction of hormonal presence in patients. Computer topography imaging techniques cannot present ICH related information. According to experts, these capabilities make a timely diagnosis of thyroid cancers possible and feasible.

Brain Tumor Detection and Treatment

Current technologies for detection and classification of malignant brain tumors are good enough, but with radiomics, the amounts of data that can be extracted increases substantially. Subsequently, radiomic analysis can generate insightful data which are helpful for diagnosis, evaluation, and treatments. The advanced imaging also enables practitioners to adhere to recently announced protocols which vary significantly from the standard ones. One of the significant advantages of using radiomics in brain tumor assessment is that it allows the determination of molecular characteristics which help categorize molecular subtypes.

Diagnosis of Cancers in Breast, Lungs and Neck

Radiomics has been widely adopted by medical fraternity for the neck, lungs, and breast cancer diagnosis, treatment, and prognosis. Predicting the stage of cancer in cancer-afflicted patients with minimum or no invasive procedures is a significant step forward. Radiomics has shown excellent results in projecting the differences which help in classifying the stage of cancer. Even reoccurrence predictions have been benefitted with radiomic signature-based investigations. The ability of radiomics to take into consideration a higher number of factors and features by combining recorded clinical information makes it useful in early detection of breast, lungs, and neck cancers. In the case of breast cancer patients, radiomics is predicting response to therapy with high accuracy and thus optimizing treatment.

Precision Medicine

High sensitivity and high specificity are the remarkable features of radiomics. As the medical industry adopts precision medicine, radiomics is all set to play a very crucial role. Radiomics is powerful because it applies artificial intelligence and deep learning characteristics to radiology, thus helping define tissues with much more accuracy. Every patient can undergo a radiomics-based diagnosis and come up with personalized reports. These reports can relay detailed information which enables doctors to prescribe personalized medication or treatment models. Thus, radiomics is helping extract qualitative and quantitative data which make precision medicine possible.

Reading and interpreting medical data is challenging. However, radiomics is transforming decision-making by bettering identification and characterization. One can expect the diagnosis to become faster and error-free as computerization becomes central to the process. Subsequently, patient care will also improve as doctors gain access to deeper health insights.

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Global Precision Medicine Market Key Insights And Growth Scenario Coverage of Top Key Players 2019-2026 – Market Research Sheets

December 15th, 2019 7:44 am

GMI Research has recently published a report on Global Precision Medicine market, the report highlights the key ongoing market trend, market growth, drivers and restraints of Global Precision Medicine market. The report provides the forecast data for the period of 2019 to 2026. GMI Research analysts have a thorough understanding of the market as they are on top of any market trends and developments, which help them to understand current market dynamics, market competitive landscape and future trends of Global Precision Medicine in a couple of years.According to the report, the Global Precision Medicine Market is projected to grow at a CAGR growth of ~XX% through the forecast period from 2019 to 2026 owing to various key factors such as Precision medicine is being eyed upon as lucrative business investment opportunity by the major pharmaceutical companies owing to the rising patient preference for personalized treatment, advancements in wireless technologies and big data analytics, and tremendous increase in genetic diseases such as cancer. Our analyst knows the importance of data and are also aware of the significance of providing accurate data. The analyst deploys various approaches from primary research to credible secondary research sources and validates the data from multiple sources to make sure that our client gets the accurate picture of the Global Precision Medicine and the market size, market projections, competitive landscape etc.The reports also profile the major market players. The major players are Illumina, Inc., GE Healthcare, Roche Group, bioMerieux SA, IBM Corporation, Novartis AG, and Abbott Laboratories among others.Request Sample Report Now at Link https://www.gmiresearch.com/report/global-precision-medicine-market/sample-requestKey areas the report on Global Precision Medicine market addresses are: What are the major market drivers influence the growth of Global Precision Medicine? Which region provides the maximum growth opportunities? What makes one product more attractive over another and ranking of all the products and the market opportunity they provide? What are the key developments and how they are impacting the Global Precision Medicine market? What are the current key trends of Global Precision Medicine? How the competitive landscape looks like and what strategies companies are adopting to increase their market share?How the insights on Global Precision Medicine will help our clients in critical decision making? Help our client to know all the segments and sub-segments in detail Assessment of competitive landscape of Global Precision Medicine Details of new product launch trend, innovations, market expansions and other strategies adopted by major players Regional market trends and opportunities available in each region North America, Europe, Asia Pacific and RoWSpeak to Research Analyst to Understand more About Research at Link https://www.gmiresearch.com/report/global-precision-medicine-market/Competitive Landscape key players main strategies and their product offerings Major players products strength on each segment and vertical Product Benchmarking analysis of key players Key Players Recent Developments and strategic directionRequest for Customization at Link https://www.gmiresearch.com/report/global-precision-medicine-market/request-for-customizationAbout GMI ResearchGMI Research provides research and consulting solutions to our clients. We help our global clients through independent fact-based insights, ensuring their business achieve success by beating the competition. We provide syndicated research, customized market and competitive intelligence research, sales enablement support and data analytics services.Contact UsGMI ResearchLevel 1, The Chase Carmanhall Road, Sandyford Industrial Estate,Dublin D18 Y3X2, IrelandPh. No: +353 1 442 8820Email: [emailprotected]Web: https://www.gmiresearch.com

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Aspen Neuroscience gets funding to pursue personalized cell therapy for Parkinsons disease – The San Diego Union-Tribune

December 15th, 2019 7:44 am

Aspen Neuroscience, a new San Diego biotech company working on stem cell treatment for Parkinsons disease, has come out of stealth mode and raised $6.5 million to pursue clinical testing for its therapy.

Co-founded by well-known stem cell scientist Jeanne Loring, Aspen Neuroscience proposes creating stem cells from modified skin cells of Parkinsons patents via genetic engineering.

The stem cells, which can become any type of cell in the body, then would undergo a process that makes them specialize into dopamine-releasing neurons.

People with Parkinsons lose a large number up to 50 percent at diagnosis of specific brain cells that make the chemical dopamine.

Without dopamine, nerve cells cannot communicate with muscles and people are left with debilitating motor problems.

Once these modified skin cells have been engineered to specialize in producing dopamine, they can be transplanted into the Parkinsons patient to restore the types of neurons lost to the disease.

The reason we called it Aspen is because l was raised in the Rocky Mountain states, said Loring. When there is a forest fire in the Rockies, the evergreens are wiped out but the aspens are the fist that regenerate after the burn. So it is a metaphor for regeneration.

Aspen still has a long way to go before its proposed therapy would be available to Parkinsons patients. It has been meeting with the U.S. Food and Drug Administration to provide animal trial data and other information in hopes of getting permission to start human clinical trials.

But the company expects the earliest it would get the go-ahead from FDA to start human trials would be 2021.

Loring has been working on the therapy for eight years. She is professor emeritus and founding director of the Center for Regenerative Medicine at the Scripps Research Institute.

Loring co-founded the 20-employee company with Andres Bratt-Leal, a former post-doctoral researcher in Lorings lab at Scripps.

Joining them as Aspens Chief Executive is Dr. Howard Federoff, former vice chancellor for health affairs and chief executive of the University of California Irvine Health System.

Federoff said the company is the only one pursuing the use of Parkinsons patients own cells as part of neuron replacement therapy.

Aspens proprietary approach does not require the use of immuno-suppression drugs, which can be given when transplanted cells come from another person and perhaps limit the effectiveness of the treatment.

Aspens approach is a therapy that is likely to benefit from the fact that your own cells know how to make the best connections with their own target cells in the brain, even in the setting of Parkinsons disease, said Federoff. So when transplanted it is able to set back the clock on Parkinsons.

In addition to Aspens main therapy, it is researching a gene-editing treatment for forms of Parkinsons common in certain families.

Aspens research work up to now has been supported by Summit for Stem Cell, a non-profit on which provides a variety of services for people with Parkinsons disease.

The new seed funding round was led by Domain Associates and Axon Ventures, with additional participation from Alexandria Venture Investments, Arch Venture Partners, OrbiMed and Section 32.

Aspens financial backing, combined with its experienced and proven leadership team, positions it well for future success, said Kim Kamdar, a partner at Domain Associates. Domain prides itself on investing in companies that can translate scientific research into innovative medicines and therapies that make a difference in peoples lives. We clearly see Aspen as fitting into that category, as it is the only company using a patients own cells for replacement therapy in Parkinsons disease.

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ViewRay teams with Elekta and Medtronic on MR-guided radiation therapy – DOTmed HealthCare Business News

December 15th, 2019 7:44 am

ViewRay has inked respective agreements with Elekta AB and Medtronic that aim to increase understanding into and practices of MR-guided radiation therapy.

The partnerships will each include the establishment of clinical studies to assess the impact and benefits provided by the treatment, as well as probes into additional therapeutic areas in which the technology could prove beneficial.

"We are pleased to announce these important collaborations and investments in ViewRay, said ViewRays president and CEO Scott Drake in a statement. Our goal is to concurrently prove the value of MR-guided radiation therapy and strengthen our balance sheet.

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Elekta will also invest in ViewRay, taking on a minority interest with the potential to rise to 9.9 percent.

Elekta believes that competition is crucial to drive the adoption of any new technology, and that is why we are committed to continuing to develop and offer customers our high-field Elekta Unity and promoting this technology to benefit patients worldwide, said Elekta's president and CEO Richard Hausmann in a statement. By investing in ViewRay, we ensure that the two inventors of MR-guided radiation therapy continue to drive the paradigm shift forward.

The deal between Medtronic and ViewRay is a similar clinical collaboration, that will make use of the MRIdian MR-guided radiation therapy system in studies. Medtronic has also committed to investing in a minority share of ViewRay as part of the deal.

"We are well-positioned to drive MRIdian to standard of care, noted Drake, adding that, the ability to see clearly during the procedure, track tumors and soft tissues, and auto-gate the beam is integral to delivering highly precise, personalized medicine."

The agreements with Elekta and Medtronic follow a rough period for ViewRay, which was,hit with an investor lawsuit in September, filed over allegedly false or misleading statements made regarding negative operational and financial issues reported in August.

Specific allegations included failure to disclose that demand for ViewRay systems dropped due, in part, to changes around Medicare reimbursement; overstating reported backlog; and damages suffered by investors because of materially false and misleading statements made by ViewRay at all relevant times. Upon disclosing these challenges, the companys stock price fell by more than 50 percent. It also slashed its previously issued full fiscal year 2019 financial guidance.

In addition to the deals with Elekta and Medtronic, ViewRay's biggest shareholder, Fosun International Limited will be putting in more money in order to keep its ownership percentage at present levels.

The investments from Elekta and Medtronic, however, will only take place if at least $75 million is raised. Elekta's investment will also require an aggregate cap of $36 million.

The deals are non-binding, subject to various terms and conditions.

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AI Is Central To The Longevity Financial Industry – Forbes

December 15th, 2019 7:43 am

150 financial institutions advancing the Longevity financial industry

There are over 1 billion people currently in retirement. New types of financial institutions are evolving to satisfy the needs of this aging population. Investment banks, pension funds, and insurance companies are developing new business models, and are using AI to improve the quality of the analytics used to formulate them. In the near future, the synergy between innovative AI and wealth management will lead to the creation of a new financial institutions optimized for the aging population. Age-friendly Longevity banks will make banking services easier and safer for seniors.

Over 150 financial companies are already developing innovative WealthTech and AgeTech products and services and AI is central to the process. AI drives Longevity, Longevity enables AgeTech, AgeTech enables WealthTech, and WealthTech supports interest in Longevity as an industry. This makes the ongoing growth of AgeTech and WealthTech inevitable.Many innovative financial institutions are in development such as Longevity-focused venture funds, Longevity-AgeTech banks, Longevity index funds and hedge funds, and even a specialized stock exchange for Longevity-focused companies and financial products.

The 7th Continent - 1 billion people in retirement globally.

AgeTech

AgeTech refers to technologies and services optimized for people over 60. AgeTech services enable older people to conduct banking with less difficulty and also helps protect them from financial fraud. AgeTech products for seniors include tablets, smartphones, computers, banking interfaces, medical alert systems, and phone amplifiers. AgeTech is not limited to the financial industry. For instance, theres a growing demand for smart homes for older people. Age friendly smart homes provide AI products and services that make it possible for people to stay in their own homes even if they require special care. The AgeTech segments potential is forecasted to reach $2.7 trillion by 2025, showing 21% annual market growth.

WealthTech

WealthTech companies produce products and services that simplify and enhance the creation and maintenance of wealth. WealthTech companies, which offer advice based on AI and big data, are adapting existing products and services to enhance the financial situation of people over 60. These companies are implementing innovations to address the financial challenges that many seniors face. The following are four examples of WealthTech.

Top 150 pension funds, banks, insurance companies, reinsurance companies, and asset management firms ... [+] advancing Longevity, AgeTech, WealthTech

Longevity Stock Exchange

There are hundreds of Longevity startups in the UK, EU, US and Asia and 99% of them are not publicly traded. This means that they are limited to seeking funding from angel investors and venture investors, which represents a very small fraction of available global wealth. This situation creates an extreme funding deficit and a major illiquidity problem.Almost all DeepTech sectors are facing this situation, but the negative repercussions are particularly bad for the Longevity industry, as it leads to reduced quality of life and unnecessary suffering for many older people. It also threatens to inflict crippling economic effects on national healthcare systems, pensions, social security systems, and national economies. Furthermore, in many cases investors exploit the gross illiquidity for their own financial advantage, to the detriment of Longevity and DeepTech startups.

In the future a Longevity Stock Exchange will be developed to deal with specialized derivatives. This will be a means by which investors can provide increased liquidity to the Longevity industry, and will lead to a self-sustaining cycle of growth in the Financial Longevity Industry whereby the effect of aging on GDP is repeatedly offset and the wealth created is reinvested into technologically reinvigorated human capital. The increased liquidity will enable greater flexibility and growth for companies listed on the exchange, and will help advance the Longevity industry as a whole. Setting up a Longevity Stock Exchange will require the public listing of at least 100 Longevity focused companies to create enough diversity and potential volume for trading.

Novel Financial Institutions for the Longevity Economy

AgeTech Longevity Banks

The growth of the aging population will be accompanied by a proliferation of other products including new types of savings accounts, specialized retirement plans, and specialized financial advising. As a consequence, new types of financial products, new asset classes, new investment strategies, and longer-dated bonds and securities will be developed. Traditional banks, as opposed to challenger banks, are taking the first steps in AgeTech and adapting their infrastructure for people over 60. For example, HSBC has partnered with the Alzheimers Society to create dementia-friendly products, and Barclays is actively developing software for seniors to make their customer experience more comfortable.

Over the next few years, it is likely that WealthTech and AgeTech will come to be regarded as complementary functions and AgeTech Longevity Banks reconfigured specially for seniors will emerge. Rising life expectancy is creating new opportunities for the financial sector and as the proportion of people in retirement continues to grow, an increasing number of products and services will be offered. New financial institutions optimized for people 60+ will help transform the growing aging population from a global threat into a global opportunity and will spawn a whole new industry the capitalization of which could exceed anything ever conceived of by financial markets.

Click here to preview a new book that I co-authored with my colleague Dmitry Kaminskiy Longevity Industry 1.0 - Defining the Biggest and Most Complex Industry in Human History.

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No More Snake Oil: Science Has Finally Uncovered Legitimate Ways to Boost Our Life Span – Robb Report

December 15th, 2019 7:43 am

According to a popular quip, age is down to mind over matter: If you dont mind, then it doesnt matter. But enough people do mind that the anti-aging industry is worth some $100 billionand countingevery year.

Sadly for those people, and the rest of us, attempts to halt the clock seem as futile now as when our ancestors searched for the Fountain of Youth. The modern but ghastly practice of so-called vampire infusions of young bloodcosting $8,000 a literbecame the latest age-defeating bunk consigned to the trash, following a warning last year from the Food and Drug Administration that they dont work.

No great surprise therenor that people were willing to try it. As I move through my 40s, conventional anti-aging advice from scientists and doctors has remained much the same: Eat your greens, exercise, dont drink and get plenty of sleep. Thanks for nothing. Cant science in 2020 do better?

Courtesy of Unsplash

Actually it can. After centuries of snake oil and false promises, work on anti-aging is moving from untested quackery to the lab.

For starters, scientists now have a more accurate way to measure aging than simply counting birthdays. Its called an epigenetic clock. In exchange for $300 and a small vial of my blood,a company called myDNAge measured mine last year. I did this out of both professional and personal curiosityand because I was secretly convinced that beneath my middle-aged exterior lies a much younger man, and I wanted science to confirm that.

Developed by Steve Horvath of UCLA, the test analyzed more than 2,000 locations on my DNAfor signs of biochemical changes called methylation. These changes, the addition of tiny chemical tags, accumulate over time, depending on our lifestyles, and affect how genes work. Ive never smoked, dont drink as much as I used to and no longer receive birthday cards from local takeout restaurants, so I thought my DNA would be in good shape.

I was wrong. In a short and unemotional report, the company told me that sample BL745677 showed my DNA age was 48: 12 months older than my calendar age. It got worse. Of all the other 47-year-olds who took the test, some two-thirds of them have younger genes than I do. Id like to say my first reaction was shock and humility. Instead I assumed the test was wrong. And then I read Horvaths take on that: Its really more likely that planet Earth will be hit by an asteroid tomorrow than that this predictor doesnt work. Ive never heard a scientist talk like that, with no comforting caveats to soften the blow (or counteract lawsuits and peer objections) and no margin for error offered to console my bruised vanity.

Courtesy of Unsplash

Still, what can be measured can be managed, and epigenetic clocks could finally offer a robust way for science to extend our life spans. It gives us a chance to see what worksand the motivation to use it. I got my results in June, and spurred into action, Ive started to run again. Ive lost 10 pounds and now drink alcohol only on weekends. Next year I plan to get my DNA age checked again, and I hope to have lost that extra year and then some.

If that sounds too much like hard work, youll be pleased to learn that shortcuts are being developed. Several anti-aging scientists have told me they take a common diabetes drug called metformin. And test results published last year suggest why: Metformin can help wind back the epigenetic clock. Blood tests taken before and after showed that the subjectsall men in their 50s and 60s who took the drugs for 12 months in a small trialshed an average of 2.5 years.

Scientists arent sure yet how metformin does this, but bigger trials exploring epigenetic clocks are planned to confirm its so. Only then would it be widely available. At the moment, however, many committed users must buy the drug online. Thats not for me: Its impossible to know for sure what youre getting. Countering the earlier motto, I do mind about my age, but it doesnt matter so much that Id take that risk. Its unlikely that either exercise or metformin will take me to 120 years, but that we can measure progress at alland shave a few years off our agetells me future interventions should indeed get us to an extended, healthy life span. Until then, Ill continue to run against the clock.

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Serena Williams Reveals Secret To Longevity, Gives Venus Williams Advice – International Business Times

December 15th, 2019 7:43 am

KEY POINTS

Serena Williams revealed how she managed to keep her winning ways and gave her sister Venus a piece of advice.

In her stellar career, Williams has ultimately become one of the greatest tennis players of all time. However, the five-time WTA Tour winner doesnt really believe she is womens Tennis GOAT.

In a recent interview with Tennis World USA, Williams said that she never thought that her name will be included in GOAT talks. In fact, even to this day, Williams doesnt think about it too much.

When my career started I never thought that I would be even in the conversation of the greatest. Now I don't think of a number too much. Obviously I would like if get to a certain number, but I don't think about it too much because I don't want to be. I just want to enjoy every moment that I have, Williams said.

Williams then revealed her simple secret to longevity. According to legendary tennis player, she doesnt put the pressure of winning more Grand Slams on herself and just want to enjoy every moment.

You know, every time I win Grand Slams, if I continue and I will try my best to win more I just want to have fun with it, so... I think what enables me to win more is the fact that I don't put that pressure on myself, Williams revealed.

The Olympic gold medalist also spoke about her sister Venus, who, despite dealing with Sjogren syndrome, has kept competing at the highest level.

According to Serena, if she werein Venus shoes, she would have opted to play doubles.

If I were Venus, I probably would have been like, Well, I might just play doubles, Serena said.

But Serena admires her sisters eagerness to still compete despite the fact that Venus might never be the same player she once was.

But her spirit and her, like, it's just amazing because I know what she goes through more than anyone else here, and sometimes she's doing great and sometimes it's different and it's difficult. She might lose matches that she would normally win 10 times out of 10, but to accept that and keep going is really amazing, Serena of her sister Venus.

Serena Williams hugs Venus Williams after her loss to her sister during Day 8 of BNP Paribas Open on March 12, 2018, in Indian Wells, California. Photo: Kevork Djansezian/Getty Images

Just recently, Serena posted a touching message about Venus on social media. Serena wrote the caption next to an Instagram photo of Venus standing on a beach showering the older Williams some sisterly love.

Doubles partner sister soulmate one of my fav sisters@venuswilliams, Serena wrote.

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Learn the importance of having an income distribution plan – Press of Atlantic City

December 15th, 2019 7:43 am

By now, most people know they should have a financial plan, even though many do not. But what about an income distribution plan? For decades, the benefits of financial plans have been discussed but only for the last few years have we begun to hear about income plans. The reason for the recent discussion is due to our aging population. According to a 2017 AARP study, 10,000 baby boomers are turning 65 every day, and this is expected to continue into the 2030s!

Investors have been taught well how to save and invest for their retirements, but they havent had nearly enough education on how to spend what they have taken most of their lives to accumulate.

Spending down your assets is one of the biggest issues facing retirees today. To be honest, saving for retirement isnt all that hard. By buying a well-diversified, low-cost, mostly equity portfolio, the market is going to do most of the work. Where the real challenge lies is in unsaving or spending down these same assets in retirement. But how do we go about doing that? You have to be aware of things like income and capital gains taxes and their effects on your returns as well as on your spendable income. As the old saying goes, its not what you earn, its what you take home. What about the make-up of your portfolio? Become more conservative is an all too familiar mantra of advisors. But what does that mean? Does it mean having fewer equities? More bonds? What risk are investors avoiding, and more importantly, what risk is it creating for them? In particular, longevity risk the risk of outliving your savings!

In a traditional portfolio, retiring at the wrong time, which can impact sequence of return risk, can have a disastrous effect on whether or not you have enough money to maintain your standard of living in retirement. Losing money in the first few years of retirement, combined with retirees tending to living longer, or longevity risk, can create a perfect storm for those nearing or in retirement. You must have a plan to mitigate that risk.

By having a formal income distribution plan in place, retirees can address the primary issues surrounding them today such as:

1. What assets to spend in which order

2. Integrating Social Security claiming strategies into an income plan

3. Risk control in a portfolio, including longevity, sequence of return and volatility

4. Low interest rates

5. Taxes

Having a formal income distribution plan in place can potentially help retirees have a more enjoyable retirement.

T. Eric Reich, CIMA, CFP, CLU, ChFC is president and founder of Reich Asset Management and can be reached at 609-486-5073 or eric@reichassetmanagement.com.

Securities offered through Kestra Investment Services, LLC (Kestra IS), member FINRA/SIPC. Investment advisory services offered through Kestra Advisory Services, LLC (Kestra AS), an affiliate of Kestra IS. Reich Asset Management, LLC is not affiliated with Kestra IS or Kestra AS. The opinions expressed in this commentary are those of the author and may not necessarily reflect those held by Kestra Investment Services, LLC or Kestra Advisory Services, LLC. This is for general information only and is not intended to provide specific investment advice or recommendations for any individual. It is suggested that you consult your financial professional, attorney, or tax advisor with regard to your individual situation.

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How to live a long, productive life, according to a 102-year-old who just released his first album – CNBC

December 15th, 2019 7:43 am

"I know I'm mad about you, and all but lost without you, and great affection for you I proclaim.... But baby, there's an issue I just can't remember your name."

So goes the chorus of "I Just Can't Remember Your Name," on the 10-track album, "Senior Song Book" released in November. The lyrics are a humorous nod to a common pain point about aging. After all, the song's writer, Alan R. Tripp, is 102.

What's more, it's Tripp's first album.

"People ask me how did I live so long and have my mind clicking away," he told NPR's "All Things Considered." "The answer is you do not retire from something. You retire to something," said Tripp. "And your life will continue with any luck."

That's exactly what Tripp who has had multiple careers, including as a radio news broadcaster, an advertising executive and a businessman has been doing. Though, for the record, he considers himself "semi-retired," according to a promotional interview he did with his publicist.

Still, Tripp's lastest foray into music production wasn't entirely planned.

When Tripp was 99, he wrote a poem called "Best Old Friends" about the new friendships he had made at Beaumont at Bryn Mawr, the Pennsylvania retirement community where he lives. Marvin Weisbord, 88, who lives at Beaumont too, turned the poem into a song for Tripp's 100th birthday.

That song catalyzed the album. Weisbord plays piano on the album, and the two produced it at a local recording studio.

Marvin Weisbord (L) set a poem his friend, Alan Tripp, wrote to music for Tripp's 100th birthday. That catalyzed the album.

Photo courtesy Lisa Schaeffer Photography

Now that the CD has dropped (and is on back-order at CDBaby as of Friday), the centenarian is planning his next move.

"I was writing a book when this thing came up," Tripp told NPR. So that will be his next endeavor.

"It's a mystery book. I've written several other books, but never a mystery. So when I'm done with this, back to the computer and write that mystery book," Tripp told NPR. (Tripp published one book in 1992, one in 2006 and a third in 2015.)

Japanese longevity expert, Dr. Shigeaki Hinohara, who lived to be 105, also said the key to a long, happy life was to stay active.

"There is no need to ever retire, but if one must, it should be a lot later than 65," Hinohara told The Japan Times in 2009.

From the age of 65, Hinohara worked 18-hour days, seven days a week as a volunteer and "love[d] every minute of it," he said. In fact, he volunteered until the last few months before his death on July 18, 2017, according to The New York Times.

Fashion icon, Iris Apfel, 98, is also still working. She released the book "Accidental Icon" in 2018 and still juggles any number of fashion collaborations, including a line with The Home Shopping Network.

"For me, retirement is a fate worse than death," she told Money in 2018 after her book release. "I've seen so many people, especially in a place like Palm Beach, who worked so hard in their lives, and they come down here cold turkey, and then one day wake up and they realize how vacuous their lives are now. I mean it isn't funny, I've seen it with my own eyes!"

Tripp seems to agree: "If you retire to slothfulness, believe me you'll be a slob," he said in a promotional interview he did with his publicist. "That's all that will happen to you."

See also:

This Japanese longevity expert lived to 105 here's what he ate every day

95-year-old fashion icon Iris Apfel says hard work is her fountain of youth

Iris Apfel: 10 life lessons from a 96-year-old who is probably cooler than you

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Study with centenarians finds novel protein signature of protective APOE genotype – National Institute on Aging

December 15th, 2019 7:43 am

A novel protein signature may have the potential to serve as a biomarker for resistance to Alzheimers disease and cognitive decline, according to a new study with a group of centenarians and their offspring. The researchers found a correlation between 16 proteins found in blood and the 2 form of the apolipoprotein E (APOE) gene. The study, led by investigators at Boston University in collaboration with the NIA Intramural Research Program and Novartis, was reported in Aging Cell.

Having the 2 form of the APOE gene is thought to be neuroprotective, whereas having the 4 form is associated with increased risk of late-onset Alzheimers disease and poor cognitive function. The 2 form, which is much rarer than 4, is more commonly detected among those over 100 years old and their children than in the general population. APOE 2 also seems to promote longevity, but the precise biological mechanisms for it being neuroprotective and promoting long life are not known.

Because recent studies showed that APOE-associated protein products can be found in blood serum samples, the researchers analyzed serum to find the biological products of APOE 2. Serum was collected from 222 people in the NIA-supported New England Centenarian Study, including 51 with APOE 2.

Using a protein profiling platform to analyze several thousand proteins in serum that corresponded to more than 4,000 genes, the researchers found that 16 proteins were associated with different APOE genotypes. They explored the different gene expression profiles of 16 proteins in brains of people with late-onset Alzheimer's disease and healthy controls and showed that the signatures were significantly different between the two groups.

Next, they confirmed their findings by repeating the analysis with serum and plasma samples from other cohort studies. Finally, they examined the association between the 16 proteins and changes in cognitive function in the centenarians and found that seven of these proteins correlate with patterns of cognitive function.

If future studies show that the signature proteins are driving cognitive health, rather than merely being associated with it, these proteins could serve as biomarkers in intervention studies targeting APOE 2. In addition, the protein signature identified in this study could be developed into an early detection test of resistance to developing Alzheimers.

This research was supported in part by the NIA Intramural Research Program; NIA grants U19AG023122, R21AG056630 and R01AG061844; and NIH contracts 263 MD 9164 and 263 MD 821336.

Reference: Sebastiani P, et al. A serum protein signature of APOE genotypes in centenarians. Aging Cell. 2019;18(6):e13023. doi: 10.1111/acel.13023.

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The immune system did its job – Haaretz

December 15th, 2019 7:42 am

The fact that Israel has to hold a third election within such a short period of time reflects a grave political crisis. The fact that millions of people will again be exposed to wasteful, inflammatory and uncontrolled advertising campaigns is also far from ideal. And yet, it also carried a reassuring message for everyone who champions healthy democracy.

In fact, Israel must go to the polls again because the system of checks and balances that is the foundation of democracy worked. It prevented, in every manner possible, a situation in which a prime minister who has been charged with criminal offenses, who seeks to escape to the city of refuge of parliamentary immunity, continues to serve.

Killing Palestinians isnt Israels goal. Killing Palestine is. Listen

Since that is exactly what Benjamin Netanyahu attempted and is still attempting to do, it would have been wrong to give in to the natural desire to get it over with that is, to establish any sort of government and return to the appearance of proper governance. The establishment of a government is a means, not an end in itself. It is supposed to reflect the wills and the needs of the voters, and it is not supposed to serve as a refuge for a prime minister who has been charged with criminal offenses.

Therefore, there is also no call for the lamentation and the cries of shame surrounding the failure to form a government. On the contrary: its a badge of honor for the parliamentary immune system, which disgorged from itself the possibility of collaborating with the forces seeking to sabotage Israels democratic infrastructure from within.

Kahol Lavan should be commended for resisting the temptation to join Netanyahu for a promise of half the kingdom, and in so upheld its election-eve promises to its voters. Yisrael Beiteinu Chairman Avigdor Lieberman is also deserving of praise, for consistently opposing a narrow immunity government. Amir Peretz of Labor-Gesher should be lauded for keeping his word and for not setting his sights on power for even a moment.

Like a short-circuiting electrical appliance with the potential for disaster, the Knesset dissolved itself after it became clear that its only path forward entailed riding roughshod over fundamental democratic values.

In order to reset the main circuit breaker so as to turn on the light switch once more, all of the political parties that view themselves as guided by the rule of law must join forces and focus on the next election, and tell Netanyahu in the clearest manner possible that his time is up.

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The above article is Haaretzs lead editorial, as published in the Hebrew and English newspapers in Israel.

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The immune system did its job - Haaretz

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Study finds differences in energy use by immune cells in ME/CFS – National Institutes of Health

December 15th, 2019 7:42 am

News Release

Thursday, December 12, 2019

NIH-funded research suggests changes in the immune system in myalgic encephalomyelitis/chronic fatigue syndrome.

New findings published in the Journal of Clinical Investigation suggest that specific immune T cells from people with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) show disruptions in the way they produce energy. The research was supported by the National Institutes of Health.

This research gives us additional evidence for the role of the immune system in ME/CFS and may provide important clues to help us understand the mechanisms underlying this devastating disease, said Vicky Whittemore, Ph.D., program director at NIHs National Institute of Neurological Disorders and Stroke (NINDS), which partially funded the study.

ME/CFS is a severe, chronic, and debilitating disease that can cause a range of symptoms including pain, severe exhaustion, cognitive impairment, and post-exertional malaise, the worsening of symptoms after physical or mental activity. Estimates suggest that between 836,000 and 2.5 million people in the United States may be affected by ME/CFS. It is unknown what causes the disease and there are no treatments.

Research by Alexandra Mandarano and collaborators in the laboratory of Maureen Hanson, Ph.D., professor of molecular biology and genetics at Cornell University in Ithaca, New York, examined biochemical reactions involved in energy production, or metabolism, in two specific types of immune cells obtained from 45 healthy controls and 53 people with ME/CFS. Investigators focused on CD4 T cells, which alert other immune cells about invading pathogens, and CD8 T cells, which attack infected cells. Dr. Hansons team used state-of-the-art methods to look at energy production by the mitochondria within T cells, when the cells were in a resting state and after they had been activated. Mitochondria are biological powerhouses and create most of the energy that drives cells.

Dr. Hanson and her colleagues did not see significant differences in mitochondrial respiration, the cells primary energy-producing method, between healthy and ME/CFS cells at rest or after activation. However, results suggest that glycolysis, a less efficient method of energy production, may be disrupted in ME/CFS. Compared to healthy cells, CD4 and CD8 cells from people with ME/CFS had decreased levels of glycolysis at rest. In addition, ME/CFS CD8 cells had lower levels of glycolysis after activation.

Our work demonstrates the importance of looking at particular types of immune cells that have different jobs to do, rather than looking at them all mixed together, which can hide problems specific to particular cells, said Dr. Hanson. Additional studies focusing on specific cell types will be important to unravel whats gone wrong with immune defenses in ME/CFS.

Dr. Hansons group also looked at mitochondrial size and membrane potential, which can indicate the health of T cell mitochondria. CD4 cells from healthy controls and people with ME/CFS showed no significant differences in mitochondrial size nor function. CD8 cells from people with ME/CFS showed decreased membrane potential compared to healthy cells during both resting and activated states.

Dr. Hansons team examined associations between cytokines, chemical messengers that send instructions from one cell to another, and T cell metabolism. The findings revealed different, and often opposite, patterns between healthy and ME/CFS cells, suggesting changes in the immune system. In addition, the presence of cytokines that cause inflammation unexpectedly correlated with decreased metabolism in T cells.

This study was supported in part by the NIHs ME/CFS Collaborative Research Network, a consortium supported by multiple institutes and centers at NIH, consisting of three collaborative research centers and a data management coordinating center. The research network was established in 2017 to help advance research on ME/CFS.

In addition to providing valuable insights into the immunology of ME/CFS, we hope that the results coming out of the collaborative research network will inspire more researchers, particularly those in the early stages of their careers, to work on this disease, said Joseph Breen, Ph.D., section chief, Immunoregulation Section, Basic Immunology Branch, National Institute of Allergy and Infectious Diseases (NIAID), which partially funded the study.

Future research studies will examine metabolism in other subsets of immune cells. In addition, researchers will investigate ways in which changes in metabolism affect the activity of T cells.

This study was supported by NINDS grant U54NS105541, NIAID grant R21AI117595, Simmaron Research, and an anonymous private donor.

NINDS (https://www.ninds.nih.gov/) is the nations leading funder of research on the brain and nervous system.The mission of NINDS is to seek fundamental knowledge about the brain and nervous system and to use that knowledge to reduce the burden of neurological disease.

About the National Institutes of Health (NIH):NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit http://www.nih.gov.

NIHTurning Discovery Into Health

Mandarano et al. Myalgic encephalomyelitis/chronic fatigue syndrome patients exhibit altered T cell metabolism and cytokine associations, Journal of Clinical Investigation. December 12, 2019

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Study finds differences in energy use by immune cells in ME/CFS - National Institutes of Health

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The new tool in fighting cancer: Antibiotics – Penn: Office of University Communications

December 15th, 2019 7:42 am

The antibiotic vancomycin alters the gut microbiome in a way that can help prime the immune system to more effectively attack tumor cells after radiation therapy. A new study in mice from researchers at theAbramson Cancer Center found giving a dose of the common antibiotic not only helped immune cells kill tumors that were directly treated with radiation, but also kill cancer cells that were further away in the body, paving the way for researchers to test the approach in a human clinical trial. The findings are published inTheJournal of Clinical Investigation.

In recent years, multiple studies have shown that giving patients higher doses of radiation over the course of fewer treatmentscalled hypo-fractionated radiotherapycan induce a stronger immune response in patients. In addition, hypo-fractionated doses have the ability to impact other tumors cells in the body that werent directly treated with radiation. This is known as the abscopal effect.

Our study shows that vancomycin seems to boost the effect of the hypo-fractionated radiation itself on the targeted tumor site while also aiding the abscopal effect, helping the immune system fight tumors away from the treatment site, says the studys senior authorAndrea Facciabene, an associate professor of radiation oncology at the Perelman School of Medicine.

Facciabene and his team chose vancomycin for a few specific reasons. First, it mostly targets gram-positive bacteria, making it disruptive to the gut microbiome. Second, its a large molecule, which means it stays in the gut and does not circulate to the rest of the body the way other antibiotics do. The fact that it is not systemic limits the impact it has on the rest of the bodys microbiome.

Read more at Penn Medicine News.

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The new tool in fighting cancer: Antibiotics - Penn: Office of University Communications

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New molecule for rheumatoid arthritis may be effective in preventing cartilage destruction – The Hindu

December 15th, 2019 7:42 am

A specific fragment of a protein secreted by the parasitic worm liver fluke (Fasciola) has been found to protect the articular cartilage of joints from being destroyed by the bodys aberrant immune system, thus preventing rheumatoid arthritis from progressing. Besides protecting the cartilage from further destruction, the team of researchers from the Central Drug Research Institute (CSIR-CDRI) also found that the protein prevented the joint bone from being destroyed. In rheumatoid arthritis, the joint bone starts getting destroyed following cartilage destruction.

Liver flukes secrete certain specialised proteins that help the parasites to evade recognition by the host immune system and also blunt the killing machinery of the immune system by dialling down the inflammatory responses.

The protein Fasciola helminth defence molecule-1 (FhHDM-1) secreted by liver fluke has similarity with a human protein that mitigates inflammatory responses. So the team led by Naibedya Chattopadhyay isolated a specific fragment of this protein having a high anti-inflammatory function. They then synthesised and tested it in a cell culture system followed by animal testing.

The results were published in FASEB Journal.

A mouse model that is vulnerable to rheumatoid arthritis was used for testing the protective effect of the protein. The type-II collagen protein the major component present in the cartilage matrix of the joints but not as a whole protein seen in blood was introduced in large quantities to trigger an autoimmune response. With this, the process of cartilage destruction was set in motion.

Twenty days after introducing the antigen protein to trigger an autoimmune response, the researchers introduced the synthesised peptide every second day to evaluate its potential to protect the collagen from destruction. The peptide rapidly stopped further damage to the cartilage. The cartilage that has already been damaged was not repaired because the damage is irreversible in the case of rheumatoid arthritis, says Yasir Akhtar Khan from the Department of Zoology at the Aligarh Muslim University, Aligarh, and the first author of the paper. Besides preventing cartilage destruction, the peptide also prevented the joint bone from destruction.

The cartilage of animals that only received the type II collagen but not the peptide was completely destroyed by the end of the experiment (46 days), while the cartilage of the treatment group that received the peptide for four weeks was protected from further damage.

The effect of treatment in controlling cartilage destruction was assessed externally during the course of treatment by measuring paw swelling every day. By 25 days of treatment, there was complete abolition of paw swelling compared with the diseased animals that did not receive any treatment, says Dr. Khan. All the animals were sacrificed at the end of 46 days and the joints examined.

There was extensive structural damage to the cartilage in mice that did not receive the peptide. The barrier that insulates the cartilage was destroyed leading to disease progression, he says. In the treatment group, the barrier was intact and comparable to the control group that did not have rheumatoid arthritis. We also did not see any immune cells in the joints of the treated animals.

In contrast to the currently used anti-rheumatic drug (methotrexate), the biggest advantage of using the liver fluke peptide is that it does not produce a wholesale suppression of the immune system. Even the monoclonal antibodies that act against individual inflammatory molecules have inherent problems. For instance, the monoclonal antibodies target and suppress the tumour necrosis factor (TNF alpha), which is the first line of defence against Mycobacterium. In the Indian context, the anti-rheumatic drug and even the monoclonal antibodies that target TNF alpha will leave the person susceptible to infections, including TB.

The liver fluke peptide only produces selective protection to the joints and does not alter the systemic immune system. So the bodys ability to combat bacterial pathogens will remain intact. Dr. Chattopadhyay says. We are yet to study the mechanism of selective joint protection (cartilage and bone) provided by the peptide.

Thus, in the Indian scenario, the peptide that specifically prevents joint inflammation and destruction without affecting the bodys overall immune function might prove a game-changer in treating rheumatoid arthritis if further tests and trials find it effective.

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New molecule for rheumatoid arthritis may be effective in preventing cartilage destruction - The Hindu

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