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Global Stem Cell and Platelet Rich Plasma Alopecia Therapies Market 2019 Analysis forecast to 2024 Focusing on Top Key Players Orange County Hair…

December 17th, 2019 8:44 am

The Report Stem Cell and Platelet Rich Plasma (PRP) Alopecia TherapiesMarket provides Key Benefits, Key Market Segments, Secondary and Primary Research, Analyst Tools and Models to 2024. The report will assist reader with better understanding and decision making.

GlobalStem Cell and Platelet Rich Plasma (PRP) Alopecia TherapiesMarketpresented byMRInsights.bizexamines market ecosystem, adoption trends, key drivers, competitive outlook, key challenges, restraints, market share, revenue, opportunities, future growth potentials, and revenue chain analysis. The report delivers data on manufacturers, geographical regions, types, applications. Key players are evaluated considering various parameters like product portfolio, product scope, revenue, share, company overview, sales, contact information, market share from 2013 to2024. Its a must-read for entrepreneurs, investors, consultants, researchers and those who are planning to boost their business in theStem Cell and Platelet Rich Plasma (PRP) Alopecia Therapiesmarket.

DOWNLOAD FREE SAMPLE REPORT:https://www.mrinsights.biz/report-detail/213867/request-sample

The worldwide market is an enlarging field for top market players :Orange County Hair Restoration Center, Hair Sciences Center of Colorado, Evolution Hair Loss Institute, Savola Aesthetic Dermatology Center, Anderson Center for Hair, Colorado Surgical Center & Hair Institute, Virginia Surgical Center, Hair Transplant Institute of Miami

Regional section of this report covers the investigation of various parameters such as production volume, revenue, profit margin, export-import figures, and local consumption in different regional markets. Regions that have been covered for this market:Americas (United States, Canada, Mexico, Brazil), APAC (China, Japan, Korea, Southeast Asia, India, Australia), Europe (Germany, France, UK, Italy, Russia, Spain), Middle East & Africa (Egypt, South Africa, Israel, Turkey, GCC Countries)

Each segment is comprehensively studied in the report concerning market acceptance, market trends, consumption tendencies, profitability, attractiveness, and revenue generation.Drivers and restraints look at the external factors assisting and controlling the growth of the market.Other major covered in this report includes market status (2013-2019), advantages and disadvantages of enterprise products, competition pattern, regional characteristics, industry development trends, industrial policy, and macroeconomic policies. The report mainly focuses on delivering competitive advantages to market players which will help them compete vigorously in the ever-changing business environment.

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Research objectives

There are 13 Chapters to deeply display the globalStem Cell and Platelet Rich Plasma (PRP) Alopecia Therapiesmarket.

Chapter 1:Scope of the Report

Chapter 2:Executive Summary

Chapter 3:GlobalStem Cell and Platelet Rich Plasma (PRP) Alopecia Therapiesby Manufacturers

Chapter 4:Stem Cell and Platelet Rich Plasma (PRP) Alopecia Therapiesby Regions

Chapter 5, 6, 7, 8 and 9:Americas,APAC,Europe,Middle East & Africa,Market Drivers, Challenges and Trends

Chapter 10 and 11:Marketing, Distributors and CustomerAndGlobalStem Cell and Platelet Rich Plasma (PRP) Alopecia TherapiesMarket Forecast.

Chapter 12 And 13 :Key Players Analysis,Research Findings and Conclusion.

Customization of the Report:This report can be customized to meet the clients requirements. Please connect with our sales team (sales@mrinsights.biz), who will ensure that you get a report that suits your needs.

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Global Stem Cell and Platelet Rich Plasma Alopecia Therapies Market 2019 Analysis forecast to 2024 Focusing on Top Key Players Orange County Hair...

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Synthetic Stem Cells Market 2019 Global Trend, Segmentation And Opportunities Forecast To 2025 – Space Market Research

December 17th, 2019 8:44 am

Global Synthetic Stem Cells Market Size, Status and Forecast 2019-2025offers a primary overview of the Synthetic Stem Cells industry coveringDefinition, Classification, Industry Value, Price, Cost and Gross Profit, Share via Region, New Challenge Feasibility Evaluation, Analysis and Guidelines on New mission Investment. Synthetic Stem Cells Market report presents in-intensity insight ofCompany Profile, Capacity, Product Specifications, Production Value, Sales, Revenue, Price, Gross Margin, Market Size and Market Sharesfor topmost prime key vendors(North Carolina State University, Zhengzhou University). In the end, there are 4 key segments covered in this Synthetic Stem Cells market report: competitor segment, product type segment, end use/application segment and geography segment.

Target Audience of Synthetic Stem Cells Market:Suppliers, Channel Partners,Production Companies, Market Consultants,Marketing Authorities, Research Institutions, Subject Matter Experts, Financial Institutions, Government Authorities.

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Synthetic Stem Cells Market Summary:Synthetic stem cells offer therapeutic benefits comparable to those from natural stem cells and could reduce some of the risks associated with stem cell therapies. Additionally, these cells have better preservation stability and the technology is generalizable to other types of stem cells.

Based on Classifications,each type is studied as Sales, Synthetic Stem Cells Market Share (%), Revenue (Million USD), Price, Gross Margin and more similar information.each type, including:

Cardiovascular Diseases Neurological Disorders Other Diseases

Based on the end users/applications,this report focuses on the status and outlook for major applications/end users, sales volume, Synthetic Stem Cells market share and growth rate of Synthetic Stem Cells foreach application, including:

Cancers Wounds and Injuries Musculoskeletal Disorders Blood disorders

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Synthetic Stem Cells Market: Regional Analysis Includes:

Industrial Chain, Sourcing Strategy and Downstream Buyers (2019 2025)

Synthetic Stem Cells Market Capacity, Production, Revenue, Consumption, Export and Import (2019 2025)

Synthetic Stem Cells Market Forecast (2019 2025)

Contact:

ResearchMozMr. Nachiket Ghumare,Tel: +1-518-621-2074USA-Canada Toll Free: 866-997-4948Email:[emailprotected]

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Synthetic Stem Cells Market 2019 Global Trend, Segmentation And Opportunities Forecast To 2025 - Space Market Research

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Stem Cell Therapy for Osteoarthritis Market 2019 by Research, Statistics, Review and Growth to 2025 – Downey Magazine

December 17th, 2019 8:44 am

The Stem Cell Therapy for Osteoarthritis market report [6 Year Forecast 2019-2025] focuses on Major Leading Industry Players, providing info like Stem Cell Therapy for Osteoarthritis market competitive situation, product scope, market overview, opportunities, driving force and market risks. Profile the top manufacturers of Stem Cell Therapy for Osteoarthritis, with sales, revenue and global market share of Stem Cell Therapy for Osteoarthritis are analyzed emphatically by landscape contrast and speak to info. Upstream raw materials and instrumentation and downstream demand analysis is additionally administrated. The Stem Cell Therapy for Osteoarthritis market business development trends and selling channels square measure analyzed. From a global perspective, It also represents overall industry size by analyzing qualitative insights and historical data.

The study encompasses profiles of major companies operating in the global Stem Cell Therapy for Osteoarthritis market. Key players profiled in the report includes : Mesoblast, Regeneus, U.S. Stem Cell, Anterogen, Asterias Biotherapeutics and so on.

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This Stem Cell Therapy for Osteoarthritis market report provides a comprehensive analysis of:Industry overview, manufacturing cost structure analysis, technical data and manufacturing plants analysis, major manufacturers analysis, development trend analysis, overall market overview, regional market analysis, consumers analysis and marketing type analysis.

Scope of Stem Cell Therapy for Osteoarthritis Market:

The global Stem Cell Therapy for Osteoarthritis market is valued at million US$ in 2018 and will reach million US$ by the end of 2025, growing at a CAGR of during 2019-2025. The objectives of this study are to define, segment, and project the size of the Stem Cell Therapy for Osteoarthritis market based on company, product type, application and key regions.

This report studies the global market size of Stem Cell Therapy for Osteoarthritis in key regions like North America, Europe, Asia Pacific, Central & South America and Middle East & Africa, focuses on the consumption of Stem Cell Therapy for Osteoarthritis in these regions.

This research report categorizes the global Stem Cell Therapy for Osteoarthritis market by players/brands, region, type and application. This report also studies the global market status, competition landscape, market share, growth rate, future trends, market drivers, opportunities and challenges, sales channels, distributors, customers, research findings & conclusion, appendix & data source and Porters Five Forces Analysis.

The end users/applications and product categories analysis:

On the basis on the end users/applications,this report focuses on the status and outlook for major applications/end users, sales volume, market share and growth rate of Stem Cell Therapy for Osteoarthritis foreach application, including-

On the basis of product,this report displays the sales volume, revenue (Million USD), product price, Stem Cell Therapy for Osteoarthritis market share and growth rate ofeach type, primarily split into-

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Stem Cell Therapy for Osteoarthritis Market : The Regional analysis covers:

The Crucial Questions Answered by Stem Cell Therapy for Osteoarthritis Market Report:

The report offers exclusive information about the Stem Cell Therapy for Osteoarthritis market, based on thorough research about the macro and microeconomic factors that are instrumental in the development of the market. The information featured in this report can answer salient questions for companies in the Stem Cell Therapy for Osteoarthritis market, in order to make important business-related decisions. Some of these questions include:

And Many More.Contact Us:

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Stem Cell Therapy for Osteoarthritis Market 2019 by Research, Statistics, Review and Growth to 2025 - Downey Magazine

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Stem Cell Antibody Market Expected to Deliver Dynamic Progression until 2028|Thermo Fisher Scientific, Inc. (US) – Industry News Info

December 17th, 2019 8:44 am

The Stem Cell Antibody Market report gives an astonishing source to analyze the Stem Cell Antibody market and other fundamental subtleties identifying with it. The examination uncovers the general evaluation and associated ideas of the Stem Cell Antibody market. The report displays a reasonable scenario of the Stem Cell Antibody market, that links applications, proposals, industry chain structure, and definitions. Likewise, it connects the expansive validity of the Stem Cell Antibody market and configurations to a fundamental precision, experiences, and industry-substantiated estimations of the general Stem Cell Antibody market. Additionally, the examination underlines the huge driving business players (Thermo Fisher Scientific, Inc. (U.S.), Merck Group (Germany), Abcam plc (U.K.), Becton, Dickinson and Company (U.S.), Bio-Rad Laboratories, Inc. (U.S.), Cell Signaling Technology, Inc. (U.S.), Agilent Technologies, Inc. (U.S.), F. Hoffmann-La Roche Ltd (Switzerland), Danaher Corporation (U.S.), GenScript (U.S.), PerkinElmer, Inc. (U.S.), Lonza (Switzerland), and BioLegend, Inc. (U.S.)) across the globe with clear affiliation profiles, data of the wide-ranging business, item type, conditions, and courses of action.

The Stem Cell Antibody market report more focuses on top industry leaders and explores all essentials facets of competitive landscape. It explains potent business strategies and approaches, consumption propensity, regulatory policies, recent moves taken by competitors, as well as potential investment opportunities and market threats also. The report emphasis crucial financial details of major manufacturers including year-wise sale, revenue growth, CAGR, production cost analysis, and value chain structure.

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The manufacturing base, Stem Cell Antibody Industry chain view, raw material cost, labor cost, and downstream buyers analysis is represented. The production and market share by type and application from 2019-2025 are presented in this study. Also, the consumption ratio, gross margin analysis, and import-export statistics are portrayed. The market status and SWOT analysis for different regions and countries are profiled in this report.

Global Stem Cell Antibody Market: Type Outlook:Primary Antibodies, Secondary Antibodies

Global Stem Cell Antibody Market: Application Outlook:Proteomics, DrugDevelopment, Genomics

North America (United States, Canada)Europe (Germany, France, UK, Italy, Russia, Spain)Asia Pacific (China, Japan, Korea, India, Australia, New Zealand)Middle East & Africa (Middle East, Africa)Latin America (Mexico, Brazil, C. America, Chile, Peru, Colombia)

Furthermore, the report provides the core knowledge of the market by analyzing end users consumption tendency, Stem Cell Antibody market driving factors, ever-changing market dynamics, and rising development patterns in the market.

Besides, the report focuses on the leading contenders in the Stem Cell Antibody industry and delivers an all-inclusive analysis considering their market share, production capacity, value chain analysis, size, sales and distribution network, import/export activities, cost structure, and product specification. Due to the changes in world business policies, it is recommended to be always aware of the facts and data about this market.

The study objectives of this report are:

1) To share detailed information about the key factors influencing the growth of the market (growth potential, opportunities, drivers, industry-specific challenges and risks).2) To understand the structure of the Stem Cell Antibody market by identifying its various sub-segments.3) The marketing strategies, opportunities, and Stem Cell Antibody development factors are explained.4) The competitive landscape structure, market size estimation, recent advancements in the industry are explained.5) The market dynamics, competition, and complete insights will lead to profitable business plans.6) The pricing structure covering the labor cost, raw material cost, capacity, and supply-demand statistics are presented.

The key dynamic factors that are detailed in the report:

Key Market Dynamics: The Global Stem Cell Antibody Market research report details the latest industry trends, growth patterns, and research methodologies. The factors that directly contribute to the growth of the market include the production strategies and methodologies, development platforms, and the product model itself, wherein a small change would result in further changes in the overall report. All of these factors are explained in detail in the research study.

Market Outlook: The report also sheds light on some of the major factors, including R&D, new product launches, M&A, agreements, partnerships, joint ventures, collaborations, and growth of the key industry participants, on a regional and global basis.

Major Features: The report provides a thorough analysis of some of the significant factors, which include cost, capacity, capacity utilization rate, production, revenue, production rate, consumption, import/export, supply/demand, gross, market share, CAGR, and gross margin. Besides, the report provides a comprehensive study of the key influencing factors and market inclinations, in addition to the relevant market segments and sub-segments.

Analytical Tools: The Global Stem Cell Antibody Market report consists of the precisely studied and evaluated information of the key players and their market scope using several analytical tools, including SWOT analysis, Porters five forces analysis, investment return analysis, and feasibility study. These tools have been used to efficiently study the growth of major industry participants.

Potential Customers: The report offers detailed insights to users, service providers, suppliers, manufacturers, stockholders, and individuals who are interested in evaluating and self-studying this market.

Inquiry for Buying Report: http://www.marketsnresearch.com/inquiry-for-buying.html?repid=50557

Conclusively, the report helps a reader to get an absolute understanding of the Stem Cell Antibody industry through details about the market projection, competitive scenario, industry environment, growth constraining factors, limitations, entry barriers, the provincial regulatory framework as well as upcoming market investment and opportunities, challenges and other growth-promoting factors. This report will provide you a clear view of each and every facet of the market without a need to refer to any other research report or a data source. Our report will provide you with all the facts about the past, present, and future of the concerned Market.

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Stem Cell Antibody Market Expected to Deliver Dynamic Progression until 2028|Thermo Fisher Scientific, Inc. (US) - Industry News Info

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CPAP Systems Market Outlook, Opportunity and Demand Analysis 2019 to 2025| ResMed, Philips Respironics, Company three – Uncovering News

December 17th, 2019 8:44 am

Global CPAP Systems Market Overview:

The latest report on the global CPAP Systems market suggests a positive growth rate in the coming years. Analysts have studied the historical data and compared it with the current market scenario to determine the trajectory this market will take in the coming years. The investigative approach taken to understand the various aspects of the market is aimed at giving the readers a holistic view of the global CPAP Systems market. The research report provides an exhaustive research report that includes an executive summary, definition, and scope of the market.

Get PDF template of CPAP Systems market report@ https://www.qyresearch.com/sample-form/form/1102066/global-CPAP-Systems-market

Report in Detail

CPAP is an acronym for Continuous Positive Airway Pressure. It provides the same (continuous) level of pressure to the persons upper airway all night.The global CPAP Systems market was xx million US$ in 2018 and is expected to xx million US$ by the end of 2025, growing at a CAGR of xx% between 2019 and 2025.

This report studies the CPAP Systems market size (value and volume) by players, regions, product types and end industries, history data 2014-2018 and forecast data 2019-2025; This report also studies the global market competition landscape, market drivers and trends, opportunities and challenges, risks and entry barriers, sales channels, distributors and Porters Five Forces Analysis.

Geographically, this report is segmented into several key regions, with sales, revenue, market share and growth Rate of CPAP Systems in these regions, from 2014 to 2025, covering

North America (United States, Canada and Mexico)Europe (Germany, UK, France, Italy, Russia and Turkey etc.)Asia-Pacific (China, Japan, Korea, India, Australia, Indonesia, Thailand, Philippines, Malaysia and Vietnam)South America (Brazil etc.)Middle East and Africa (Egypt and GCC Countries)

The various contributors involved in the value chain of the product include manufacturers, suppliers, distributors, intermediaries, and customers. The key manufacturers in this market include

ResMedPhilips RespironicsCompany threeDeVilbiss HealthcareApexTeijin PharmaMedtronic (Covidien)Koike MedicalFosun PharmaBMC Medical

By the product type, the market is primarily split into

Fixed Pressure CPAP DeviceAuto Adjusting CPAP Device

By the end users/application, this report covers the following segments

HospitalHome CareOthers

We can also provide the customized separate regional or country-level reports, for the following regions:

North AmericaUnited StatesCanadaMexicoAsia-PacificChinaIndiaJapanSouth KoreaAustraliaIndonesiaSingaporeMalaysiaPhilippinesThailandVietnamRest of Asia-PacificEuropeGermanyFranceUKItalySpainRussiaRest of EuropeCentral & South AmericaBrazilRest of Central & South AmericaMiddle East & AfricaGCC CountriesTurkeyEgyptSouth AfricaRest of Middle East & Africa

The study objectives of this report are:To study and analyze the global CPAP Systems market size (value & volume) by company, key regions/countries, products and application, history data from 2014 to 2018, and forecast to 2025.To understand the structure of CPAP Systems market by identifying its various subsegments.To share detailed information about the key factors influencing the growth of the market (growth potential, opportunities, drivers, industry-specific challenges and risks).Focuses on the key global CPAP Systems manufacturers, to define, describe and analyze the sales volume, value, market share, market competition landscape, SWOT analysis and development plans in next few years.To analyze the CPAP Systems with respect to individual growth trends, future prospects, and their contribution to the total market.To project the value and volume of CPAP Systems submarkets, with respect to key regions (along with their respective key countries).To analyze competitive developments such as expansions, agreements, new product launches, and acquisitions in the market.To strategically profile the key players and comprehensively analyze their growth strategies.

In this study, the years considered to estimate the market size of CPAP Systems are as follows:History Year: 2014-2018Base Year: 2018Estimated Year: 2019Forecast Year 2019 to 2025

This report includes the estimation of market size for value (million USD) and volume (K Units). Both top-down and bottom-up approaches have been used to estimate and validate the market size of CPAP Systems market, to estimate the size of various other dependent submarkets in the overall market. Key players in the market have been identified through secondary research, and their market shares have been determined through primary and secondary research. All percentage shares, splits, and breakdowns have been determined using secondary sources and verified primary sources.

For the data information by region, company, type and application, 2018 is considered as the base year. Whenever data information was unavailable for the base year, the prior year has been considered.

Key StakeholdersRaw material suppliersDistributors/traders/wholesalers/suppliersRegulatory bodies, including government agencies and NGOCommercial research & development (R&D) institutionsImporters and exportersGovernment organizations, research organizations, and consulting firmsTrade associations and industry bodiesEnd-use industries

Available CustomizationsWith the given market data, QYResearch offers customizations according to the companys specific needs. The following customization options are available for the report:Further breakdown of CPAP Systems market on basis of the key contributing countries.Detailed analysis and profiling of additional market players.

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The report is a perfect example of a detailed and meticulously prepared research study on the global CPAP Systems market. It can be customized as per the requirements of the client. It not only caters to market players but also stakeholders and key decision makers looking for extensive research and analysis on the global CPAP Systems market.

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CPAP Systems Market Outlook, Opportunity and Demand Analysis 2019 to 2025| ResMed, Philips Respironics, Company three - Uncovering News

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Can diabetes cause anxiety? Blood sugar and other causes – Medical News Today

December 17th, 2019 8:43 am

Many people with diabetes also experience anxiety, and they may wonder whether there is a link between the two conditions.

Diabetes and anxiety are both among the leading causes of disability in developed countries around the world.

In the United States alone, anxiety affects close to 40 million adults. Diabetes is also common, with about 30.3 million U.S. adults living with this condition.

A 2013 meta-analysis revealed that people with diabetes face a higher likelihood than the general population of experiencing anxiety.

In this article, we outline the reasons for this association. We also describe the symptoms of both diabetes and anxiety, as well as how healthcare professionals diagnose each of these conditions.

People with diabetes are responsible for managing their blood sugar levels and ensuring that these stay within a healthy range. This task can be challenging and stressful.

Doctors will ask people with diabetes to remain mindful of their blood sugar levels and to engage in routine behaviors, such as:

Planning, checking, and being prepared for a wide range of challenges are all important for effective diabetes management. However, some people may worry excessively about their blood sugar levels or how their disease may progress. These concerns may trigger episodes of anxiety.

According to the National Library of Medicine, anxiety is "excessive worry or fear at real or imagined situations."

The emotional challenges of living with diabetes can also trigger anxiety.

Researchers report that anxiety affects about 40% of people with diabetes. This prevalence is much higher than that in the general U.S. population, where the condition affects 18.1% of people.

People with diabetes are at risk of developing low blood sugar, or hypoglycemia. Some of the symptoms of hypoglycemia are identical to those of anxiety.

Additionally, the results of a 2015 animal study suggest that experiencing several episodes of hypoglycemia can increase the likelihood of anxiety. The reason for this may be that hypoglycemic episodes trigger chemical and metabolic changes that physically affect the part of the brain that plays a role in processing anxiety.

The procedures that healthcare professionals use to diagnose diabetes and anxiety are quite different.

According to the Centers for Disease Control and Prevention (CDC), doctors diagnose diabetes using one or more of the following blood tests:

A person should see their doctor if they think that they have anxiety. The doctor may ask the person to fill in a questionnaire that asks about their psychological and physical symptoms.

In some cases, a doctor may refer the person for a mental health screening with a psychiatrist or psychotherapist. These mental health professionals will be able to carry out a more detailed assessment.

People with diabetes and anxiety must learn to distinguish between rational concerns over diabetes management and irrational, anxious thinking.

The first step in this process is to work closely with healthcare professionals to develop a diabetes treatment plan. This plan should include information on the following:

For people with anxiety, many different treatment options are available. A doctor or mental health professional may recommend one or more of the following approaches:

The combination of diabetes and anxiety can create a vicious cycle of physical and emotional problems. However, people who learn to manage their anxiety may find themselves better able to manage their diabetes.

Certain lifestyle practices can be beneficial for people with diabetes, anxiety, or both. These include:

Diabetes and anxiety are two serious yet common conditions, which can share some of the same symptoms.

People with diabetes are at increased risk of developing anxiety because they may experience excessive fear and worry about the management and possible progression of diabetes. Concerns over the physical symptoms themselves can also trigger anxiety.

Anxiety can, in turn, interfere with a person's ability to manage their blood sugar levels. Due to this, a person who has diabetes should see their doctor if they begin to experience symptoms of anxiety.

Many treatment options are available to help people deal with the symptoms of diabetes and anxiety. Certain lifestyle changes may also help with the management of both conditions.

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Can diabetes cause anxiety? Blood sugar and other causes - Medical News Today

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Could Liraglutide Stall the Onset of Type 2 Diabetes in Kids? – Medscape

December 17th, 2019 8:43 am

LOS ANGELES Until the recentapprovalofliraglutidefor the treatment of children and adolescents with type 2 diabetes, investigators likeSonia Caprio, MD,were at their wits' end watching the beta-cell function of their patients decline on metformin treatment.

"The kids were not doing well. It was like they were being treated with water," Dr. Caprio, a pediatric endocrinologist at Yale University, New Haven, Conn., said at the annual World Congress on Insulin Resistance, Diabetes and Cardiovascular Disease.

For example, in the NIH-fundedTODAY(Treatment Options for Type 2 Diabetes in Adolescents and Youth) study thatbegan enrollment in 2004, 699 patients aged between 10 and 17 years and with type 2 diabetes were treated with metformin (1,000 mg, twice daily) to attain a glycated hemoglobin level of less than 8% and were then randomly assigned to continued treatment withmetforminalone or to metformin combined with rosiglitazone (4 mg, twice a day) or a lifestyle-intervention program that focused on weight loss through modifying eating and activity behaviors (N Engl J Med. 2012;366:2247-56).

Over the course of 11 months, the researchers found that 46% of the children were failing treatment. "The worst arm was the metformin arm," said Dr. Caprio, who was involved with the study. "Kids were not responding to the drug at all. About 52% of children failed to do better using metformin a classic drug that we all start kids on when we diagnose them with type 2 diabetes."

Findings from a follow-up study,TODAY2, showed that these young patients were prone to serious diabetes-related events, such as heart attacks, chronic kidney disease, retinal disease, neuropathy, and complications in the offspring of pregnancies.

In addition, results from theRISE(Restoring Insulin Secretion) Pediatric Medication Study found that, in youth with impaired glucose tolerance or recently diagnosed type 2 diabetes, neither 3 months of insulin glargine followed by 9 months of metformin nor 12 months of metformin alone halted the progressive deterioration of beta-cell function (Diabetes Care. 2018;41:1717-25).

"The uniqueness ofRISEis that we employed very sophisticated techniques to measure insulin secretion and sensitivity while they were being treated with these usual drugs," said Dr. Caprio, who was one of the study investigators. "The beta cell is unresponsive to metformin and other treatments. The question is, why?"

Despite these findings, 2018 consensus guidelines from the American Diabetes Association on the evaluation and management of youth-onset diabetes (Diabetes Care. 2018;41:2648-68) call for the administration of metformin twice daily in youth with new-onset diabetes who have a hemoglobin A1c(HbA1c)level of less than 8.5%. "I argue that is not the way. We need better ways to treat [these patients] because they are moving fast to having complications," she said.

Enter theEllipse Trial, a pivotal multicenter, randomized study that evaluated the effect of the glucagonlike peptide-1 receptor agonist liraglutide in children and adolescents with type 2 diabetes (N Engl J Med. 2019;381:637-46).

Researchers, led byWilliam V. Tamborlane, MD, chief of Yale Medicine Pediatric Endocrinology, also in New Haven, randomized 135 patients to one of two arms: 66 to subcutaneous liraglutide (up to 1.8 mg/day) and 69 to placebo for a 26-week, double-blind period, followed by a 26-week open-label extension period. All patients received metformin during the trial. More than half of the study participants (62%) were female, the mean age was 15 years, 65% were white, the mean body mass index was 33.9 kg/m2, their mean fasting glucose was 8.4 mmol/L, and their mean HbA1cwas 7.8%.

At 26 weeks, the mean glycated hemoglobin level had decreased by 0.64 percentage points with liraglutide and increased by 0.42 percentage points with placebo,for an estimated treatment difference of 1.06 percentage points (Pless than .001). By 52 weeks, the difference increased to 1.30 percentage points.

"There was also a significant drop in BMIzscore in patients treated with liraglutide, which is important," Dr. Caprio said. "This medication is having an impact on weight, which is a key driver of the onset of type 2 diabetes in youth. This is a remarkable achievement because weight loss is hard to achieve in obese adolescents, as we showed in the TODAY study."

The number of adverse events reported by patients was similar in the treatment and placebo groups (85% and 81%, respectively), but the overall rates of adverse events and gastrointestinal adverse events were higher with liraglutide.

"I use liraglutide just for weight reduction because I mainly see a lot of kids with obesity. Many kids are not responding because of the GI effects of this drug. I think the weight loss could have been better had the investigators moved to a dose of 1.8 mg, which we use in adults."

A fasting plasma glucose of 6.1 mmol/L was the primary reason for participants remaining on a lower dose of liraglutide, she said. At the same time, liraglutide concentration data indicated a high rate of noncompliance, which was expected in this population. "That's a big problem we face with children," Dr. Caprio said. "Some of them are not constantly taking the medication. They skip doses a lot. But that happens with patients in this age group."

"Finally, we have something else to help children and teenagers to delay the complications we are seeing," Dr. Caprio said. "To me, I think this is a new era. I have hope. It will be interesting to see whether liraglutide and perhaps SGLT2 [sodium-glucose transporter 2] inhibitors can delay the onset of type 2 diabetes in children. In my view, we will be doing this with drugs. I don't think the weight loss [concerns are] going to go away without medication, unfortunately."

Dr. Caprio reported having no financial disclosures.

This article originally appeared on MDEdge.com.

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Could Liraglutide Stall the Onset of Type 2 Diabetes in Kids? - Medscape

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Frustrated With Cumbersome, Clunky Diabetes Devices, Patients Are Turning To DIY Technology – Kaiser Health News

December 17th, 2019 8:43 am

Many feel like the tools available on the market werent built by people actually living with the disease, and so those with technology experience are taking matters into their own hands. In other health and technology news: virtual reality, the data Catch-22, prosthetics, cyberattacks, and Apple's push into the health industry.

The Washington Post:DIY Diabetes Tech Gains Popularity With Patients And Parents Fed Up With Clunky Mainstream Medical DevicesOne night, 18-month-old Hazel Lumpkin woke up with her diaper completely soaked with urine. Her parents, Matt and Melody Lumpkin of Pasadena, Calif., rediapered her in a larger size, hoping that would fix the issue. But Hazel continued to saturate diaper after diaper. As a childhood fan of The Baby-Sitters Club a book series featuring a young girl with Type 1 diabetes Melody recalled the connection between frequent urination and diabetes in children. (Kim, 12/14)

The Washington Post:Virtual Reality, Robots, Interactive Apps, Other New Tech Help People With Dementia And Their CaretakersDoris Moss has always loved dancing. Now in her 80s and suffering from a form of dementia, it has become more important than ever, as hearing a good beat will spur her to get up and move around. And so her daughter, Angela Pearson, who lives with her mother in Ellenwood, Ga., and is her primary caretaker, has turned to a new technology for people with Alzheimers and other forms of dementia: a touch-screen application known as SimpleC Companion, that can be set to play some of Mosss favorite music along with recorded reminders to drink water and take medication at various points of the day when Pearson is away from the house. (Kalter, 12/15)

The Washington Post:Data Catch-22: How Tech Gadgets For Exercise Sometimes Do More Harm Than GoodWhen Bri Cawsey began running in 2008, she quickly got hooked on the sport and wanted to get faster. So she did what many runners do and bought a GPS watch that would give her real-time feedback on her pace, mileage and other metrics. First, she enjoyed the data readout. Before long, she connected her watch to an app that helped her track calories, as well. Then she added a second watch, more sophisticated than the first, and began comparing the data from the two for better accuracy. By about 2012, Cawsey found she couldnt do anything without a tracking watch on her wrist. (Loudin, 12/14)

The Washington Post:New Prosthetic Can Help People Who Have Lost A Limb Feel Again, And May Reduce Phantom PainPhantom pain was all that Keven Walgamott had left of the limb he lost in an accident over a decade ago until he tried on the LUKE Arm for the first time in 2017, and told researchers that he could feel again. The arm is a motorized and sensorized prosthetic that has been in development for over 15 years by a team at the University of Utah. Researchers around the world have been developing prosthetics that closely mimic the part of the human body they would replace. (Dhar, 12/14)

The Associated Press:Large Hospital System Says It Was Hit By Ransomware AttackNew Jerseys largest hospital system said Friday that a ransomware attack last week disrupted its computer network and that it paid a ransom to stop it. Hackensack Meridian Health did not say in its statement how much it paid to regain control over its systems but said it holds insurance coverage for such emergencies. (12/13)

The Wall Street Journal:New Jersey Hospital System Hit By CyberattackAttacks on hospitals and health systems, who have been digitizing their operations and record-keeping, have proven to be hugely disruptive, in some cases leaving small physician groups unable to recover. Victims have been forced to cancel some elective procedures, shut down computer networks to prevent further spread of the virus and temporarily revert to using paper records. (Evans, 12/13)

Stat:7 Startups Acquired By Apple That Are Central To Its Health StrategyThe Apple Watch continuously monitors numerous health metrics and doubles as a virtual clinical trial site. AirPods, Apples wireless ear buds, function as basic hearing aids, and its health record app lets users pull in data from health care providers. ...Over the past decade, Apple has nabbed roughly half a dozen startups with specialties that could prove critical for health care disruption, from speech recognition and sleep tracking to health record consolidation and hospital mapping. (Brodwin, 12/16)

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Top 10 diabetes home remedies that tame your blood sugar levels – TheHealthSite

December 17th, 2019 8:43 am

Scientists from various parts of the world involved in a $6 million dollar study have come up with an interesting revelation: Long-term remission from type 2 diabetes is possible just by losing 1 gram of fat from the pancreas. While this finding comes as a surprise to many, there are some facts about blood sugar that we are all aware of. Type 2 diabetes has a strong association with your lifestyle. What you eat determines your susceptibility to this condition and also, how well you can manage it.

Type 2diabetesaffects the bodys ability to either produce insulin or to use insulin effectively, you need treatment to keep your blood sugar levels within a normal range. Although there are numerous treatment options available to keep your blood sugar levels in control, home remedies can work wonders in achieving this task. Here are top 10 effective home remedies to maintain your blood sugar levels and lead a healthy life with diabetes.

The leaves of holy basil are packed with antioxidants and essential oils that produce eugenol, methyl eugenol and caryophyllene. Collectively these compounds help the pancreatic beta cells (cells that store and release insulin) to function properly and increase sensitivity to insulin. An added advantage is that the antioxidants present in the leaves help beat the ill effects of oxidative stress.

Tip: Consume two to three tulsi leaves whole or about one tablespoon full of its juice on an empty stomach to lower the blood sugar levels. Here are top 10 health benefits of tulsi.

Due to their high fibre content flaxseeds help digestion and aid in the proper absorption of fats and sugars. Consuming flax seed helps reduce a diabetics postprandial sugar level by almost 28 percent.

Tip: Consume one tablespoon of ground flaxseed powder every morning on an empty stomach with a glass of warm water. However, do not have more than 2 tablespoons per day, as it can be detrimental to your health. Here are 11 ways to include flaxseeds in your diet.

The leaves of bilberry have been used in Ayurveda for many centuries to control diabetes. Recently, the Journal of Nutrition stated that the leaves of the Bilberry plant contain high amounts of anthocyanidin, which enhance the action of various proteins involved in glucose transportation and fat metabolism. Due to this unique property, bilberry leaves are a great way to lower ones blood sugar levels.

Tip: Crush bilberry leaves in a mortar and pestle and consume 100 milligrams of this extract every day on an empty stomach.

Also known as dalchini, it improves insulin sensitivity and lower blood glucose levels. Having as little as teaspoon of cinnamon per day can improve ones insulin sensitivity and help controlling weight, thereby decreasing ones risk for heart disease.

Tip: Include about 1 gram of dalchini into your daily diet for about a month to help lower blood sugar levels. Read more health benefits of cinnamon.

Unlike other tea leaves, green tea is unfermented and is high in polyphenol content. Polyphenol is a strong antioxidant and hypo-glycaemic compound that helps control the release of blood sugars and helps the body use insulin better. Read more 10 types of flavoured green tea that have 20 health benefits.

Tip: Steep a bag of green tea in hot water for 2-3 minutes. Remove the bag and drink a cup of this tea in the morning or before your meals.

Also called moringa, the leaves of this plant are best known for their ability to boost ones energy. These have also been declared a superfood. In the case of diabetics, the moringa leaf increases satiety and slows the breakdown of food and lower blood pressure.

Tip: Take a few drumstick leaves, wash and crush them to extract their juice. Now take about 1/4th cup of this juice and drink it on an empty stomach, every morning to keep your sugar levels under control.

Also known as psyllium husk is often used as a laxative. When isabgol comes in contact with water, it swells to form a gel-like substance. This slows the breakdown and absorption of blood glucose. Isabgol also protects the stomach lining from ulcers and acidity.

Tip: Cosume isabgol after every meal, ideally with milk or water. Avoid having it with curd as it can lead to constipation. Read in detail about 8 health benefits of isabgol or psyllium husk you didnt know.

Bitter gourd is rich in plant insulin-polypeptide-P, a bio-chemical that mimics the insulin produced by the human pancreas and thus, reduces sugar levels in the body. It is also known to be highly beneficial for diabetics owing to thetwo very essential compounds called charatin and momordicin, which are the key compounds in lowering ones blood sugar levels.

Tip: Consume karela at least once a week either as a subzi or in a curry. If you want quick results, try having a glass of karela juice on an empty stomach once in three days. Read more about 8 healthy reasons to drink bittergourd or karela juice!

Found abundantly in India, the bitter leaf has a number of amazing medicinal properties. Neem enhances insulin receptor sensitivity, helps improve blood circulation by dilating the blood vessels, lowers blood glucose levels and reduces ones dependence on hypoglycemic drugs. Here are more health benefits of neem.

Tip: Drink the juice of the tender shoot of neem leaves on an empty stomach for best results.

A glycoside present in the seeds of Indian blackberry prevents the conversion of starch to sugar. It lowers blood sugar and helps prevent insulin spikes. Jambul also has properties that can protect you from heart diseases and other vascular disorders.

Tip: Eat around 5 6 jamuns in the morning to control your blood sugar levels. Alternatively, you can also add a spoonful of jamun seeds powder to a glass of warm water or milk and drink this daily for better control of diabetes.

Published : December 16, 2019 4:10 pm | Updated:December 17, 2019 11:06 am

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People with diabetes should get annual eye exams it’s very possible that vision loss can be preventable – User-generated content

December 17th, 2019 8:43 am

People with diabetes are at increased risk ofdevelopingseriouseye diseases, yet most do not have sight-saving annual eyeexams,accordingtoalargestudy.

TheKentucky Academy of Eye Physicians and Surgeonsjoins theAmerican Academy of Ophthalmologyin reiterating the importance of eye exams.

Researchers at Wills Eye Hospital in Philadelphia have found that more than half of patientswith the disease skip these exams. They also discovered that patients who smoke and those with less severe diabetes and no eye problems were mostlikely to neglect having these checks.

The researcherscollaborated with the Centers for DiseaseControl and Prevention toreviewthe charts of close to 2,000 patientsage 40 or older with type 1and type 2 diabetes to see how many had regular eye exams.Their findings over a four-year period revealed that:

Fifty-eight percent of patients did not have regularfollow-upeye exams. Smokers were20 percent less likelyto have exams. Thosewith less-severe disease and no eye problems were least likely tofollow recommendations. Those who had diabetic retinopathy were 30 percent more likely to have follow-up exams.

One in 10 Americans have diabetes, putting them at heightened risk for visual impairment due to the eye diseasediabetic retinopathy.The diseasealso can lead to other blinding ocular complications if not treated in time.Fortunately, having adilated eye exam yearly or more often can prevent 95 percent of diabetes-related visionloss.

Eye exams are critical as they can reveal hidden signs of disease, enabling timely treatment.This is why the Academy recommends people with diabetes have them annually or more often as recommended by their ophthalmologist, a physician who specializes in medical and surgical eye care.

Vision loss is tragic, especially when it is preventable, said Ann P. Murchison, M.D., M.P.H., lead author of the study and director of the eye emergency department at Wills Eye Hospital. Thats whywe want to raise awareness and ensure people with diabetes understand the importance ofregular eye exams.

The Academy offers thisanimated public service announcementto help educate people about the importance of regular exams and common eye diseases including diabetic retinopathy. It encourages the public to watch and share it with their friends and family.

People with diabetes need to know that they shouldnt wait until they experience problems to get these exams, Rahul N. Khurana, M.D, clinical spokesperson for the Academy. Getting your eyes checked by an ophthalmologist can reveal the signs of disease that patients arent aware of.Diabetic retinopathy, much like glaucoma, can be insidious in its ability to cause vision loss, said Thomas Harper, M.D., an ophthalmologist in Louisville.

It is common to have diabetic retinopathy without having any symptoms.Once symptoms manifest, retinopathy can be quite advanced.Even though it is a bit of an oversimplification, there are two types of people who go blind from diabetes: those who dont control his or her diabetes, and those who dont go to the eye doctor. Schedule your retina exam today.

Kentucky Academy of Eye Physicians and Surgeons

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AINsight: Diabetes and Flying | Business Aviation – Aviation International News

December 17th, 2019 8:43 am

Diabetes Mellitus is a disease that involves impaired glucose metabolism. Sudden adverse changes in blood glucose (high or low) can lead to altered mental status, to seizures, and even death. Long-term complications include damage to end organs, such as eyes, kidneys, heart, and the neurological system.

Further, this is a condition that would renderan existing medical certificate invalid from the moment the pilot knew of the diagnosis, regardless of any theoretical period of validity that might appear to remain for that certificate.

Are all pilots with diabetes grounded indefinitely? Is there any hope for a pilot with diabetes to fly again? What about commercially?

The answers are reassuring. Private pilots with well-controlled diabeteshave been flying for many years. And a recently implemented program with the support of the Federal Air Surgeon will now enable even more diabetics to return to commercial flying.

Without going into an elaborate explanation of itsphysiology, lets break diabetes down into two categories: non-insulin-dependent and insulin-dependent.

Insulin is a hormone that is released by the pancreas in response to blood glucose levels. All body tissues use glucose for energy. When blood glucose rises, the pancreas secretes insulin, permitting the bodily tissues to store and use glucose for various metabolic functions.

In certain cases of diabetes, the production of insulin is significantly decreased or completely absent. Common names include juvenile, type 1, or insulin-dependent diabetes (IDDM). Dont let the term juvenile confuse the situation, as there are times when insulin dependence might not occur until well into adulthood.

The relevant premise here is that the body has stopped producing sufficient insulin to regulate blood glucose, regardless of the persons age. You might also see the term insulin-treated diabetes (ITDM) in various publications, and for the purposes of FAA medical certification, IDDM and ITDM can be used synonymously.

In other cases, the bodily tissues have become resistant to the insulin that the pancreas is dutifully producing (obesity is a common cause of insulin resistance). Terms familiar to most people include adult-onset, type 2, or non-insulin-dependent diabetes.

Google mellitus for the amusing reference of how that word became part of the lore of diabetes centuries ago. I will provide more pathophysiologic information when I discuss the individual types of diabetes and the respective FAA certification programs more specifically in future submissions.

Therefore, I wont go into the formalities and minutia of how to diagnose, treat, and monitor diabetes in this discussion. Suffice it to say that poorly-controlled diabetes poses a significant threat to aviation safety, not to mention long-term health.

Diabetes that can be controlled with diet, exercise, and weight loss is the proverbial no-brainer in FAA medical certification. Anything a pilot can do without medical intervention is always preferable for long-term health maintenance.

All classes of medical certificates can be easily obtained in this setting and usually a special issuance is not required (at times this is followed through a slightly amended protocol for pre-diabetes that Ill discuss at a future date).

The necessity for oral and some of the injectable non-insulin medications that lower blood glucose to control diabetes also does not preclude FAA medical certification. In this case, while the pilot will be followed under a special issuance authorization, all classes of medical certificates are again included in this protocol. I have had many pilots flying commercially on first- and second-class medical certificates for many years who are taking oral diabetic medications.

If a pilot requires insulin, however, things change. Before 1996, any insulin-dependent pilot was unable to fly (all classes of medical certificates were excluded). Beginning in 1996, pilots could obtain a third-class FAA medical certificate if they are taking insulin and their diabetes is well controlled.

Fortunately, the program for third-class IDDM pilots has been a great success. The very rare adverse in-flight incidents over the years with diabetic pilots usually have occurred in pilots with poorly controlled diabetes who likely would not havebeen granted a special issuance authorization in the first place.

A pilot who requires insulin for treatment has been excluded for classes of FAA medical certificates higher than third-class until just recently. I have been a vocal advocate to the FAA and its various Federal Air Surgeons over the years that well-controlled IDDM pilots should be considered for first- and second-class certification.

With the current precise continuous glucose monitoring (CGM) electronics and advancements available, an insulin-dependent diabetic is now able to maintain tightly-controlled blood glucose levels.

In 2002, Canada began permitting IDDM pilots to fly commercially in a multi-pilot crew environment. The UK began doing so in 2012, and now the U.S. joined that group last month (on November 7).

Notably, there is no restriction in the FAA protocol that an IDDM pilot must be in a crew environment. Thus, an FAA-licensed pilot with a special issuance for IDDM can fly single-pilot so long as all provisions are met. The FARs dont permit the FAA to put restrictions such as must be part of a multi-pilot crew on first-class medical certificates.

There are also several other countries that permit private flying in pilots with various forms of diabetes.

As you can imagine, the FAA was very cautious and reviewed the advances in diabetic management technologies methodically over many years before authorizing this new program. No different than any other special issuance program, the FAA did not want aviation accidents resulting from a poorly conceived program.

This would, of course, be a tragedy for anyone involved in the accident and could jeopardize the entire program itself. Out of respect for caution, the FAA spent many years working on this program. And now, its finally here!

However, the requirements are probably the most extensive of any special issuance program that we have. There will be ongoing evaluations of numerous organ systems. In addition to using the latest technology to monitor and treat a pilot's diabetes, evaluations will be ongoing for eyes, heart, kidneys, and neurological systems.

The data presentation to the FAA is also extensive and thorough. As with some of the other special issuance conditions, the FAA has developed comprehensive checklistsfor pilots, their AMEs, and the treating physiciansand flow sheets to assist in the detailed data presentation to the FAA. Ongoing CGM data will also be required.

As exhaustive as this program is, it has finally opened the world of commercial flying to IDDM pilots who require a first- or second-class FAA medical certificate. I am hopeful that the program will be as successful as the earlier program for third-class pilots has been.

Those with IDDM are often some of the most motivated pilots there are, and the new gadgetry involved has demonstrated to the FAA that precise control of diabetes can indeed be achieved and, therefore, such pilots do not pose a threat to aviation safety. Thus, it is predicted that IDDM pilots will be able to fly safely in commercial operationson first- and second-class special issuance authorizationsin the U.S.

For a pilot to obtain a special issuance authorization under this new IDDM protocol, they will need an organized and motivated team of support. The pilot, first and foremost, must adequately control their diabetes using modern electronics, including CGM devices, as that also will improve the likelihood of maintaining long-term health.

Next, the treating physician must be willing to complete thorough FAA flow sheets and, at select times, consulting physicians will have to provide evaluation data of the other organ systems mentioned above. Finally, the AME must be willing to choreograph all of the data into a packet that will be acceptable to the FAA.

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Your feet need special treatment when you have diabetes – The Oakland Press

December 17th, 2019 8:43 am

There are an estimated 30.3 million people with diabetes in the United States, with approximately 7.2 million individuals not aware they have the disease.

Uncontrolled diabetes poses a major threat to vital organs and other body tissues, which heal more slowly because of the disease.

Diabetes is the inability to manufacture or properly use insulin, impairing the bodys ability to regulate sugar (glucose) levels which provide energy to cells and tissues throughout the body. Therefore, it is a disease that affects many parts of the body and is associated with serious complications such as heart disease, stroke, blindness, kidney failure and lower limb amputations. The leading cause of hospitalization among people with diabetes is foot ulcers and infections, but most of those problems are largely preventable.

More than 60 percent of all nontraumatic lower-limb amputations worldwide are related to complications from the disease, according to the American Diabetes Association. For that reason, the Michigan Podiatric Medical Association (MPMA) has tips to help diabetic patients take better care of their feet.

While is it extremely important for those with diabetes to receive regular foot exams by a podiatrist, keeping feet healthy to remain active can often prevent one from developing Type 2 diabetes, says Jodie Sengstock, DPM, MPMA director of professional relations. Our feet are our foundation. Keeping them healthy improves quality of life.

While there is no cure for diabetes, patients can live with it well. A person with diabetes may enjoy a full and active life with proper diet, exercise, medical care and careful management at home.

Managing and treating the disease requires a team of specialists including a primary care physician, endocrinologist, ophthalmologist, dentist, vascular surgeon and podiatrist.

Podiatrists are trained to treat foot conditions that can be caused by diabetes, such as: neuropathy, infection and ulcers.

While ulcers open sores are the most common diabetes-related foot problem, several others are also serious and prevalent, including neuropathy (pain or numbness), skin changes, poor circulation and infection. The nerve damage that diabetes causes may mean a person with an ulcer or injury may be unaware of it until it becomes infected. Regular care from a podiatrist can reduce amputation rates up to 80 percent, according to research of the American Podiatric Medical Association.

Here are some tips for home management:

People with diabetes should inspect their feet daily and look vigilantly for signs of ulcers, including irritation, redness, cracked or dry skin especially around the heels or body fluid, such as blood, on their socks.

Discuss diabetes and the risks with family members. Diabetes can be hereditary, so talk to family members about monitoring blood sugar and foot health.

Never go barefoot. Always protect feet with the proper footwear and make sure socks and shoes are comfortable and fit well.

Trim toenails straight across, and never cut the cuticles. Seek immediate treatment for ingrown toenails, as they can lead to serious infection.

Never try to remove calluses, corns or warts by yourself. Over-the-counter products can burn the skin and cause irreparable damage to the foot.

Exercise. Walking can keep weight down and improve circulation. Be sure to wear appropriate athletic shoes.

Keep feet elevated while sitting.

Wear thick, soft socks. Avoid socks with seams, which can rub and cause blisters or other skin injuries.

Have new shoes properly measured and fitted. Foot size and shape often changes over time. Shoes that fit properly should not rub or cause irritation.

Wiggle toes and move feet and ankles up and down for five-minute sessions throughout the day.

Visit an MPMA podiatrist regularly at least two times per year to avoid unnecessary complications.

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Do Women With Diabetes Need More CVD Risk Reduction Than Men? – Medscape

December 17th, 2019 8:43 am

BUSAN, SOUTH KOREA Whether cardiovascular disease risk reduction efforts should be more aggressive in women than men with the diabetes depends on how you interpret the data.

Two experts came to differentconclusions on this question during a heated, but jovial, debate last week here at the International Diabetes Federation 2019 Congress.

Endocrinologist David Simmons, MB BChir, Western Sydney University, Campbelltown, Australia, argued that diabetes erases the well-described life expectancy advantage of 4-7 years that women experience over men in the general population.

He also highlighted the fact that the heightened risk is of particular concern in both younger women and those with prior gestational diabetes.

But Timothy Davis, BMedSc MB BS, DPhil, an endocrinologist and general physician at Fremantle Hospital, Western Australia, countered that the data only show the diabetes-attributable excess cardiovascular risk is higher among women than men, but that the absolute risk is actually greater in men.

Moreover, he argued, at least in type 1 diabetes, there's no evidence that more aggressive cardiovascular risk factor management improves outcomes.

Simmons began by pointing out that although, on average, women die at an older age than men, it has been known for over 40 years that this "female protection" is lost among insulin-treated women, particularly as a result of their increased risk for cardiovascular disease.

In a 2015 meta-analysis of 26 studies, women with type 1 diabetes were found to have about a 37% greater risk of all-cause mortality compared to men with the condition when mortality is contrasted with that of the general population, and twice the risk of both fatal and nonfatal vascular events.

The risk appeared to be greater among women who were younger at the time of diabetes diagnosis. "This is a really important point the time we would want to intervene," Simmons said.

In another meta-analysis of 30 studies including 2,307,694 individuals with type 2 diabetes and 252,491 deaths, the pooled women-to-men ratio of the standardized mortality ratio for all-cause mortality was 1.14.

In those with versus without type 2 diabetes, the pooled standardized mortality ratio in women was 2.30 and in men was 1.94, both significant compared to those without diabetes.

And in a 2006 meta-analysis of 22 studies involving individuals with type 2 diabetes, the pooled data showed a 46% excess relative risk using standardized mortality ratios in women versus men for fatal coronary artery disease.

Meanwhile, in a 2018 meta-analysis of 68 studies involving nearly 1 million adults examining differences in occlusive vascular disease, after controlling for major vascular risk factors, diabetes roughly doubled the risk for occlusive vascular mortality among men (relative risk, 2.10), but tripled it among women (3.00).

Women with diabetes aged 35-59 years had the highest relative risk for death over follow-up across all age and sex groups: they had 5.5 times the excess risk compared to those without diabetes, while the excess risk for men of that age was 2.3-fold.

"So very clearly, it's these young women who are most at risk, "emphasized Simmons, whois an investigator for Novo Nordisk and a speaker for Medtronic, Novo Nordisk, and Sanofi.

The question has arisen whether the female/male differences might be because of differences in cardiovascular risk factor management, Simmons noted.

A 2015 American Heart Association (AHA) statement laid out the evidence for lower prescribing of statins, aspirin, beta-blockers, and angiotensin-converting enzyme (ACE) inhibitors among women compared with men, Simmons said.

And some studies suggest medication adherence is lower in women than men.

In terms of medications, fenofibrate appears to produce better outcomes in women than men, but there is no evidence of gender differences in the effects of statins, ACE inhibitors, or aspirin, Simmons said.

He also outlined the results of a 2008 study of 78,254 patients with acute myocardial infarction from 420 US hospitals in 2001-2006.

Women were older, had more comorbidities, less often presented with ST-elevation myocardial infarction (STEMI), and had a higher rate of unadjusted in-hospital death (8.2% vs 5.7%; P < .0001) than men. Of the partcipants, 33% of women had diabetes compared with 28% of men.

The in-hospital mortality difference disappeared after multivariable adjustment, but women with STEMI still had higher adjusted mortality rates than men.

"The underuse of evidence-based treatments and delayed reperfusion among women represent potential opportunities for reducing sex disparities in care and outcome after acute myocardial infarction," the authors concluded.

"It's very clear amongst our cardiology colleagues that something needs to be done and that we need more aggressive cardiological risk reduction in women," Simmons said.

"The AHA has already decided this. It's already a policy. So why are we having this debate?" he wondered.

He also pointed out that women with prior gestational diabetes are an exceptionally high-risk group, with a two-fold excess risk for cardiovascular disease within the first 10 years postpartum.

"We need to do something about this particularly high-risk group, independent of debates about gender," Simmons emphasized. "Clearly, women with diabetes warrant more aggressive cardiovascular risk reduction than men with diabetes, especially at those younger ages," he concluded.

Davis began his counter argument by stating that estimation of absolute vascular risk is an established part of strategies to prevent cardiovascular disease, including in diabetes.

And that risk, he stressed, is actually higher in men.

"Male sex is a consistent adverse risk factor in cardiovascular disease event prediction equations in type 2 diabetes. Identifying absolute risk is important," he said, noting risk calculators include male sex, such as the risk engine derived from the United Kingdom Prospective Diabetes Trial.

And in the Australian population-based Fremantle study, of which Davis is an author, the absolute 5-year incidence rates for all outcomes including myocardial infarction, stroke, heart failure, lower extremity amputation, cardiovascular mortality, and all-cause mortality were consistently higher in men versus women in the first phase, which began in the 1990s and included 1426 individuals with diabetes (91% had type 2 diabetes).

In the ongoing second phase, which began in 2008 with 1732 participants, overall rates of those outcomes are lower and the discrepancy between men and women has narrowed, Davis noted.

Overall, the Fremantle study data "suggest that women with type 2 diabetes do not need more aggressive cardiovascular reduction than men with type 2 diabetes because they are not at increased absolute vascular risk," he stressed.

And in a "sensitivity analysis" of two areas in Finland, the authors concluded that the stronger effect of type 2 diabetes on the risk of CHD in women compared with men was in part explained by a heavier risk factor burden and a greater effect of blood pressure and atherogenic dyslipidemia in women with diabetes, he explained.

The Finnish authors wrote, "In terms of absolute risk of CHD death or a major CHD event, diabetes almost completely abolished the female protection from CHD."

But, Davis emphasized, rates were not higher in females.

So then, "Why is there the view that women with type 2 diabetes need more aggressive cardiovascular risk reduction than men with diabetes?"

"It probably comes back to confusion based on absolute risk versus a comparison of relative risk within each sex," he asserted.

Lastly, in a meta-analysis published just in July this year involving more than 5 million participants, compared to men with diabetes, women with diabetes had a 58% and 13% greater risk of CHD and all-cause mortality, respectively.

"This points to an urgent need to develop sex- and gender-specific risk assessment strategies and therapeutic interventions that target diabetes management in the context of CHD prevention," the authors concluded.

But, Davis noted, "It is not absolute vascular risk. It's a relative risk compared across the two genders. In the paper, there is no mention of absolute vascular risk."

"Greater CVD mortality in women with and without diabetes, versus men, doesn't mean there's also an absolute vascular increase in women versus men with diabetes," he said.

Moreover, Davis pointed out that in an editorial accompanying the 2015 meta-analysis in type 1 diabetes, Simmons had actually stated that absolute mortality rates are highest in men.

"I don't know what happened to his epidemiology knowledge in the last 4 years but it seems to have gone backwards," he joked to his debate opponent.

And, Davis asserted, even if there were a higher risk in women with type 1 diabetes, there is no evidence that cardiovascular risk reduction measures affect endpoints in that patient population. Only about 8% of people with diabetes in statin trials had type 1 diabetes.

Indeed, he noted, in the American Diabetes Association (ADA) Standards of Medical Care in Diabetes 2019, the treatment goals for individual cardiovascular risk factors do not mention gender.

What's more, David said, there is evidence that women are significantly less likely than men to take prescribed statins and are more likely to have an eating disorder and underdose insulin, "suggesting significant issues with compliance...So, trying to get more intensive risk reduction in women may be a challenge."

"Women with diabetes do not need more aggressive cardiovascular risk reduction than men with diabetes, irrespective of type," he concluded.

International Diabetes Federation 2019 Congress. December 5, 2019.

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Number of people in Turkey with diabetes rising: expert – Anadolu Agency

December 17th, 2019 8:43 am

ANTALYA, Turkey

More people in Turkey are being diagnosed with diabetes compared with previous years, an expert said Sunday.

Speaking to the media, Tugbay Tug, a professor at Ankara Universitys Faculty of Medicine, Department of General Surgery, said the number of people in Turkey with diabetes now accounts for more than 10% of the population compared with 7% five years ago.

Tug underlined that Turkey is the third highest country in Europe in terms of the number of diabetes patients.

About half of the patients with diabetes are losing their feet because of foot wounds, he said.

The mortality rate of patients who have lost one organ is much higher than the mortality rate caused by most lethal cancers, and 50% die within three years, he added.

Tug warned that diabetes should not be ignored.

One out of 10 people in society are diabetes patients and the number of people with diabetes totals more than 8 million in Turkey, he added.

He said 20% of Turkeys population will have diabetes by 2025 if people dont change their dietary habits.

Scientific data shows that one in four diabetes patients suffer foot wounds. We can say that there are at least 2 million diabetic foot patients in Turkey. This number will increase if we dont live healthy.

*Writing by Davut Demircan

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Detection of Secondary Metabolites as Biomarkers for the Early Diagnos | DMSO – Dove Medical Press

December 17th, 2019 8:42 am

Jumana Y Al-Aama,1,2 Hadiah B Al Mahdi,1 Mohammed A Salama,1 Khadija H Bakur,1,2 Amani Alhozali,3 Hala H Mosli,3 Suhad M Bahijri,4 Ahmed Bahieldin,5,6 Lothar Willmitzer,7 Sherif Edris1,5,6

1King Abdulaziz University, Princess Al Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, Jeddah, KSA; 2King Abdulaziz University Faculty of Medicine, Department of Genetic Medicine, Jeddah, KSA; 3King Abdulaziz University, Faculty of Medicine, Department of Endocrinology and Metabolism, Jeddah, KSA; 4King Abdulaziz University, Faculty of Medicine, Department of Clinical Biochemistry, Jeddah, KSA; 5King Abdulaziz University, Faculty of Science, Biological Sciences Department, Jeddah, KSA; 6Ain Shams University, Department of Genetics, Cairo, Egypt; 7Max-Planck-Institut Fr Molekulare Pflanzenphysiologie, Molecular Physiology, Golm, DE, Germany

Correspondence: Sherif Edris; Jumana Y Al-AamaKing Abdulaziz University, Princess Al Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, Jeddah, KSATel +966 593 66 23 84Email seedris@kau.edu.sa; jalama@kau.edu.sa

Background: Type 2 diabetes, or T2D, is a metabolic disease that results in insulin resistance. In the present study, we hypothesize that metabolomic analysis in blood samples of T2D patients sharing the same ethnic background can recover new metabolic biomarkers and pathways that elucidate early diagnosis and predict the incidence of T2D.Methods: The study included 34 T2D patients and 33 healthy volunteers recruited between the years 2012 and 2013; the secondary metabolites were extracted from blood samples and analyzed using HPLC.Results: Principal coordinate analysis and hierarchical clustering patterns for the uncharacterized negatively and positively charged metabolites indicated that samples from healthy individuals and T2D patients were largely separated with only a few exceptions. The inspection of the top 10% secondary metabolites indicated an increase in fucose, tryptophan and choline levels in the T2D patients, while there was a reduction in carnitine, homoserine, allothreonine, serine and betaine as compared to healthy individuals. These metabolites participate mainly in three cross-talking pathways, namely glucagon signaling, glycine, serine and threonine and bile secretion. Reduced level of carnitine in T2D patients is known to participate in the impaired insulin-stimulated glucose utilization, while reduced betaine level in T2D patients is known as a common feature of this metabolic syndrome and can result in the reduced glycine production and the occurrence of insulin resistance. However, reduced levels of serine, homoserine and allothrionine, substrates for glycine production, indicate the depletion of glycine, thus possibly impair insulin sensitivity in T2D patients of the present study.Conclusion: We introduce serine, homoserine and allothrionine as new potential biomarkers of T2D.

Keywords: glucagon signaling, glycine production, bile secretion, insulin sensitivity/resistance

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License.By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.

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How to bring precision medicine into the doctor’s office – World Economic Forum

December 17th, 2019 8:42 am

Are you one of the 26 million people who have experienced genetic testing by companies such as 23andMe or Ancestry? These companies promise to reveal what your genes say about your health and ancestry. Genes are, indeed, the instruction book containing the code that makes you a unique human being. This specific code which you inherit from your parents is what makes you, you.

The genetic coding system works amazingly well, but like all systems, occasionally things dont go as planned. You may inherit a gene that increases your chance of developing a health condition and sometimes the code develops an error causing you to have a devastating disease.

If genetic testing is so powerful in analysing and understanding your health, why cant you just as easily have this same genetic information inform your care at the doctors office? To answer this question, lets first look at the field of using genetic information to drive your healthcare (often referred to as precision or personalized medicine).

Across the globe, researchers devote enormous amounts of time and effort to understand how human genes impact health and billions of dollars are invested. The knowledge of what impact specific genes have on our health has increased tremendously and continues to do so at an amazing pace. Our increased understanding of genes, and how they affect our health, is driving novel methods to halt diseases and new ways of thinking about how medications can be developed to treat diseases.

Precision medicine is a growth area

With all this money and effort being expended, why isnt the use of your genetic information a standard part of your medical care? As the Kaiser Permanente Fellow to the World Economic Forums Precision Medicine Team, I recently had the opportunity to interview leaders from every aspect of Precision Medicine to understand the barriers preventing genetic testing from becoming a standard part of your healthcare.

Those with whom I spoke included insurance companies who pay for the tests, doctors who use and interpret them, genetic counsellors who help you understand test results, diagnostic companies which develop testing, government healthcare regulators, researchers making astonishing discoveries and healthcare organizations who are determining how best to deploy genetic testing.

These interviews suggest that the science behind genetic testing and the knowledge of how genes impact health is far ahead of our ability to make full use of this information in healthcare. Moving genetic testing into your doctors office requires a complex set of technologies, processes, knowledge and payments. Though many of the barriers inhibiting this movement were unique and complex, there were some consistent and common themes:

1. The limited expertise in genetics within healthcare systems. The need for education of healthcare providers as well as the public was regularly highlighted. The use of genetics in healthcare requires specialized knowledge that is outside the expertise of most doctors. Healthcare providers simply dont have time to study this new and rapidly changing information as their hands are full just keeping up with the latest trends and findings in their specialities. Additionally, education on genetics in healthcare is needed for the public. As one person interviewed said: The public watches CSI and thinks the use of DNA and genetics is black and white; using genetics in healthcare is rarely black and white

2. The lack of sufficient genetic counsellors. Genetic counsellors are often used to engage patients prior to testing and after results have been received, providing them with the detailed and nuanced information required for many of these tests. They also support doctors when they need assistance in making decisions about genetic testing and understanding the test results.

3. To successfully embed genetics into your care, doctors need the workflows for genetic testing (receiving results and understanding the impact on their care plans) to become a seamless part of their work. Clinical decision support software for genetics should alert the healthcare provider when genetic testing is merited with a patient, based on information the provider has entered during their examination. The software should then provide a list of appropriate tests and an explanation of why one might be used over another. After doctors order the test, they believe is most appropriate, the system should inform them of the results in clear, easily understandable language. The results should inform the doctor if the care plan for this patient should be modified (with suggestions for how the care should change).

4. Coverage of payments for genetic testing. If such tests are not paid for by insurers or government healthcare agencies (the payers), doctors simply wont order them. In the US and many other countries, there is patchwork coverage for genetic testing. Some tests are covered under specific circumstances, but many are not covered at all. The major reason cited by the payers for not covering genetic testing is a lack of evidence of clinical efficacy. In other words, do these tests provide actionable information, that your doctor can use to ensure better health outcomes? Until the payers see sufficient evidence of clinical efficacy, they will be hesitant to pay for many types of genetic testing. Doctors are concerned about the same thing, according to my research. They want to see the use of these tests in large populations, so they can determine that there is a benefit to using them.

Using your genetic information in healthcare is much more complex than taking a direct-to-consumer genetic test such as those offered by 23andMe. Healthcare is a multifaceted system and doctors already have too much on their plate. As such, there must be sufficient proof that the use of genetic testing will result in better health outcomes for the populations these clinicians serve before it's introduced into this setting.

We cannot hesitate in the face of the above complexities. As I completed the interviews which revealed these barriers, I stumbled across a journal article on this very subject. Written by a prominent group of doctors and researchers from government and leading universities in 2013, it highlights these same barriers and that virtually no progress has been made in the ensuing seven years. This is why I am focusing my fellowship at the World Economic Forum on a new project called Moving Genomics to the Clinic. Taking advantage of the multistakeholder platform of the Forum, the project will quicken the pace of tackling these barriers so that the use of genetic information can become a standard part of your healthcare experience.

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Arthur Hermann, Fellow, Precision Medicine, World Economic Forum

The views expressed in this article are those of the author alone and not the World Economic Forum.

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Myriad’s Polygenic Risk Score Personalizes Risk of Breast Cancer for Woman with a Genetic Mutation in Important Breast Cancer GenesNew Clinical…

December 17th, 2019 8:42 am

SALT LAKE CITY, Dec. 14, 2019 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in molecular diagnostics and precision medicine, announced that results of a new validation study of the companys polygenic risk score (PRS) for breast cancer were presented at the 2019 San Antonio Breast Cancer Symposium (SABCS) in San Antonio, Tx. The key finding is that the PRS significantly improves the precision and accuracy of breast cancer risk estimates for women of European ancestry who have pathogenic variants (PV) in high- and moderate-penetrance breast cancer genes.

Our goal is to help women understand their risk of breast cancer so that they can take steps to live longer, healthier lives. Women who have a family history of breast cancer should consider hereditary cancer testing with the myRisk Hereditary Cancer test, said Jerry Lanchbury, Ph.D., chief scientific officer of Myriad Genetics. In this landmark study, we demonstrated that for women who test positive for a mutation in one of the five most common breast cancer genes, there are additional genetic factors called single nucleotide polymorphisms (SNPs) that can further influence their lifetime risk of breast cancer.

A summary of the study follows below. Follow Myriad on Twitter via @myriadgenetics and keep up to date with SABCS meeting news and updates by using the #SACBS19 hashtag.

Myriad Poster Presentation Title: Polygenic Breast Cancer Risk Modification in Carriers of High and Intermediate Risk Gene Mutations.Presenter: Elisha Hughes, Ph.D.Date: Saturday, Dec. 14, 2019, 7:009:00 a.m.Location: Poster P6-08-07

This validation study evaluated the 86-SNP PRS as a breast cancer risk factor for women who carry PV in the BRCA1, BRCA2, CHEK2, ATM and PALB2 genes and for PV-free women. The analysis included data from 152,012 women of European ancestry who received a myRisk Hereditary Cancer test as part of their clinical hereditary cancer risk assessment. The results demonstrated that the 86-SNP PRS significantly modified the breast cancer risk for women with pathogenic mutations in the five tested breast cancer genes (p-value <10-4). For some women, the PRS significantly increased the gene-based risk of breast cancer, while in others the gene-based risk was reduced (see Graph 1). Importantly, the greatest PRS risk-modification was observed in carriers of CHEK2, ATM and PALB2 mutations with some women reaching the risk levels associated with BRCA1 and BRCA2 mutations.

To view Graph 1: PRS Significantly Modifies Lifetime Breast Cancer Risk in Mutation Carriers , please visit the following link: https://www.globenewswire.com/NewsRoom/AttachmentNg/d56c93ca-e00f-452d-b051-6325a578454c

These findings mean that we have the potential to significantly improve the precision of hereditary cancer risk assessment for women who test positive for mutations in the high and intermediate risk breast cancer genes, said Elisha Hughes, Ph.D., lead investigator and director of Bioinformatics at Myriad Genetics. We are optimistic that this additional genetic information can help clinicians more accurately predict the risk of breast cancer and provide the best care for their patients in the future.

Next StepsThe company plans to publish these new data in a peer reviewed medical journal and make the PRS available for U.S. women of European ancestry who test positive for mutations in breast cancer genes. The PRS currently is available as part of myRisk Hereditary Cancer enhanced with riskScore for women of European ancestry who test negative for pathogenic mutations in the breast cancer genes. Specifically, the riskScore test combines the PRS with the Tyrer-Cuzick model to estimate a womans 5-year and lifetime risk for developing breast cancer. The company is committed to making myRisk Hereditary Cancer enhanced with riskScore available to all ethnicities and is developing the test for women of Hispanic and African-American ancestry who test negative. The company is currently conducting the largest ever PRS study in African Americans and will present the data at a future meeting.

Please visit Myriad at booth #113 to learn more about our portfolio of genetic tests for breast cancer. Follow Myriad on Twitter via @myriadgenetics and keep up to date with Symposium news by using the hashtag #SABCS19.

About riskScoreriskScore is a new clinically validated personalized medicine tool that enhances Myriads myRisk Hereditary Cancer test. riskScore helps to further predict a womens lifetime risk of developing breast cancer using clinical risk factors and genetic-markers throughout the genome. The test incorporates data from more than 80 single nucleotide polymorphisms identified through 20 years of genome wide association studies in breast cancer and was validated in our laboratory to predict breast cancer risk in women of European descent. This data is then combined with a best-in-class family and personal history algorithm, the Tyrer-Cuzick model, to provide every patient with individualized breast cancer risk.

About Myriad myRisk Hereditary CancerThe Myriad myRisk Hereditary Cancer test uses an extensive number of sophisticated technologies and proprietary algorithms to evaluate 35 clinically significant genes associated with eight hereditary cancer sites including: breast, colon, ovarian, endometrial, pancreatic, prostate and gastric cancers and melanoma.

About Myriad GeneticsMyriad Genetics Inc. is a leading precision medicine company dedicated to being a trusted advisor transforming patient lives worldwide with pioneering molecular diagnostics. Myriad discovers and commercializes molecular diagnostic tests that: determine the risk of developing disease, accurately diagnose disease, assess the risk of disease progression, and guide treatment decisions across six major medical specialties where molecular diagnostics can significantly improve patient care and lower healthcare costs. Myriad is focused on five critical success factors: building upon a solid hereditary cancer foundation, growing new product volume, expanding reimbursement coverage for new products, increasing RNA kit revenue internationally and improving profitability with Elevate 2020. For more information on how Myriad is making a difference, please visit the Company's website: http://www.myriad.com.

Myriad, the Myriad logo, BART, BRACAnalysis, Colaris, Colaris AP, myPath, myRisk, Myriad myRisk, myRisk Hereditary Cancer, myChoice, myPlan, BRACAnalysis CDx, Tumor BRACAnalysis CDx, myChoice CDx, EndoPredict, Vectra, GeneSight, riskScore, Prolaris, Foresight and Prequel are trademarks or registered trademarks of Myriad Genetics, Inc. or its wholly owned subsidiaries in the United States and foreign countries. MYGN-F, MYGN-G.

Safe Harbor StatementThis press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including statements related to the Companys polygenic risk score and data being featured at the 2019 San Antonio Breast Cancer Symposium being held Dec. 10-14, 2019 in San Antonio, Tx.; the potential to significantly improve the precision of hereditary cancer risk assessment for women who test positive for mutations in the high and intermediate risk breast cancer genes; this additional genetic information helping clinicians more accurately predict the risk of breast cancer and provide the best care for their patients in the future; publishing these new data in a peer reviewed medical journal and making the PRS available for U.S. women of European ancestry who test positive for mutations in breast cancer genes; making myRisk Hereditary Cancer enhanced with riskScore available to all ethnicities and developing the test for women of Hispanic and African-American ancestry who test negative; conducting the largest ever PRS study in African Americans and presenting the data at a future meeting; and the Company's strategic directives under the caption "About Myriad Genetics." These "forward-looking statements" are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by forward-looking statements. These risks and uncertainties include, but are not limited to: the risk that sales and profit margins of our molecular diagnostic tests and pharmaceutical and clinical services may decline; risks related to our ability to transition from our existing product portfolio to our new tests, including unexpected costs and delays; risks related to decisions or changes in governmental or private insurers reimbursement levels for our tests or our ability to obtain reimbursement for our new tests at comparable levels to our existing tests; risks related to increased competition and the development of new competing tests and services; the risk that we may be unable to develop or achieve commercial success for additional molecular diagnostic tests and pharmaceutical and clinical services in a timely manner, or at all; the risk that we may not successfully develop new markets for our molecular diagnostic tests and pharmaceutical and clinical services, including our ability to successfully generate revenue outside the United States; the risk that licenses to the technology underlying our molecular diagnostic tests and pharmaceutical and clinical services and any future tests and services are terminated or cannot be maintained on satisfactory terms; risks related to delays or other problems with operating our laboratory testing facilities and our healthcare clinic; risks related to public concern over genetic testing in general or our tests in particular; risks related to regulatory requirements or enforcement in the United States and foreign countries and changes in the structure of the healthcare system or healthcare payment systems; risks related to our ability to obtain new corporate collaborations or licenses and acquire new technologies or businesses on satisfactory terms, if at all; risks related to our ability to successfully integrate and derive benefits from any technologies or businesses that we license or acquire; risks related to our projections about our business, results of operations and financial condition; risks related to the potential market opportunity for our products and services; the risk that we or our licensors may be unable to protect or that third parties will infringe the proprietary technologies underlying our tests; the risk of patent-infringement claims or challenges to the validity of our patents or other intellectual property; risks related to changes in intellectual property laws covering our molecular diagnostic tests and pharmaceutical and clinical services and patents or enforcement in the United States and foreign countries, such as the Supreme Court decision in the lawsuit brought against us by the Association for Molecular Pathology et al; risks of new, changing and competitive technologies and regulations in the United States and internationally; the risk that we may be unable to comply with financial operating covenants under our credit or lending agreements; the risk that we will be unable to pay, when due, amounts due under our credit or lending agreements; and other factors discussed under the heading "Risk Factors" contained in Item 1A of our most recent Annual Report on Form 10-K for the fiscal year ended June 30, 2019, which has been filed with the Securities and Exchange Commission, as well as any updates to those risk factors filed from time to time in our Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. All information in this press release is as of the date of the release, and Myriad undertakes no duty to update this information unless required by law.

Graph 1

PRS Significantly Modifies Lifetime Breast Cancer Risk in Mutation Carriers

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Indiana University School of Medicine researchers use cutting-edge technology to predict which triple negative breast cancer patients may avoid…

December 17th, 2019 8:42 am

IU School of Medicine 12/13/19

SAN ANTONIOIndiana University School of Medicine researchers have discovered how to predict whether triple negative breast cancer will recur,and whichwomenare likely toremain disease-free. They will present their findingson December 13, 2019,at the San Antonio Breast Cancer Symposium, the most influential gathering of breast cancer researchers and physicians in the world.

Milan Radovich, PhD, andBryan Schneider, MD,discovered that women whose plasmacontained genetic material from a tumor referred to as circulating tumor DNA had only a 56 percent chance of being cancer-free two years following chemotherapy and surgery. Patients who did not have circulating tumor DNA, or ctDNA,in their plasma had an 81 percent chance that the cancer would not return after the same amount of time.

Triple negative breast cancer is one of the most aggressive and deadliest types of breast cancer because it lacks common traits used to diagnose and treat most other breast cancers. Developing cures for the disease is a priority of theIU Precision Health Initiative Grand Challenge.

The study also examined the impact of circulating tumor cells,or CTCs,which arelive tumor cells that are released from tumors somewhere in the body and float in the blood.

What we found is that if patientswerenegative for bothctDNA and CTC, 90 percent of the women with triple negative breast cancer remained cancer-free after two years, said Radovich, who is lead author of this study and associate professor of surgery and medicalandmolecular genetics at IU School of Medicine.

Advocates for breast cancer researchsaythey are excited to hear about these results.

The implications of this discovery will change the lives of thousands of breast cancer patients, saidNadia E.Miller,who is a breast cancer survivor andpresident of Pink-4-Ever, which is a breast cancer advocacy group in Indianapolis. This is a huge leap toward more favorable outcomes and interventions for triple negative breast cancer patients. To provide physicians with more information to improve the lives of somany is encouraging!

Radovich and Schneider are researchers in theIndiana University Melvin and Bren Simon Cancer Centerand theVera Bradley Foundation Center for Breast Cancer Research. They lead the Precision Health Initiatives triple negative breast cancer team.

The researchers, along with colleagues from theHoosier Cancer Research Network, analyzed plasma samples taken from the blood of 142 women with triple negative breast cancer who had undergone chemotherapy prior to surgery. Utilizing theFoundationOne Liquid Test, circulating tumor DNA was identified in 90 of the women;52 were negative.

The women were participants inBRE12-158,a clinical study that testedgenomically directed therapyversus treatment of the physicians choicein patients withstageI,II or IIItriple negative breast cancer.

Detection of circulatingtumorDNA was also associated with poor overall survival. Specifically, the study showed that patients withcirculatingtumorDNA were four times more likely to die from the disease when compared to those who tested negative for it.

The authors say the next step is a new clinical study expected to begin in early 2020, which utilizes this discovery to enroll patients who are at high risk for recurrence and evaluates new treatment options for them.

Just telling a patient they are at high risk for reoccurrence isnt overly helpful unless you can act on it, said Schneider, who is senior author of this study and Vera Bradley Professor of Oncologyat IU School of Medicine. Whats more important is the ability to act on that in a way to improve outcomes.

Organizers of theSan Antonio Breast Cancer Symposiumselected the researchto highlight frommore than2,000 scientific submissions.

This study was funded by the Vera Bradley Foundation for Breast Cancerand the Walther Cancer Foundation.It is part of theIndiana University Precision Health InitiativeGrand Challenge.The study was managed by the Hoosier Cancer Research Network and enrolled at 22clinical sites across theUnited States.

To interviewMilan Radovich or Bryan P. Schneideron Friday, Dec. 13,contactChristine Drury at 317-385-9227 (cell)on-site in San Antonio.

Local mediacancontact Anna Carrera in Indianapolisat 614-570-6503 (cell).

For the full media kit, click here.

# # #

What theyre saying:

IU School of Medicine DeanJayL.Hess, MD, PhD, MHSA:While we have made extraordinary progress in treating many types of breast cancer, triple negative disease remains a formidable challenge. We are dedicating substantial expertise and resources to this disease, and this discovery is an important step forward. We will continue to press ahead until we have new therapies to offer women with this most aggressive form of breast cancer.

IU School of Medicine Executive Associate Dean for ResearchAnanthaShekhar, MD, PhD:I could not be more proud of our research team here at IU School of Medicine and the IU Precision Health InitiativeGrand Challenge. A few years ago, I gave the teams the challenge to come up with targeted treatments, cures and preventions for triple negative breast cancer, where there had been none. The findings, announced today, show we are well on our way to achieving these bold goals.

Indiana University Melvin and Bren Simon Cancer Center DirectorPatrick J. Loehrer, MD:Addressing an issue of importance in Indiana and globally, our IU cancer researchers are making novel discoveries that have the real potential to impact women with triple negative breast cancer. This work does not happen in a vacuum, but is a product of team science, which characterizes the fabric of our National Cancer Institute-designated Comprehensive Cancer Center.

###

IU School of Medicine is the largest medical school in the U.S. and is annually ranked among the top medical schools in the nation by U.S. News & World Report. The school offers high-quality medical education, access to leading medical research and rich campus life in nine Indiana cities, including rural and urban locations consistently recognized for livability.

The Precision Health Initiative is IUs big health care solution. Led by the IU School of Medicine, the Precision Health Initiative team is working to prevent and cure diseases through a more precise understanding of the genetic, behavioral, and environmental factors that influence a persons health, with bold goals to cure one cancer and one childhood disease and to prevent one chronic illness and one neurodegenerative disease.

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This genetic variant is underdiagnosed, under-recognized, and deadly | Penn Today – Penn: Office of University Communications

December 17th, 2019 8:42 am

A genetic variant in the gene transthyretin (TTR)which is found in about 3 percent of individuals of African ancestryis a more significant cause of heart failure than previously believed, according to a multi-institution study led by researchers atPenn Medicine. The study also revealed that a disease caused by this genetic variant, called hereditary transthyretin amyloid cardiomyopathy (hATTR-CM), is significantly under-recognized and underdiagnosed.

The findings, which were published inJAMA, are particularly important given the U.S. Food and Drug Administrations approvalof the first therapy (tafamidis) for ATTR-CM in May 2019. Prior to the new therapy, treatment was largely limited to supportive care for heart failure symptoms and, in rare cases, heart transplant.

Our findings suggest that hATTR-CM is a more common cause of heart failure than its perceived to be, and that physicians are not sufficiently considering the diagnosis in certain patients who present with heart failure, says the studys corresponding authorDaniel J. Rader, chair of the Department of Genetics at Penn Medicine. With the recent advances in treatment, its critical to identify patients at risk for the disease and, when appropriate, perform the necessary testing to produce an earlier diagnosis and make the effective therapy available.

Read more at Penn Medicine News.

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Triplet Therapeutics Launches with $59 Million in Financing to Further its Development of Transformative Treatments for Triplet Repeat Disorders -…

December 17th, 2019 8:42 am

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Triplet Therapeutics, Inc., a biotechnology company harnessing human genetics to develop treatments for repeat expansion disorders at their source, launched today with $59 million in financing including a $49 million Series A financing led by MPM Capital and Pfizer Ventures U.S. LLC, the venture capital arm of Pfizer Inc. (NYSE: PFE). Atlas Venture, which co-founded and seeded Triplet with a $10 million investment, also participated in the Series A alongside Invus, Partners Innovation Fund and Alexandria Venture Investments.

Triplet was founded in 2018 by Nessan Bermingham, Ph.D., a serial biotech entrepreneur and venture partner at Atlas Venture, along with Atlas Venture and Andrew Fraley, Ph.D., to pursue a transformative approach to developing treatments for repeat expansion disorders, a group of more than 40 known genetic diseases associated with expanded DNA nucleotide repeats. A significant body of human genetic evidence has identified that one central pathway, known as the DNA damage response (DDR) pathway, drives onset and progression of this group of disorders, which include Huntingtons disease, myotonic dystrophy and various spinocerebellar ataxias.

Triplet is developing antisense oligonucleotide (ASO) and small interfering RNA (siRNA) development candidates to precisely knock down key components of the DDR pathway that drive repeat expansion. This approach operates upstream of current approaches in development, targeting the fundamental driver of these diseases. By precisely reducing activity of select DDR targets, Triplets approach is designed to halt onset and progression across a wide range of repeat expansion disorders.

The company has a fully assembled senior management team of industry veterans. Nessan Bermingham, Ph.D., co-founder, president and chief executive officer, has nearly two decades of experience leading life science startups and is a co-founder of Intellia Therapeutics and Korro Bio. Irina Antonijevic, M.D., Ph.D., senior vice president of development, previously led translational medicine and early development at Wave Life Sciences. Brian Bettencourt, Ph.D., senior vice president of computational biology & statistics, comes to Triplet from Translate Bio, where he led modeling and design of oligonucleotide and mRNA therapeutics. David Morrissey, Ph.D., senior vice president of technology, formerly led technology development and delivery of CRISPR/Cas9 gene editing candidates at Intellia Therapeutics. Eric Sullivan, CPA, chief financial officer, brings experience leading financial operations at Gemini Therapeutics and bluebird bio. Jeffrey M. Cerio, Pharm.D., J.D., senior vice president & general counsel, served as senior corporate counsel at Moderna, Inc. before joining the Triplet team.

Were excited to launch Triplet today to transform the treatment of repeat expansion disorders, Dr. Bermingham said. This milestone would not have been possible without the contributions of thousands of patients, whose participation in genetic research has enabled us to build a fundamentally new understanding of the cause of these diseases. With this financing we are positioned to rapidly advance our initial development candidates toward the clinic for patients.

The company will use the Series A funds to progress its first development candidates into IND-enabling studies, as well as to advance natural history studies to inform its clinical development plan and contribute to the scientific understanding of repeat expansion disorders.

More than 40 repeat expansion disorders have been identified, and most of these diseases are severe with limited to no treatment options, said Jean-Franois Formela, M.D., partner at Atlas Venture and Board Chair of Triplet. We have built Triplet to fundamentally transform what has been the treatment strategy for these diseases up to now.

The companys founding Board of Directors is comprised of:

Triplets launch today represents a turning point for the treatment of repeat expansion disorders. I look forward to working with this expert team to develop novel treatments for patients, said Shinichiro Fuse, Ph.D., partner at MPM Capital and member of Triplets Board of Directors.

This group of severe genetic disorders represents an area of high unmet medical need, and we look forward to working with Triplets leadership team as they reimagine the potential treatment paradigm for patients with rare diseases, said Laszlo Kiss, Ph.D., Pfizer Ventures principal and member of Triplets Board of Directors.

Triplet has also formed a Scientific Advisory Board comprised of leading investigators for repeat expansion disorders, including Sarah Tabrizi, Ph.D., professor of clinical neurology at University College London; Jim Gusella, Ph.D., Bullard Professor of Neurogenetics at Harvard Medical School; and Vanessa Wheeler, Ph.D., associate professor of neurology at Massachusetts General Hospital and Harvard Medical School.

About Triplet Therapeutics

Triplet Therapeutics is a biotechnology company developing transformational treatments for patients with unmet medical needs by leveraging insights of human genetics to target the underlying cause of repeat expansion disorders, a group of more than 40 known genetic diseases including Huntingtons disease, myotonic dystrophy and spinocerebellar ataxias. Triplet was founded by Nessan Bermingham, Ph.D., Atlas Venture and Andrew Fraley, Ph.D. Triplet has raised $59 million in funding to date, including its Series A funding in 2019 led by MPM Capital and Pfizer Ventures, with Atlas Venture, Invus, Partners Innovation Fund and Alexandria Venture Investments participating. Triplet is headquartered in Cambridge, Mass. For more information, please visit http://www.triplettx.com.

About Atlas Venture

Atlas Venture is a leading biotech venture capital firm. With the goal of doing well by doing good, we have been building breakthrough biotech startups for over 25 years. We work side by side with exceptional scientists and entrepreneurs to translate high impact science into medicines for patients. Our seed-led venture creation strategy rigorously selects and focuses investment on the most compelling opportunities to build scalable businesses and realize value. For more information, please visit http://www.atlasventure.com.

About MPM Capital

MPM Capital is a healthcare investment firm founding and investing in life sciences companies that seek to cure major diseases by translating scientific innovations into positive clinical outcomes. MPM invests in breakthrough therapeutics, with a focus on oncology. With its experienced and dedicated team of investment professionals, executive partners, entrepreneurs and scientific advisory board members, MPM is powering novel medical breakthroughs that transform patients lives. http://www.mpmcapital.com

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