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DNA Sequencing Industry Outlook 2020-2025 – Increasing Application in Clinical Diagnosis & Drug Discovery is Driving Growth -…

August 15th, 2020 9:49 am

DUBLIN--(BUSINESS WIRE)--The "Global DNA Sequencing Market: Growth, Trends & Forecast 2020-2025" report has been added to ResearchAndMarkets.com's offering.

The Global DNA Sequencing Market is expected to witness a CAGR of 18.9% during the forecast period.

Certain factors that are driving the market growth include the rise in technological advancements in DNA sequencing, increasing application in clinical diagnosis & drug discovery, and growing investment in R&D.

The technological advancements in sequencing, from 2D sequencing in the 1970's to DNA sequencing, has come a long way. In the recent years, platforms, such as Illumina/ Solexa, ABI/ SOLiD, 454/Roche, and Helicos, have provided unique prospects for high-throughput functional genomic research. After the introduction of NGS technologies in 2005, they have had an incredible influence on genomic research.

Next-generation sequencing, currently, has its application in the diagnosis of a variety of illnesses, such as cancer, hematological disorders, neurology, psychiatry, dysmorphology, vision and hearing impairment, cardiology, and pharmacogenomics. It is also used as a tool for noninvasive prenatal tests. NGS technologies have been used for standard sequencing applications, like genome sequencing and for novel applications that were previously unexplored by using Sanger sequencing.

Applications include whole genome and transcriptome sequencing, metagenomic characterization of microbial types in environmental and clinical specimens, explanation of DNA binding sites for chromatin and regulatory proteins, and targeted re-sequencing of specific sites in the human genome, identified by linkage analyses.

Key Market Trends

Next Generation Sequencing is Expected to Show Lucrative Growth Opportunity in the Platform Segment

Next Generation Sequencing can be of several types based on the technology. For example, the benefits offered by whole genome sequencing technique, such as ease of handling, affordability, and accuracy, are expected to boost their demand. Additionally, these tests are usually preferred by the market players as a single test, which is capable of providing information on multiple factors, such as virulence, serotype, and resistance.

FDA is applying NGS in innovative ways, which can help reduce foodborne illnesses and deaths. Isolation of pathogens from food or environmental samples may be compared to clinical isolates from patients. A reliable link between the two is made, which helps define the scope of a foodborne illness outbreak. Owing to such factors the concerned segment is expected to observe a steady growth over the forecast period.

North America Dominates the Market and Expected to do Same in the Forecast Period

The North America dominated the global market studied, in 2018, owing to the increasing funding and support activities by the government and non-government entities, especially in the United States. By supporting genomics research, various government bodies, like NHGRI (National Human Genome Research Institute) have supported the work on sequencing of the human genome, and fund research on the genome's structure, function, and role in health and disease.

They also support studies on the ethical, legal, and social implications (ELSI) of genome research. The US National Human Genome Research Institute and the US National Academy of Medicine, organized 90 leaders in genomic medicine from the United States, and 25 other countries in Genomic Medicine Symposium in 2014, in order to identify opportunities for collaborations that promote the responsible practice of genomic medicine.

Competitive Landscape

The DNA Sequencing market is highly competitive and consists of a few major players. Companies like Agilent Technologies, Inc., Bio-Rad Laboratories, Inc., Danaher Corporation, Eurofins Scientific, F. Hoffmann-La Roche, Illumina, Inc., Merck KGaA, Pacific Biosciences of California, Inc., PerkinElmer Inc., Thermo Fisher Scientific, Inc., among others, hold the substantial market share in the DNA Sequencing market.

Key Topics Covered

1 INTRODUCTION

1.1 Study Deliverables

1.2 Study Assumptions

1.3 Scope of the Study

2 RESEARCH METHODOLOGY

3 EXECUTIVE SUMMARY

4 MARKET DYNAMICS

4.1 Market Overview

4.2 Market Drivers

4.2.1 Rise in Technological Advancements in DNA Sequencing

4.2.2 Increasing Application in Clinical Diagnosis & Drug Discovery

4.2.3 Growing Investment in R&D

4.3 Market Restraints

4.3.1 Interpretation of Complex Data and Lack of Skilled Professionals

4.3.2 Legal and Ethical Issues

4.4 Porter's Five Force Analysis

5 MARKET SEGMENTATION

5.1 Product Type

5.1.1 Instruments

5.1.2 Consumables (Kits, Reagents)

5.1.3 Others

5.2 Platform

5.2.1 Sanger

5.2.2 Next Generation Sequencing

5.2.3 qPCR

5.2.4 Others

5.3 Application

5.3.1 Diagnostics

5.3.2 Personalized Medicine

5.3.3 Others (Biomarkers, Forensics, Reproductive Health etc.)

5.4 End User

5.4.1 Hospitals and Healthcare Organizations

5.4.2 Academics and Research Institutions

5.4.3 Pharmaceutical and Biotechnology Companies

5.4.4 Others

5.5 Geography

5.5.1 North America

5.5.2 Europe

5.5.3 Asia Pacific

5.5.4 Middle East and Africa

5.5.5 South America

6 COMPETITIVE LANDSCAPE

6.1 Company Profiles

6.1.1 Agilent Technologies, Inc.

6.1.2 Bio-Rad Laboratories, Inc.

6.1.3 Danaher Corporation (Beckman Coulter, Inc.)

6.1.4 Eurofins Scientific

6.1.5 F. Hoffmann-La Roche

6.1.6 Illumina, Inc.

6.1.7 Merck KGaA

6.1.8 Pacific Biosciences of California, Inc.

6.1.9 PerkinElmer Inc.

6.1.10 Thermo Fisher Scientific, Inc.

7 MARKET OPPORTUNITIES AND FUTURE TRENDS

For more information about this report visit https://www.researchandmarkets.com/r/29pmu9

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New AI-Based Software Precisely Assesses Progression of Retinal Legions from Geographic Atrophy – AZoRobotics

August 15th, 2020 9:49 am

Written by AZoRoboticsAug 14 2020

Researchers from the Eye Clinic of the University Hospital Bonn, Stanford University, and the University of Utah have developed an artificial intelligence (AI)-based software that enables the accurate evaluation of the progression of geographic atrophy (GA).

Geographic atrophy is a disease of the light-sensitive retina that occurs due to age-related macular degeneration (AMD).

This novel technique enables fully automated measurement of the main atrophic lesions with the help of data obtained from optical coherence tomography, which offers three-dimensional visualization of the retinas structure.

Moreover, the researchers can accurately identify the integrity of light-sensitive cells of the whole central retina, as well as detect progressive degenerative variations of what are called the photoreceptors beyond the main lesions.

The study results will be used to evaluate the effectiveness of new innovative therapeutic approaches. The study was published recently in the JAMA Ophthalmology journal.

Currently, there exists no viable treatment for geographic atrophy, which is one of the most common reasons for blindness in industrialized nations. The disease impairs the cells of the retina and destroys them.

The main lesions, regions of the degenerated retina, also called geographic atrophy, tend to expand with the progression of the disease and lead to blind spots in the visual field of the patient. A main difficulty faced in the case of assessment therapies is that the lesions tend to progress gradually, implying that a long follow-up period is required for intervention studies.

When evaluating therapeutic approaches, we have so far concentrated primarily on the main lesions of the disease. However, in addition to central visual field loss, patients also suffer from symptoms such as a reduced light sensitivity in the surrounding retina.

Dr Frank G. Holz, Professor and Director, Eye Clinic, University Hospital Bonn.

Dr Holz added, Preserving the microstructure of the retina outside the main lesions would therefore already be an important achievement, which could be used to verify the effectiveness of future therapeutic approaches.

Moreover, the researchers could demonstrate that the integrity of light-sensitive cells exterior to the geographic atrophy areas is a predictor of the future progression of the disease.

It may therefore be possible to slow down the progression of the main atrophic lesions by using therapeutic approaches that protect the surrounding light sensitive cells.

Monika Fleckenstein, Professor, Moran Eye Center, University of Utah

Prof. Fleckenstein is the initiator of the Bonn-based natural history study on geographic atrophy, based on which this study was performed.

Research in ophthalmology is increasingly data-driven. The fully automated, precise analysis of the finest, microstructural changes in optical coherence tomography data using AI represents an important step towards personalized medicine for patients with age-related macular degeneration.

Dr Maximilian Pfau, Study Lead Author, Eye Clinic, University Hospital Bonn

Dr Pfau, who is currently a fellow of the German Research Foundation (DFG) and postdoctoral fellow at Stanford University in the Department of Biomedical Data Science, added that It would also be useful to re-evaluate older treatment studies with the new methods in order to assess possible effects on photoreceptor integrity.

Pfau, M., et al. (2020) Progression of Photoreceptor Degeneration in Geographic Atrophy Secondary to Age-related Macular Degeneration. JAMA Ophthalmology. doi.org/10.1001/jamaophthalmol.2020.2914.

Source: https://www.uni-bonn.de/en?set_language=en

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Healthcare Descriptive Analysis Industry 2020-2025: Financial Data Analytics Expected to Dominate Over the Forecast Period – ResearchAndMarkets.com -…

August 15th, 2020 9:49 am

The "Healthcare Descriptive Analysis Market: Growth, Trends and Forecasts (2020-2025)" report has been added to ResearchAndMarkets.com's offering.

Increasing need to reduce healthcare expenditure, including cost associated with medical product flaws and hospital workflow inefficiencies, is anticipated to increase the usage of big data in the healthcare sector.

The digitalization of healthcare data is also one of the primary drivers of healthcare analytics. According to Intel, approximately more than 80% of the healthcare organizations in the U.S. have adopted Electronic Medical Records (EMR) systems. These systems collect a lot of data, which can be analyzed using various types of healthcare analytics to develop personalized medicine.

Advanced methods such as predictive analytics are widely used in government organizations such as healthcare financing systems primarily to avoid frauds in payments. For instance, in 2011, the Centers of Medicare and Medicaid Services (CMS) reported that under its Fraud Prevention System (FPS), predictive analytics helped in saving USD 1.5 billion through improper payments. Moreover, the CMS is developing next generation predictive analytics, which is expected to boost the usage of predictive analytics.

Key Market Trends

Financial Data Analytics Segment Expected to Dominate the Market Over the Forecast Years

By application, the market has been segmented into clinical, financial, administrative, and research data analytics. The Financial Data Analytics segment is expected to register significant growth during the forecast period due to the technologically advanced solutions by healthcare providers and increased focus of payers on the early detection of fraud and reducing preventable costs.

North America Expected to Dominate the World Market

North America is expected to dominate the market followed by Europe. Factors, such as growing federal healthcare mandates to curb rising healthcare costs and provide quality care; increasing regulatory requirements; growing EHR adoption; and rising government initiatives focusing on personalized medicine, population health management, and value-based reimbursements are expected to drive market growth in North America.

Competitive Landscape

The Healthcare Descriptive Analysis market is moderately competitive and many of the global players are into the market. For instance - IBM, Inovalon, Cerner Corporation, Oracle Corporation, McKesson Corporation, MedeAnalytics, Inc., Optum, Inc., Allscripts Healthcare Solutions, Inc., etc. are providing healthcare descriptive analysis products across the globe.

Key Topics Covered

1 INTRODUCTION

1.1 Study Deliverables

1.2 Study Assumptions

1.3 Scope of the Study

2 RESEARCH METHODOLOGY

3 EXECUTIVE SUMMARY

4 MARKET DYNAMICS

4.1 Market Overview

4.2 Market Drivers

4.2.1 Need for Comprehensive Analytics

4.2.2 Integration of Big Data into Healthcare

4.3 Market Restraints

4.3.1 Data Privacy and Security Concerns

4.3.2 High Costs of Initial Investment

4.4 Porter's Five Force Analysis

5 MARKET SEGMENTATION

5.1 By Application

5.1.1 Clinical Data Analytics

5.1.2 Financial Data Analytics

5.1.3 Administrative Data Analytics

5.1.4 Research Data Analytics

5.2 By Component

5.2.1 Software

5.2.2 Hardware

5.2.3 Services

5.3 By Deployment

5.3.1 On-Premise

5.3.2 Web-based

5.3.3 Cloud based

5.4 By End-user

5.4.1 Private organization

5.4.1.1 Hospitals

5.4.1.2 Physicians

5.4.1.3 Clinics

5.4.1.4 Others

5.5 Geography

5.5.1 North America

5.5.1.1 United States

5.5.1.2 Canada

5.5.1.3 Mexico

5.5.2 Europe

5.5.2.1 Germany

5.5.2.2 UK

5.5.2.3 France

5.5.2.4 Italy

5.5.2.5 Spain

5.5.2.6 Rest of Europe

5.5.3 Asia-Pacific

5.5.3.1 China

5.5.3.2 Japan

5.5.3.3 India

5.5.3.4 Australia

5.5.3.5 South Korea

5.5.3.6 Rest of Asia-Pacific

5.5.4 Middle-East and Africa

5.5.4.1 GCC

5.5.4.2 South Africa

5.5.4.3 Rest of Middle-East and Africa

5.5.5 South America

5.5.5.1 Brazil

5.5.5.2 Argentina

5.5.5.3 Rest of South America

6 COMPETITIVE LANDSCAPE

6.1 Company Profiles

6.1.1 IBM

6.1.2 Allscripts Healthcare Solutions, Inc.

6.1.3 Cerner Corporation

6.1.4 Inovalon

6.1.5 McKesson Corporation

6.1.6 MedeAnalytics, Inc.

6.1.7 Optum

6.1.8 Oracle Corporation

7 MARKET OPPORTUNITIES AND FUTURE TRENDS

For more information about this report visit https://www.researchandmarkets.com/r/iflgkx

View source version on businesswire.com: https://www.businesswire.com/news/home/20200811005670/en/

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Outlook on the Worldwide Biomarkers Industry to 2025 Scientect – Scientect

August 15th, 2020 9:49 am

The Biomarkers market report provides a detailed analysis of global market size, regional and country-level market size, segmentation market growth, market share, competitive Landscape, sales analysis, impact of domestic and global market players, value chain optimization, trade regulations, recent developments, opportunities analysis, strategic market growth analysis, product launches, area marketplace expanding, and technological innovations.

Our analysts monitoring the situation around the Globe explain that after COVID-19 crisis the market will generate remunerative prospects for producers. The goal of the report is to provide a further illustration of the current scenario, economic slowdown and effect of COVID-19 on the industry as a whole.

Biomarkers Market was valued at USD 36.3 Billion in 2018 and expected to reach USD 91.4 Billion by 2025 with a CAGR of 14.1% during the forecast period. Increasing prevalence of cancer and growing precision medicine market are amongst the pivotal factors anticipated to spur the growth of Biomarkers Market.

The global biomarkers market is witnessing a healthy growth trajectory attributed to the growing application of biomarkers in diagnostics, increasing funding for biomarkers research, as well as its rising usage in drug discovery. Biomarkers are biological molecules found in body fluids and tissues that help in crucial clinical decision making and diagnosing various health conditions of the patients. Since the molecules can analyze pharmacological responses and pathological indications, they can effectively assist in process of drug discovery and development.

The diagnostics industry has been witnessing a shift in trend from using conventional diagnostic tools towards using more advanced diagnostic methods that focus on producing accurate and consistent results during early stage of diseases. This has led to boost in demand for biomarkers which are minimally or non-invasive tools to detect diseases such as cancer at early stage. Moreover, growing usage of precision medicine should further boost the biomarkers market growth.

Apart from this, expediting growth in the healthcare IT industry and low costs of clinical trials in emerging countries has favored the entry of various new players in the market. A large chunk of funding is being invested in research and development for new product launches. For instance, in March 2018, Genomic Health, Inc. launched the Oncotype DX AR-V7 Nucleus Detect test. The AR-V7 protein is a prognostic and predictive biomarker. This test aids physicians in taking therapeutic decisions in patients suffering from metastatic castration-resistant prostate cancer (mCRPC) by accurately detecting a splice variant of the androgen receptor protein (AR-V7) in the nucleus of circulating tumor cells (CTCs).

Recent Developments In May 2019, Qiagen announced the immediate launch of its first companion diagnostics assay therascreen PIK3CA RGQ PCR Kit (therascreen PIK3CA Kit) post U.S. FDA regulatory approval as a companion diagnostic to assist in diagnosing breast cancer patients that would be eligible for treatment with newly approved therapy PIQRAY (alpelisib) developed and marketed by Novartis.

Key Players in Biomarkers Market Some of the major players operating in the Global Biomarkers Market include Siemens Healthineers, Medtronic, F. Hoffman LA Roche Ltd., Abbott Laboratories Nexus-DX, Qiagen N.V., PerkinElmer, Inc., Lifesign LLC., Merck & Co, Inc., Bio-Rad Laboratories, EKF Diagnostics Holdings plc, Singulex, Inc., Signosis, Inc, and BioSims Technologies among others.

Global Biomarkers market is segmented on the basis of product, type, application, and disease indication. The Global Biomarkers Market by product includes consumables, services, and software, while based on type the industry is segmented into safety, efficacy, and validation. By application market segmentation includes diagnostics, drug development, personalized medicine, and disease risk assessment. Biomarkers market by disease indication comprises of cancer, cardiovascular diseases, neurological diseases, immunological diseases, and others.

Increasing incidence of cancer and growing precision medicine market are some of the pivotal factors boosting the Biomarkers market growth. Increasing incidence of cancer is one of the pivotal factors which is set to drive the growth of Biomarkers Market. According to World Health Organization (WHO) statistics, various types of cancer accounted for more than 9.5 million deaths in 2018 worldwide. Cancer biomarkers are released by cancer causing tumors that can be detected in blood stream and other tissues, thus helping in early clinical evaluation and deciding the course of treatment.

Moreover, the World Health Assembly has passed the resolution in 2017 for Cancer Prevention and Control. This integrated approach (WHA70.12) has recommended the governments and WHO to speed up action plans specified in the Global Action Plan and 2030 UN Agenda for Sustainable Development to reduce premature mortality from cancer. This has led to a boost in demand for early cancer screening tests and procedures. Increasing focus of research institutes to develop such biomarkers is likely to spur the global Biomarkers Market growth.

Geographically, this report split global into several key Regions, revenue (Million USD) The geography (North America, Europe, Asia-Pacific, Latin America and Middle East & Africa) focusing on key countries in each region. It also covers market drivers, restraints, opportunities, challenges, and key issues in Global Biomarkers Market.

Key Benefits for Biomarkers Market Reports Global market report covers in-depth historical and forecast analysis. Global market research report provides detail information about Market Introduction, Market Summary, Global market Revenue (Revenue USD), Market Drivers, Market Restraints, Market Opportunities, Competitive Analysis, Regional and Country Level. Global market report helps to identify opportunities in market place. Global market report covers extensive analysis of emerging trends and competitive landscape.

By Product:ConsumablesServicesSoftware

By Type: SafetyEfficacyValidation

By Application:DiagnosticsDrug DevelopmentPersonalized MedicineDisease Risk Assessment

By Disease Indication:CancerCardiovascular DiseasesNeurological DiseasesImmunological DiseasesOthers

By Region North Americao U.S.o Canadao Mexico Europeo UKo Franceo Germanyo Russiao Rest of Europe Asia-Pacifico Chinao South Koreao Indiao Japano Rest of Asia-Pacific LAMEAo Latin Americao Middle Easto Africa

North America grabbed the largest share in Biomarkers Market globally In 2018, North America accounted for the largest share in the global biomarkers market owing to increasing adoption of precision medicine and rising prevalence of cancer in the region. The largest share of the region is also attributed to the rise in number of cancer cases in the U.S. and launch of Precision Medicine Initiative (PMI) by the U.S. government in 2015. According to the National Cancer Institute statistics, more than 16.5 million cases of cancer were diagnosed in 2016 in the U.S, and this number is expected to reach to 19 million in 2024.

The increasing application of biomarkers in the field of precision medicine should also drive the market in this region. Identification of biomarkers is essential for the development of precision medicine. The U.S. precision medicine industry has been booming post the launch of Precision Medicine Initiative by the government in 2015. The initiative aimed at improving the treatment outcome by offering tailor made therapies to patients. This has spurred the development of novel treatments and drugs based on an individuals genetic profile and characteristics of tumor. The Asia Pacific Biomarkers market is set to showcase lucrative growth in the coming years due to vast patient pool, increasing awareness regarding early disease detection and rising healthcare expenditure in the emerging countries of India and China.

Biomarkers Market Key Players: Siemens Healthineers Medtronic F. Hoffman LA Roche Ltd. Abbott Laboratories Nexus-DX Qiagen N.V. PerkinElmer, Inc. Lifesign LLC. Merck & Co, Inc. Bio-Rad Laboratories EKF Diagnostics Holdings plc Others

This comprehensive report will provide: Enhance your strategic decision making Assist with your research, presentations and business plans Show which emerging market opportunities to focus on Increase your industry knowledge Keep you up-to-date with crucial market developments Allow you to develop informed growth strategies Build your technical insight Illustrate trends to exploit Strengthen your analysis of competitors Provide risk analysis, helping you avoid the pitfalls other companies could make Ultimately, help you to maximize profitability for your company.

Our Market Research Solution Provides You Answer to Below Mentioned Question: Which are the driving factors responsible for the growth of market? Which are the roadblock factors of this market? What are the new opportunities, by which market will grow in coming years? What are the trends of this market? Which are main factors responsible for new product launch? How big is the global & regional market in terms of revenue, sales and production? How far will the market grow in forecast period in terms of revenue, sales and production? Which region is dominating the global market and what are the market shares of each region in the overall market in 2017? How will each segment grow over the forecast period and how much revenue will these segment account for in 2025? Which region has more opportunities?

Table of Content1 Study Coverage1.1 Biomarkers Product1.2 Key Market Segments in This Study1.3 Key Manufacturers Covered1.4 Market by Type1.5 Market by Application1.6 Study Objectives1.7 Years Considered

2 Executive Summary2.1 Global Biomarkers Market Size2.1.1 Global Biomarkers Revenue 2014-20252.1.2 Global Biomarkers Production 2014-20252.2 Biomarkers Growth Rate (CAGR) 2020-20252.3 Analysis of Competitive Landscape2.3.1 Manufacturers Market Concentration Ratio2.3.2 Key Biomarkers Manufacturers2.3.2.1 Biomarkers Manufacturing Base Distribution, Headquarters2.3.2.2 Manufacturers Biomarkers Product Offered2.3.2.3 Date of Manufacturers Enter into Biomarkers Market2.4 Key Trends for Biomarkers Markets & Products

3 Market Size by Manufacturers3.1 Biomarkers Production by Manufacturers3.1.1 Biomarkers Production by Manufacturers3.1.2 Biomarkers Production Market Share by Manufacturers3.2 Biomarkers Revenue by Manufacturers3.2.1 Biomarkers Revenue by Manufacturers (2014-2020)3.2.2 Biomarkers Revenue Share by Manufacturers (2014-2020)3.3 Biomarkers Price by Manufacturers3.4 Mergers & Acquisitions, Expansion Plans

4 Biomarkers Production by Regions4.1 Global Biomarkers Production by Regions4.1.1 Global Biomarkers Production Market Share by Regions4.1.2 Global Biomarkers Revenue Market Share by Regions4.2 North America4.2.1 North America Biomarkers Production4.2.2 North America Biomarkers Revenue4.2.3 Key Players in North America4.2.4 North America Biomarkers Import & Export4.3 Europe4.3.1 Europe Biomarkers Production4.3.2 Europe Biomarkers Revenue4.3.3 Key Players in Europe4.3.4 Europe Biomarkers Import & Export4.4 China4.4.1 China Biomarkers Production4.4.2 China Biomarkers Revenue4.4.3 Key Players in China4.4.4 China Biomarkers Import & Export4.5 Japan4.5.1 Japan Biomarkers Production4.5.2 Japan Biomarkers Revenue4.5.3 Key Players in Japan4.5.4 Japan Biomarkers Import & Export

5 Biomarkers Consumption by Regions5.1 Global Biomarkers Consumption by Regions5.1.1 Global Biomarkers Consumption by Regions5.1.2 Global Biomarkers Consumption Market Share by Regions5.2 North America5.2.1 North America Biomarkers Consumption by Application5.2.2 North America Biomarkers Consumption by Countries5.2.3 United States5.2.4 Canada5.2.5 Mexico5.3 Europe5.3.1 Europe Biomarkers Consumption by Application5.3.2 Europe Biomarkers Consumption by Countries5.3.3 Germany5.3.4 France5.3.5 UK5.3.6 Italy5.3.7 Russia5.4 Asia Pacific5.4.1 Asia Pacific Biomarkers Consumption by Application5.4.2 Asia Pacific Biomarkers Consumption by Regions5.4.3 China5.4.4 Japan5.4.5 South Korea5.4.6 India5.4.7 Australia5.4.8 Indonesia5.4.9 Thailand5.4.10 Malaysia5.4.11 Philippines

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Outlook on the Worldwide Biomarkers Industry to 2025 Scientect - Scientect

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Cellect Biotechnology Ltd ADR (NASDAQ:APOP) Receives an Approval of a Pivotal Patent for Stem Cells Activation from the European Patent Office – BP…

August 15th, 2020 9:48 am

Every successful medicinal activity requires mass production of quality stem cells. This is what avails regenerative medicine to the public the need occasioned the founding of Cellect Biotechnology Ltd ADR (NASDAQ:APOP). In 2011. The companys vision was to bring to reality regenerative treatments, which would accelerate the production of stem cell-based treatments.

Cellect has spent 15 years in research, thanks to its ApoGraft methodology, which is long-sought-after because it engages an inexpensive process. This is what has birthed seven families of patents. The company just received a pivotal patent for Stem Cells Activation from the European Patent Office. This patent, which will expire on October 7, 2034, is the most significant event for the company seeking to strengthen its Intellectual Property (IP) portfolio.

Over the past few years, the need to strengthen its IP has been a core component of the companys business strategy. According to the CEO Dr. Shai Yarkoni, they wanted to tap into the clinical and economic benefits, which come with the patent. The primary benefit and, as the company has demonstrated previously, is the increased safety and efficacy of the cell product. This is enhanced by the development of a robust and user-friendly process.

While the extensive issued patents cover the accurate elimination (negative selection) of the mature cells and therefor enables SAFETY, this patent covers the increased ACTIVITY (positive selection=efficacy) of the regenerative capacity of the stem and progenitor cells Yarkoni explained.

Cellect Biotechnology has 65 patents in nine patent families. Out of these, 45 of them have been allowed patent, 18 are waiting for examination while the remaining two are the Patent Cooperation Treaty (PCT) applications. The Biotech aim is to expand and protect global IP. This will provide researchers and clinical community tools to isolate stem cells in quantity and quality rapidly. The final results will automatically be a wide variety of applications in regenerative medicine.

Meanwhile, the company has also been consulting and discussing widely with global leaders. Before long, it will be able to take control of innovation in the development of cell therapies.

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Cellect Biotechnology Ltd ADR (NASDAQ:APOP) Receives an Approval of a Pivotal Patent for Stem Cells Activation from the European Patent Office - BP...

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Coronavirus Drug and Treatment Tracker – The New York Times

August 15th, 2020 9:48 am

The Covid-19 pandemic is one of the greatest challenges modern medicine has ever faced. Doctors and scientists are scrambling to find treatments and drugs that can save the lives of infected people and perhaps even prevent them from getting sick in the first place.

Below is an updated list of 20 of the most-talked-about treatments for the coronavirus. While some are accumulating evidence that theyre effective, most are still at early stages of research. We also included a warning about a few that are just bunk.

We are following 20 coronavirus treatments for effectiveness and safety:

Tentative or

mixed evidence

We are following 20 coronavirus treatments

for effectiveness and safety:

Tentative or

mixed evidence

We are following 20 coronavirus treatments

for effectiveness and safety:

There is no cure yet for Covid-19. And even the most promising treatments to date only help certain groups of patients and await validation from further trials. The F.D.A. has not fully licensed any treatment specifically for the coronavirus. Although it has granted emergency use authorization to some treatments, their effectiveness against Covid-19 has yet to be demonstrated in large-scale, randomized clinical trials.

This list provides a snapshot of the latest research on the coronavirus, but does not constitute medical endorsements. Always consult your doctor about treatments for Covid-19.

New additions and recent updates:

Added ivermectin, a drug typically used against parasitic worms that is being increasingly prescribed in Latin America. Aug. 10

Updated descriptions for several treatments. Aug. 10

We will update and expand the list as new evidence emerges. For details on evaluating treatments, see the N.I.H. Covid-19 Treatment Guidelines. For the current status of vaccine development, see our Coronavirus Vaccine Tracker.

WIDELY USED: These treatments have been used widely by doctors and nurses to treat patients hospitalized for diseases that affect the respiratory system, including Covid-19.

PROMISING EVIDENCE: Early evidence from studies on patients suggests effectiveness, but more research is needed. This category includes treatments that have shown improvements in morbidity, mortality and recovery in at least one randomized controlled trial, in which some people get a treatment and others get a placebo.

TENTATIVE OR MIXED EVIDENCE: Some treatments show promising results in cells or animals, which need to be confirmed in people. Others have yielded encouraging results in retrospective studies in humans, which look at existing datasets rather than starting a new trial. Some treatments have produced different results in different experiments, raising the need for larger, more rigorously designed studies to clear up the confusion.

NOT PROMISING: Early evidence suggests that these treatments do not work.

PSEUDOSCIENCE OR FRAUD: These are not treatments that researchers have ever considered using for Covid-19. Experts have warned against trying them, because they do not help against the disease and can instead be dangerous. Some people have even been arrested for their false promises of a Covid-19 cure.

EVIDENCE IN CELLS, ANIMALS or HUMANS: These labels indicate where the evidence for a treatment comes from. Researchers often start out with experiments on cells and then move onto animals. Many of those animal experiments often fail; if they dont, researchers may consider moving on to research on humans, such as retrospective studies or randomized clinical trials. In some cases, scientists are testing out treatments that were developed for other diseases, allowing them to move directly to human trials for Covid-19.

All treatmentsWidely usedPromisingTentative or mixedNot promisingPseudoscience

Antivirals can stop viruses such as H.I.V. and hepatitis C from hijacking our cells. Scientists are searching for antivirals that work against the new coronavirus.

PROMISING EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSEMERGENCY USE AUTHORIZATIONRemdesivirRemdesivir, made by Gilead Sciences, was the first drug to get emergency authorization from the F.D.A. for use on Covid-19. It stops viruses from replicating by inserting itself into new viral genes. Remdesivir was originally tested as an antiviral against Ebola and Hepatitis C, only to deliver lackluster results. But preliminary data from trials that began this spring suggested the drug can reduce the recovery time of people hospitalized with Covid-19 from 15 to 11 days. (The study defined recovery as either discharge from the hospital or hospitalization for infection-control purposes only.) These early results did not show any effect on mortality, though retrospective data released in July hints that the drug might reduce death rates among those who are very ill.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSFavipiravirOriginally designed to beat back influenza, favipiravir blocks a viruss ability to copy its genetic material. A small study in March indicated the drug might help purge the coronavirus from the airway, but results from larger, well-designed clinical trials are still pending.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSMK-4482Another antiviral originally designed to fight the flu, MK-4482 (previously known as EIDD-2801) has had promising results against the new coronavirus in studies in cells and on animals. Merck, which has been running clinical trials on the drug this summer, has announced it will launch a large Phase III trial in September.Updated Aug. 6

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS Recombinant ACE-2To enter cells, the coronavirus must first unlock them a feat it accomplishes by latching onto a human protein called ACE-2. Scientists have created artificial ACE-2 proteins which might be able to act as decoys, luring the coronavirus away from vulnerable cells. Recombinant ACE-2 proteins have shown promising results in experiments on cells, but not yet in animals or people.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS AND HUMANS IvermectinFor decades, ivermectin has served as a potent drug to treat parasitic worms. Doctors use it against river blindness and other diseases, while veterinarians give dogs a different formulation to cure heartworm. Studies on cells have suggested ivermectin might also kill viruses. But scientists have yet to find evidence in animal studies or human trials that it can treat viral diseases. As a result, Ivermectin is not approved to use as an antiviral.

In April, Australian researchers reported that the drug blocked coronaviruses in cell cultures, but they used a dosage that was so high it might have dangerous side effects in people. The FDA immediately issued a warning against taking pet medications to treat or prevent Covid-19. These animal drugs can cause serious harm in people, the agency warned.

Since then a number of clinical trials have been launched to see if a safe dose of ivermectin can fight Covid-19. In Singapore, for example, the National University Hospital is running a 5,000-person trial to see if it can prevent people from getting infected. As of now, theres no firm evidence that it works. Nevertheless ivermectin is being prescribed increasingly often in Latin America, much to the distress of disease experts.Updated Aug. 10

NOT PROMISING EVIDENCE IN CELLS AND HUMANS Lopinavir and ritonavirTwenty years ago, the F.D.A. approved this combination of drugs to treat H.I.V. Recently, researchers tried them out on the new coronavirus and found that they stopped the virus from replicating. But clinical trials in patients proved disappointing. In early July, the World Health Organization suspended trials on patients hospitalized for Covid-19. They didnt rule out studies to see if the drugs could help patients not sick enough to be hospitalized, or to prevent people exposed to the new coronavirus from falling ill. The drug could also still have a role to play in certain combination treatments.

NOT PROMISING EVIDENCE IN CELLS, ANIMALS AND HUMANSHydroxychloroquine and chloroquineGerman chemists synthesized chloroquine in the 1930s as a drug against malaria. A less toxic version, called hydroxychloroquine, was invented in 1946, and later was approved for other diseases such as lupus and rheumatoid arthritis. At the start of the Covid-19 pandemic, researchers discovered that both drugs could stop the coronavirus from replicating in cells.

Since then, theyve had a tumultuous ride. A few small studies on patients offered some hope that hydroxychloroquine could treat Covid-19. The World Health Organization launched a randomized clinical trial in March to see if it was indeed safe and effective for Covid-19, as did Novartis and a number of universities. Meanwhile, President Trump repeatedly promoted hydroxychloroquine at press conferences, touting it as a game changer, and even took it himself. The F.D.A. temporarily granted hydroxychloroquine emergency authorization for use in Covid-19 patients which a whistleblower later claimed was the result of political pressure. In the wake of the drugs newfound publicity, demand spiked, resulting in shortages for people who rely on hydroxychloroquine as a treatment for other diseases.

But more detailed studies proved disappointing. A study on monkeys found that hydroxychloroquine didnt prevent the animals from getting infected and didnt clear the virus once they got sick. Randomized clinical trials found that hydroxychloroquine didnt help people with Covid-19 get better or prevent healthy people from contracting the coronavirus. Another randomized clinical trial found that giving hydroxychloroquine to people right after being diagnosed with Covid-19 didnt reduce the severity of their disease. (One large-scale study that concluded the drug was harmful as well was later retracted.) The World Health Organization, the National Institutes of Health and Novartis have since halted trials investigating hydroxychloroquine as a treatment for Covid-19, and the F.D.A. revoked its emergency approval. The F.D.A. now warns that the drug can cause a host of serious side effects to the heart and other organs when used to treat Covid-19.

In July, researchers at Henry Ford hospital in Detroit published a study finding that hydroxychloroquine was associated with a reduction in mortality in Covid-19 patients. President Trump praised the study on Twitter, but experts raised doubts about it. The study was not a randomized controlled trial, in which some people got a placebo instead of hydroxychloroquine. The studys results might not be due to the drug killing the virus. Instead, doctors may have given the drug to people who were less sick, and thus more likely to recover anyway.

Despite negative results, a number of hydroxychloroquine trials have continued, although most are small, testing a few dozen or a few hundred patients. A recent analysis by STAT and Applied XL found more than 180 ongoing clinical trials testing hydroxychloroquine or chloroquine, for treating or preventing Covid-19. Although its clear the drugs are no panacea, its theoretically possible they could provide some benefit in combination with other treatments, or when given in early stages of the disease. Only well-designed trials can determine if thats the case.Updated Aug. 10

Most people who get Covid-19 successfully fight off the virus with a strong immune response. Drugs might help people who cant mount an adequate defense.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS AND HUMANS Convalescent plasmaA century ago, doctors filtered plasma from the blood of recovered flu patients. So-called convalescent plasma, rich with antibodies, helped people sick with flu fight their illness. Now researchers are trying out this strategy on Covid-19. In May, the F.D.A. designated convalescent plasma an investigational product. That means that despite not yet being shown as safe and effective, plasma can be used in clinical trials and given to some patients who are seriously ill with Covid-19. Tens of thousands of patients in the U.S. have received plasma through a program launched by the Mayo Clinic and the federal government.

The Trump administration has praised convalescent plasma, despite the lack of evidence yet that it works. The first wave of trials have been small and the results have been mixed. Large randomized clinical trials are underway, but theyve struggled to enroll enough participants, some of whom worry they will receive a placebo instead of the treatment itself.

Experts say that its vital to complete these trials to determine if convalescent plasma is safe and effective. If these trials are successful, it could serve as an important stopgap measure until more potent therapies become widely available.Updated Aug. 10

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSMonoclonal antibodiesConvalescent plasma from people who recover from Covid-19 contains a mix of different antibodies. Some of the molecules can attack the coronavirus, but many are directed at other pathogens. Researchers have sifted through this slurry to find the most potent antibodies against Covid-19. They have then manufactured synthetic copies of these molecules, known as monoclonal antibodies. Researchers have begun investigating them as a treatment for Covid-19, either individually or in cocktails.

Monoclonal antibodies were first developed as a therapy in the 1970s, and since then the F.D.A. has approved them for 79 diseases, ranging from cancer to AIDS. Since the start of the pandemic, researchers have found dozens of monoclonal antibodies that show promise against Covid-19 in preclinical studies on cells and animals. Companies like Eli Lilly and Regeneron recently began clinical trials studying monoclonal antibodies. Several other firms, as well as teams at universities, are slated to enter the race soon as well.Updated Aug. 10

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN CELLS, ANIMALS AND HUMANSInterferonsInterferons are molecules our cells naturally produce in response to viruses. They have profound effects on the immune system, rousing it to attack the invaders, while also reining it in to avoid damaging the bodys own tissues. Injecting synthetic interferons is now a standard treatment for a number of immune disorders. Rebif, for example, is prescribed for multiple sclerosis.

As part of its strategy to attack our bodies, the coronavirus appears to tamp down interferon. That finding has encouraged researchers to see whether a boost of interferon might help people weather Covid-19, particularly early in infection. Early studies, including experiments in cells and mice, have yielded encouraging results that have led to clinical trials.

An open-label study in China suggested that the molecules could help prevent healthy people from getting infected. On July 20, the British pharmaceutical company Synairgen announced that an inhaled form of interferon called SNG001 lowered the risk of severe Covid-19 in infected patients in a small clinical trial. The full data have not yet been released to the public, or published in a scientific journal. On August 6, the National Institute of Allergy and Infectious Diseases launched a Phase III trial on a combination of Rebif and the antiviral remdesivir, with results expected by fall 2020.Updated Aug. 10

The most severe symptoms of Covid-19 are the result of the immune systems overreaction to the virus. Scientists are testing drugs that can rein in its attack.

PROMISING EVIDENCE EVIDENCE IN HUMANS DexamethasoneThis cheap and widely available steroid blunts many types of immune responses. Doctors have long used it to treat allergies, asthma and inflammation. In June, it became the first drug shown to reduce Covid-19 deaths. That study of more than 6,000 people, which in July was published in the New England Journal of Medicine, found that dexamethasone reduced deaths by one-third in patients on ventilators, and by one-fifth in patients on oxygen. It may be less likely to help and may even harm patients who are at an earlier stage of Covid-19 infections, however. In its Covid-19 treatment guidelines, the National Institutes of Health recommends only using dexamethasone in patients with COVID-19 who are on a ventilator or are receiving supplemental oxygen.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN HUMANS Cytokine InhibitorsThe body produces signaling molecules called cytokines to fight off diseases. But manufactured in excess, cytokines can trigger the immune system to wildly overreact to infections, in a process sometimes called a cytokine storm. Researchers have created a number of drugs to halt cytokine storms, and they have proven effective against arthritis and other inflammatory disorders. Some turn off the supply of molecules that launch the production of the cytokines themselves. Others block the receptors on immune cells to which cytokines would normally bind. A few block the cellular messages they send. Depending on how the drugs are formulated, they can block one cytokine at a time, or muffle signals from several at once.

Against the coronavirus, several of these drugs have offered modest help in some trials, but faltered in others. Drug companies Regeneron and Roche drug both recently announced that two drugs called sarilumab and tocilizumab, which both target the cytokine IL-6, did not appear to benefit patients in Phase 3 clinical trials. Many other trials remain underway, several of which combine cytokine inhibitors with other treatments.Updated Aug. 10

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN HUMANS EMERGENCY USE AUTHORIZATIONBlood filtration systemsThe F.D.A. has granted emergency use authorization to several devices that filter cytokines from the blood in an attempt to cool cytokine storms. One machine, called Cytosorb, can reportedly purify a patients entire blood supply about 70 times in a 24-hour period. A small study in March suggested that Cytosorb had helped dozens of severely ill Covid-19 patients in Europe and China, but it was not a randomized clinical trial that could conclusively demonstrate it was effective. A number of studies on blood filtration systems are underway, but experts caution that these devices carry some risks. For example, such filters could remove beneficial components of blood as well, such as vitamins or medications.Updated Aug. 10

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN HUMANS Stem cellsCertain kinds of stem cells can secrete anti-inflammatory molecules. Over the years, researchers have tried to use them as a treatment for cytokine storms, and now dozens of clinical trials are under way to see if they can help patients with Covid-19. But these stem cell treatments havent worked well in the past, and its not clear yet if theyll work against the coronavirus.

Doctors and nurses often administer other supportive treatments to help patients with Covid-19.

WIDELY USEDProne positioningThe simple act of flipping Covid-19 patients onto their bellies opens up the lungs. The maneuver has become commonplace in hospitals around the world since the start of the pandemic. It might help some individuals avoid the need for ventilators entirely. The treatments benefits continue to be tested in a range of clinical trials.

WIDELY USEDEMERGENCY USE AUTHORIZATIONVentilators and other respiratory support devicesDevices that help people breathe are an essential tool in the fight against deadly respiratory illnesses. Some patients do well if they get an extra supply of oxygen through the nose or via a mask connected to an oxygen machine. Patients in severe respiratory distress may need to have a ventilator breathe for them until their lungs heal. Doctors are divided about how long to treat patients with noninvasive oxygen before deciding whether or not they need a ventilator. Not all Covid-19 patients who go on ventilators survive, but the devices are thought to be lifesaving in many cases.

TENTATIVE OR MIXED EVIDENCE EVIDENCE IN HUMANS AnticoagulantsThe coronavirus can invade cells in the lining of blood vessels, leading to tiny clots that can cause strokes and other serious harm. Anticoagulants are commonly used for other conditions, such as heart disease, to slow the formation of clots, and doctors sometimes use them on patients with Covid-19 who have clots. Many clinical trials teasing out this relationship are now underway. Some of these trials are looking at whether giving anticoagulants before any sign of clotting is beneficial.

False claims about Covid-19 cures abound. The F.D.A. maintains a list of more than 80 fraudulent Covid-19 products, and the W.H.O. debunks many myths about the disease.

WARNING: DO NOT DO THISDrinking or injecting bleach and disinfectantsIn April, President Trump suggested that disinfectants such as alcohol or bleach might be effective against the coronavirus if directly injected into the body. His comments were immediately refuted by health professionals and researchers around the world as well as the makers of Lysol and Clorox. Ingesting disinfectant would not only be ineffective against the virus, but also hazardous possibly even deadly. In July, Federal prosecutors charged four Florida men with marketing bleach as a cure for COVID-19.

WARNING: NO EVIDENCEUV lightPresident Trump also speculated about hitting the body with ultraviolet or just very powerful light. Researchers have used UV light to sterilize surfaces, including killing viruses, in carefully managed laboratories. But UV light would not be able to purge the virus from within a sick persons body. This kind of radiation can also damage the skin. Most skin cancers are a result of exposure to the UV rays naturally present in sunlight.

WARNING: NO EVIDENCESilverThe F.D.A. has threatened legal action against a host of people claiming silver-based products are safe and effective against Covid-19 including televangelist Jim Bakker and InfoWars host Alex Jones. Several metals do have natural antimicrobial properties. But products made from them have not been shown to prevent or treat the coronavirus.

Note: After additional discussions with experts we have adjusted several labels on the tracker. The Strong evidence label has been removed until further research identifies treatments that consistently benefit groups of patients infected by the coronavirus. In its place, Promising evidence will be used for drugs such as remdesivir and dexamethasone that have shown promise in at least one randomized controlled trial, and Widely used for treatments such as proning and ventilators that are often used with severely ill patients, including those with Covid-19. And we may reintroduce the Ineffective label when ongoing clinical trials repeatedly end with disappointing results.

Sources: National Library of Medicine; National Institutes of Health; William Amarquaye, University of South Florida; Paul Bieniasz, Rockefeller University; Jeremy Faust, Brigham & Womens Hospital; Matt Frieman, University of Maryland School of Medicine; Noah Haber, Stanford University; Swapnil Hiremath, University of Ottawa; Akiko Iwasaki, Yale University; Paul Knoepfler, University of California, Davis; Elena Massarotti, Brigham and Womens Hospital; John Moore and Douglas Nixon, Weill Cornell Medical College; Erica Ollman Saphire, La Jolla Institute for Immunology; Regina Rabinovich, Harvard T.H. Chan School of Public Health; Ilan Schwartz, University of Alberta; Phyllis Tien, University of California, San Francisco.

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HPU Students, Faculty and Staff Recognized for Research and Innovation – High Point University

August 15th, 2020 9:48 am

HIGH POINT, N.C., Aug. 14, 2020 Members of the High Point University community frequently conduct, publish and share research and creative works in a variety of ways. Below is a recap of recent research initiatives.

HPU Student, Alumna and Faculty Research Featured in National Scientific Journal

Casey Garr, HPU alumna; Candyce Sturgeon, HPU rising senior; Dr. Veronica Segarra, HPU assistant professor of biology; and Noah Franks, student at Penn Griffin School of the Arts in High Point, North Carolina; recently conducted research that was published in Autophagy, a national scientific journal.

The study, titled, Autophagy as an on-ramp to scientific discovery, examines HPUs Cell Art Collaborative program to gain understanding around how the recruitment of highly creative students into STEM fields through connections to art can be a first step in defining a specialized career path that leads to a valuable and unique contribution to science.

In addition to providing experiential learning opportunities for students at HPU to conduct hands-on research and co-author peer-reviewed articles, the Cell Art Collaborative program encourages students in the local community to explore careers that incorporate both science and art, says Segarra. This initiative continues to facilitate conversations around STEAM-based learning environments for educators to take advantage of a wider range of student talents and interests, preparing them to go forth into society as the creative thinkers and problem solvers the world needs.

HPU Students Research Featured in CBE: Life Sciences Education Journal

Clara Primus, a rising junior majoring in biology and Bonner Leader at HPU, recently collaborated with prominent scientists at the Mayo Clinic, University of California Davis and Northwestern to conduct research that was published in CBE: Life Sciences Education, a quarterly journal published by the American Society for Cell Biology. The article, titled, Scientific Societies Fostering Inclusive Scientific Environments through Travel Awards: Current Practices and Recommendations, examines how scientific societies can contribute to a diverse and inclusive workforce.

The research compares and contrasts the broad approaches that scientific societies within the National Science Foundation-funded Alliance to Catalyze Change for Equity in STEM Success (ACCESS) use to implement and assess their travel award programs for underrepresented minority (URM) trainees. Findings will improve collaboration and better position scientific societies to begin addressing some of these questions and learning from each other.

The recommendations included in this research shed light on how even scientific societies can be allies in furthering inclusion efforts, said Primus. Ive spent nearly two years studying equity and diversity, and I hope that I can take the knowledge Ive learned from all of my research to educate my peers at HPU.

HPU Exercise Science Professor Publishes Statement for the American Heart Association

Dr. Colin Carriker, assistant professor of exercise science in HPUs Congdon School of Health Sciences, recently co-authored an American Heart Association (AHA) scientific statement on medicinal and recreational cannabis use published in Circulation.

The statement critically reviews the use of medicinal and recreational cannabis from a clinical but also a policy and public health perspective by evaluating its safety and efficacy profile, particularly in relation to cardiovascular health. The purpose of this scientific statement was to explore the evidence and science pertaining to medical marijuana, recreational cannabis and cardiovascular health to provide physicians and health care providers with the information available to date. While cannabis may have some therapeutic benefits, these do not appear to be cardiovascular in nature. Health care providers would benefit from increased knowledge, education and training pertaining to various cannabis products and health implications, including recognition that cannabis use may, in fact, exacerbate cardiovascular events or other health problems. In this regard, the negative health implications of cannabis should be formally and consistently emphasized in policy, while aligning with the American Heart Associations commitment to minimizing the smoking and vaping of any products and banning cannabis use for youth.

It was an honor to work alongside such a high-quality team of researchers, says Carriker. I want to especially thank our committee chairs, Dr. Robert L. Page II and Dr. Larry A. Allen, as their extraordinary leadership and organization were integral components in the completion and publication of this AHA scientific statement. We publish these statements to counterbalance and debunk misinformation because the public requires high-quality information about cannabis from reputable organizations such as the American Heart Association.

Carriker is the advocacy ambassador for the American Heart Associations Council on Lifestyle and Cardiometabolic Health and served as a member of the writing committee tasked with writing this AHA Scientific Statement initiated by the AHAs Council on Clinical Cardiology.

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Statement By Premier Fahie On COVID-19 Update – Phase II – Government of the Virgin Islands

August 15th, 2020 9:48 am

STATEMENT BY PREMIER AND MINISTER OF FINANCEHONOURABLE ANDREW A. FAHIE

COVID-19 UPDATE- PHASE II

Friday, 14th August, 2020

I say good day and Gods Blessings to all the people of the Virgin Islands.

We thank the Lord our God for his continued blessings in our lives and in our Territory.

The world continues to grapple with the realities of COVID-19 and the BVI, is not immune.

I appreciate what we continue to do together in our little corner of the world to keep ourselves and each other safe.

So far we have only had nine confirmed cases, including one death with 8 recoveriesmost of the cases being classified as imported or related.

Together, we have been able to stem the tide, but we are not out of the woods.

The problem of COVID-19 has not yet been solved.

It remains a real, deadly, imminent threat to all persons in all countries throughout the world.

We continue to see countries rushing forward with haste to open their borders, refusing to close their borders, or disobeying the recommended hygiene and safety protocols, only for them to hastily retreat as they experience a surge of infections in their population.

Can I tell you that right now, the only measures that are scientifically proven to keep us all safe are social distancing, wearing of appropriate masks or shield, and washing our hands regularly?

These measures are simple for us to do, so let us continue to do them.

In all our actions, your Government is being guided by the law, international protocols and international best practice, with guidance from God Almighty.

In particular, we are being guided by the provisions of the Public Health Ordinance, the Quarantine Act and the Infectious Diseases (Notification) Act, all of which are designed to treat with circumstances such as these, and which prescribes measures that should be taken whenever there is the risk of an outbreak of disease.

All of our precautionary measures for protecting our people from the public health threat of COVID-19 are soundly grounded in the law of the land. And, your Government is being very cautious in dealing with this very fluid situation because another round of lockdown can cripple our economy to the point that we may not be able to bounce back.

Indeed, we understand and empathise with the inconvenience and hardship that COVID-19 is causing to everyone; however we must be cognisant of the double-threat to public health and the economy.

In the BVI, we cannot afford another lockdown. It will not be healthy for our economy, economically, socially and healthwise.

We are not immuned to the trickled effect of COVID-19, which is a health issue.

That is why even with the controlled re-entry of Virgin Islands, Belongers, permanent residence and Naturalisaed Overseas Territories citizens, since 2 June 2020 and the full internal re-opening of businesses, we have been moving cautiously, and in a phased way so that we can realistically manage our environment and surroundings in the midst of the New Regular of living and working with COVID-19.

There have been several views from many quarters trying to pressure the Government to open up quickly and to open up now.

But, I want to echo something that the Chief Medical Officer Dr. Irad Potter said to Members of Cabinet, which I think was the most profound statement that caused all of us to pause, he said and I quote,

We must take into consideration what risk we can take. We must take into consideration what risk we can manage. And, we must take into consideration what we can and cannot allow. End of quote.

Your Government intends to concentrate on the areas that united us as a people because only through unity will we get through this pandemic, successfully.

To date we have been able to manage and monitor the process to the point where on behalf of the Cabinet of the Virgin Islands, I can now announce that we are now moving into Phase two of our Restricted Border Re-opening Plan.

We are satisfied that the different Government agencies have the necessary protocols in place as we advance into Phase two of the restricted border controlled process.

We have had Special meetings of the Cabinet on 13th August and we had to continue the meeting on 14th August. These are not easy decisions, as checks and balances are important.

But having been satisfied that we have properly ventilated and learn from lessons in Phase one to strengthen Phase two, on behalf of Cabinet, I wish to make the following announcements:

1. We decided that the Ministry of Health and Social Development instruct the Attorney General's Chambers to draft a new Immigration and Prohibition Order for the period from 15th August, 2020 to 31st August, 2020;

People of the Virgin Islands Cabinet also advised that the National Security Council should not extend the Curfew Order, which expired on 13th August, 2020, thereby re-opening the Territory internally for 24-hours a day, seven days a week.

However, all businesses and individuals must adhere to all of the approved social measures; and Cabinet also advised that the National Security Council will impose restrictions on the movement of vessels within Territorial waters in a manner prescribed by Order.

Let me say here.

We are not out of the woods with COVID-19. People are coming in, in phase one and two.

We must continue to remain vigilant.

We cannot leave any stone unturned with COVID-19.

That is why the social distancing measures must apply. That is why adherence to the health protocol is a must.

This is our opportunity to test the strength of our system, our protocol, our preventative measures and our commitment to a healthy and safe Virgin Islands.

If we all follow the rules, all will be well.

I want to take this time to remind our bikers those on the scoters, all our bikers, that safe riding save lives. Please ensure that you have a scooter licence, ensure that your motorbikes are licensed and insured, always wear a helmet, know your scooters limits, watch your speed, keep your distance from other vehicles, use both brakes, avoid blind spots, always use signals. Our young generation is important to the future of this Territory. When our youth damage themselves, they damage their future potential in the Virgin Islands. Remember Your Life Matters!

Our responsibility as a Government is to keep the people of the Virgin Islands healthy and safe as much is humanly possible during this COVID-19 era and at all times.

I want to thank everyone who continues to help us to be safe during this COVID-19 era.

My Government, Cabinet Members, National Security Council, Attorney General Chambers, Cabinet Office, all Members of the House of Assembly, the Health Emergency Operations Centre, the Government public officers at varying levels, the Joint Information Cell/Government Information Service, industry partners and members of the public for all coming together and doing their part in this fight against COVID-19.

In these Virgin Islands, each of us has a role to play to help our economy and to keep us safe.

Remember we are all in this together, but I must warn again that we are not out of the woods as far as COVID-19 is concerned.

Remember that COVID-19 is not playing around with us and we must not play around with COVID-19

Now that the curfew is lifted, more than ever, and the borders remain closed, with limited entry, we must hold each other accountable to get through this experience together.

This phase is our greatest test and I know with Gods help we will pass this test.

Please be advised that the main point of entry remains the TB Lettsome International Airport.

So, let us continue to work together in the oneness of purpose.

Remember, God is with us, and He is opening doors for us so that we can have a Virgin Islands that generations would be proud of.

As leader of Government business, we will continue to keep you the people informed of our efforts to continue to combat COVID-19 as this remains a fluid situation. We will continue to make adjustments, so that the people of the Virgin Islands will remain safe while we balance our economy starting with the rebooting and the revitalization of our internal economy.

May God continue to bless these beautiful Virgin Islands and the people of the Virgin Islands.

I thank you.

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4 of the best ways to treat diabetes and lower blood sugar – Insider – INSIDER

August 15th, 2020 9:47 am

No matter what type of diabetes you have, the goal of diabetes treatment is to control blood sugars and keep them within the healthy range.

Type 1 diabetes must be treated with insulin, since the pancreas does not produce insulin naturally. People with type 2 or gestational diabetes don't always need insulin treatment, and will often focus on lifestyle changes and oral medications that encourage insulin production or decrease insulin resistance.

With proper access to healthcare, diabetes is highly treatable, says Katherine Araque, MD, an endocrinologist and director of endocrinology of the Pacific Neuroscience Institute at Providence Saint John's Health Center in Santa Monica, California.

Here are the four main ways you can treat and manage your diabetes.

Insulin is a hormone produced in the pancreas in healthy individuals. It helps facilitate the process of converting blood sugar into fuel, so that glucose doesn't build up in the blood.

In people with type 1 diabetes, the pancreas cannot produce insulin, so they need synthetic insulin. This can happen in two ways:

People with type 2 diabetes are treated with insulin when they are unable to control their blood glucose levels with lifestyle changes and medication. Overall, roughly 24% of people with diabetes are treated with insulin, according to a 2018 study published in Diabetes Care.

If you need insulin, your doctor will provide specific guidance on how much you need and when you should take it.

Although people with type 1 diabetes will need insulin, they may also be prescribed medication if they have some remaining pancreas function. The medication can encourage insulin production in the body.

People with type 2 diabetes are prescribed medication when they can't control their blood sugars through diet and exercise. Oftentimes, people with type 2 diabetes use more than one medication to control their condition.

However, medications are usually not recommended for pregnant people with gestational diabetes.

Common medications used to treat diabetes include:

Metformin is the most common medication used to treat type 2 diabetes. It's sometimes used to treat type 1 diabetes in people who still have some insulin production, along with insulin.

Metformin helps control blood sugar by making it easier for the body to absorb glucose. It's usually taken twice a day, with meals. Even when used alone, metformin can reduce A1C levels by 1.5% on average, which is enough to drop blood sugar levels from diabetes to prediabetes.

Sulfonylureas are a class of drugs that encourage the pancreas to release more insulin. They're used to treat type 2 diabetes. They are often taken once or twice a day before meals.

Sulfonylureas have a similar efficacy to metformin, and can be used alongside it.

TZDs make it easier for the body to use insulin; they reduce insulin resistance. They can be used to treat type 2 diabetes. They are taken 1 to 2 times per day.

After a year of taking TZDs, people with type 2 diabetes reduced their A1C levels by 1.4%, according to a 2019 study published in Vascular Health Risk Management.

Exercise is important for people with all types of diabetes. "Exercise helps at multiple levels: it increases base metabolic rate, fights insulin resistance, and helps with weight loss," says Araque.

Exercise helps muscles burn glucose and reduces insulin resistance. When you exercise, your muscles burn more glucose, removing it from the bloodstream and helping to lower blood sugar levels.

For example, a 2017 study published in Biomedical Research followed 120 obese teens, who did two hours of aerobic exercise twice a day for six days a week. After five weeks, their average fasting blood sugar was reduced by 0.84 nanomoles per liter (nmol/L) for males and 1.04 nmol/L for females. The researchers described this as "an extremely significant difference."

The Center for Disease Control and Prevention (CDC) recommends that people with diabetes get the normally recommended amount of exercise: 150 minutes of exercise each week, including two days of strength workouts that incorporate major muscle groups. The American Diabetes Association recommends starting with small changes, like walking daily.

Any exercise will help, but some may be especially beneficial. For example, a 2019 study published in Diabetologia found that afternoon exercise decreased blood sugars more than morning exercise.

Overall, you should work with your doctor to identify an exercise program that will benefit you, Araque says.

Healthy eating is critical for people with diabetes. As food breaks down, it releases glucose into your blood. Some foods, including processed sugars and carbohydrates, raise blood sugars more than other foods, like proteins or leafy vegetables.

In particular, people with diabetes need to be aware of how many carbs they eat per day. They should also create an eating plan that includes the following:

For example, the DASH diet and Mediterranean diet which both emphasize healthy fats, lean protein, protein and vegetables have been proven to help people with type 1 and type 2 diabetes control blood sugar.

Read more about the best ways to eat if you have diabetes:

Diabetes is a chronic but manageable condition, Araque says. People with diabetes should work with their doctor, nutritionist, and an exercise professional to design a program that meets their needs.

"The most important message is if they follow these recommendations they can get this under control and decrease risk for complications," Araque says. "Patients should have hope."

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MENTAL HEALTH MATTERS: Depression and diabetes: Are they linked? – Sherman Denison Herald Democrat

August 15th, 2020 9:47 am

Recent research in the Journal of Medicine (2016) has shown us that rates of depression can be twice as high in people with type 2 diabetes than in the general population. So, whats the missing link here? Why do people with diabetes tend to experience more issues with depression?

To start, the Stand American Diet is closely tied to the development of T2D. In a study published in 2017, people who regularly consumed red meat, processed meat, sugar sweet beverages (SSB), and eggs showed to have two times the risk of T2D. Also, people who added to their diet whole grains, vegetables, fruits, and dairy showed a 42% reduction compared to the prior group. Perhaps most amazing in this study is that people who combined both not eating the unhealthy foods and adding in the healthy foods, showed a whopping total risk reduction of 70%! (European Journal of Epidemiology).

Now, consider that studies have also shown that the Standard American Diet is tied to depression. High consumption of red and/or processed meat, refined grains, sweets, high-fat dairy products, butter, potatoes and high-fat gravy, and low intakes of fruits and vegetables is associated with an increased risk of depression (Psychiatry Research 2017). Alcohol, as well, can play a part given that increased use has shown an increased risk of depression (Addiction 2011). Epidemiological evidence suggests a strong connection between diet quality and mental health across multiple populations and age groups (the Nutrition Society 2017).

Diabetes is a chronic health condition that prevents insulin from allowing glucose into muscle cells in the body. Glucose (a monosaccharide sugar) is the major energy source of the body. People with type two diabetes (T2D) cannot properly use the insulin their bodies make, resulting in too much glucose circulating in the bloodstream. Over time, this can cause serious health problems. In 1958, less than one percent of the U.S. had diabetes. By 2019, that number had grown to 13% a 1200% increase!

It has also been suggested that the effect of exercise also may be comparable to antidepressant medication and psychotherapy for mild to moderate depression. As well, exercise seems to be a valuable complementary therapy to the traditional treatments for severe depression (Disability Rehabilitation, 2015). Other studies have also shown that unhealth eating habits along with tobacco smoking and lower levels of physical activity are major contributors to chronic disease and mortality (Schizophrenia Research, 2018).

What all of this tells us that the missing link between depression and type 2 diabetes is something we actually have some control over. Simply lifestyle choices that we can make can prevent the majority of T2D and have profound effects on depression symptoms. Eating a healthy diet, not smoking, low consumption of alcohol, and moderate exercise can reduce the risk of T2D by 91% (New England Journal of Medicine). Changing what we eat can actually provide a clinically significant benefit to traditional forms of treatment for both diabetes and depression.

Jim Runnels is a retired Licensed Professional Counselor and advocate of evidence-based education and supporter of the health benefits of a whole food plant-based, active lifestyle, to achieve optimal health. He is the administrator of Eat Healthy-Texoma Facebook page. The views and opinions expressed here are the authors own and do not necessarily reflect those of the Herald Democrat.

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Diabetes Linked to Increased Kidney Cancer Risk, But Only in Slim – Medscape

August 15th, 2020 9:47 am

Diabetes increases the risk of kidney cancer in postmenopausal women, but paradoxically, only in nonobese women, as defined by body mass index (BMI) and waist circumference, according to a new analysisfrom the Iowa Women's Health Study (IWHS).

"Many studies have linked a history of diabetes to the increased risk of kidney cancer [but] it is unclear whether diabetes is a risk factor for kidney cancer independent of other risk factors such as obesity and hypertension," write Shuo Wang, PhD, of the School of Public Health, University of Minnesota, Minneapolis, and colleagues.

"[While we found that] an association between diabetes and kidney cancer was not statistically significant among the whole cohort...a positive, statistically significant association was observed among nonobese women (BMI < 30 kg/m2) or waist circumference < 34.6 inches (87.9 cm)," the authors suggest.

And although they acknowledge "these findings should be validated in larger or pooled prospective studies," they stress that "patients with new-onset diabetes may require more thorough surveillance for cancer including kidney cancer."

The results were published online August 11 in Maturitas.

The IWHS was launched in 1986 when a baseline questionnaire was completed by a total of 41,836 women.

Subsequent questionnaires were mailed in 1987, 1989, 1992, 1997, and 2004, returned by increasingly fewer respondents over the years.

The cohort for the current analysis included 36,975 women, mean age of 61.7 years, 6.4% of whom reported adiabetes diagnosisat baseline.

"At baseline, diabetes status was determined for each participant by one of two ways," the researchers explain.

Women were first asked if a physician had ever told them they had diabetes and were also asked whether they took pills for diabetes and/or insulin. A tape measure was included with the baseline questionnaire and women were asked to have their waist measured in a precise manner with a high degree of accuracy and reliability.

Between 1986 and 2011, investigators identified 257 cases of kidney cancer in their cohort.

They then examined the association between baseline and time-dependent diabetes and kidney cancer risk using three models, the first adjusted only for age, the second adjusted for age and BMI tertile, and the third was a multivariable-adjusted model.

The adjusted variables in the third model included age and indices of obesity, as reflected by BMI and waist-to-hip ratio (WHR), as well as physical activity levels, pack-years of smoking, total caloric intake, presence of hypertension, diuretic use, and alcohol intake.

Cutoffs used to define obesity included a BMI of 30 kg/m2, a WHR of 0.85, and a waist circumference of 34.6 inches.

Researchers also analyzed the association between duration of diabetes and kidney cancer risk using a nested-case control design within the IWHS cohort.

Over the course of follow-up, an additional 8.5% of women reported a new diagnosis of diabetes.

"Several characteristics were statistically significantly associated with kidney cancer risk," the authors note (Table 1).

"And time-dependent diabetes was associated with an increased risk of kidney cancer in models 1 and 2," they added.

Table 1. Increased Kidney Cancer Risk, Baseline Characteristics (Models 1, 2)

*4 grams/day of alcohol

BMI = body mass index; WHR = waist-hip ratio

However, when investigators adjusted the association between time-dependent diabetes and kidney cancer risk in model 3, associations seen in models 1 and 2 were attenuated and no longer significant, the authors underscore.

In contrast, the risk of kidney cancer increased for women with diabetes.

Compared to women without diabetes, women with diabetes and a BMI < 30 kg/m2 had an 82% higher risk of kidney cancer, and those with diabetes and a waist circumference < 34.6 inches had an over twofold greater risk (Table 2).

Table 2. Interaction Between Diabetes, Weight in Kidney CaRisk (Model 3)

BMI = body mass index; HR = hazard ratio; WC = waist circumference

As the investigators point out, there are a number of possible explanations for these seemingly paradoxical findings.

Type 2 diabetes is associated with high blood glucose, which itself may increase uncontrolled cell growth and division.

This may help explain why investigators saw a stronger association with kidney cancer among those with a shorter diabetes duration, that is, "those who are more likely to have uncontrolled diabetes," they explain.

Investigators also point out: "Patients with type 2 diabetes (the majority of diabetes cases in our study) have high serum levels of insulin that promote the secretion and production of insulin-like growth factor 1 (IGF-1)."

IGF-1 is important in the regulation of cell proliferation and differentiation, and thus may promote the formation and growth of cancer, they add.

But there is a "nonlinear relationship between BMI and IGF-1 levels," the investigators observe. For example, one study found that IGF-1 concentrations in women increased as BMI increased up to a maximum of 26 kg/m2, after which IGF-1 concentrations decreased among women with higher BMIs.

"In line with this finding, we found an association among nonobese women...even in the fully adjusted model, but observed no association between diabetes and kidney cancer among obese women...which could be explained by lower levels of IGF-1 among obese women."

Previous epidemiologic findings from the IWHS did find evidence of an association between weight-related measures and kidney cancer risk; however, those with a BMI in the top quartile had an almost 2.5-fold greater risk of kidney cancer than those in the lowest BMI quartile.

The study was funded by the National Cancer Institute. The authors have reported no relevant financial relationships.

Maturitas. Published online August 11, 2020. Abstract

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How to lower your blood sugar quickly and what to do if it’s an emergency – Insider – INSIDER

August 15th, 2020 9:47 am

If you have diabetes, your body isn't able to regulate blood sugar properly, either because the pancreas doesn't produce insulin (type 1 diabetes) or the body has become resistant to it (type 2 diabetes).

As a result, people with diabetes have to carefully manage their blood sugar levels through diet, exercise, and medications to make sure it stays in a healthy range.

But sometimes, blood sugar can become too high. In many of these cases, people with diabetes will be able to quickly lower blood sugar on their own, by taking more insulin. However, other times, they may need to visit the ER for immediate medical attention.

Here's how to tell if your blood sugar is too high and what you'll need to do in order to lower it quickly.

People with diabetes are considered to have high blood sugar, or hyperglycemia, if blood glucose levels are higher than:

While there are other conditions that can cause hyperglycemia, it is most commonly linked to both type 1 and type 2 diabetes. That's why it is important for people with diabetes to check their blood sugar using blood glucose meters with the goal of keeping levels from getting too low or too high.

In addition, there are other signs and symptoms of high blood sugar you might notice.

The most common symptoms of hyperglycemia are:

"If someone has hyperglycemia, it would mean they would be very thirsty, tired, they might be urinating more frequently and basically not feeling well," says Sam Zager, M.D. a family medicine physician in Maine.

Hyperglycemia is not automatically an emergent situation. Anyone with diabetes knows high blood sugar readings will happen, and it's okay, as long as it doesn't last too long or get too high.

If it does occur, here are a few ways to quickly lower blood sugar on your own:

Insulin can be used to treat acute cases of high blood sugar for people with diabetes.

People with type 1 diabetes (who always use insulin) and some people with type 2 diabetes (who sometimes use insulin) can give themselves an extra dose of insulin to quickly lower their blood sugar to safer levels. How much to take depends on the situation and what your doctor recommends.

When you have high blood sugar, you may experience frequent urination as your body tries to get rid of the extra glucose. Losing this fluid can cause dehydration and make hyperglycemia symptoms even worse.

It's important to drink water when you have hyperglycemia in order to stay hydrated and help your body regulate and lower blood sugar. But drinking lots of water won't necessarily lower blood sugar on its own. For more information, read about how much water you're supposed to drink a day.

Exercise isn't always the safest or most effective way to quickly lower blood sugar. It is important to note that exercise only works if there is insulin present, whether naturally or through injection, so that glucose can get into the cells to be metabolized.

If there is no insulin, your body will start burning fat for energy, and this could lead to a dangerous condition called diabetic ketoacidosis. People with type 1 diabetes should not exercise if they have hyperglycemia.

However, exercise can lower blood sugar for most people with diabetes it just shouldn't be used in emergency situations. In a 2013 study in the journal Diabetes Care, more than 5,000 people with diabetes recorded their blood glucose levels before and after exercising for as little as 10 minutes. Overall, more than 75% of people saw their level decrease an average of about 17%.

Overall, Zager says that exercise is important for managing diabetes, but warns that it isn't a great short-term fix. For more information on how to control blood sugars in the long-term, learn about the 6 best ways to lower blood sugar naturally.

For people with type 1 diabetes, untreated high blood sugar can lead to a life-threatening condition called diabetic ketoacidosis, or DKA.

When there is no insulin and glucose can't get into cells, your body starts breaking down fat into a fuel called ketones. If ketones build up in your blood, it becomes dangerously acidic. DKA can cause very serious health complications such as fluid building up in the brain, kidney failure, and cardiac arrest.

If your blood sugar is above 240 mg/dL, you should check your urine for ketones, a sign you may be at risk for DKA. You can do this with an at home test, but you also should contact your doctor. If there are ketones in your urine, you should go to the emergency room. Other symptoms of DKA include:

In rare occasions, DKA can occur in people with type 2 diabetes, but the more common complication for people with type 2 is called hyperglycemic hyperosmolar state, or HHS. HHS occurs when blood glucose levels are high for an extended period of time. The extra sugar is passed into the urine, causing the person to urinate frequently and become severely dehydrated, just like with DKA.

For people with type 2 diabetes, blood sugar above 600 mg/dL indicates HHS. Other symptoms include:

These symptoms generally come on slowly, but you should contact your doctor immediately. In the ER, doctors will likely use insulin to lower your blood sugar, as well as give you fluid and electrolytes, to keep your heart, kidneys, muscles, and nerve cells functioning properly.

For people with diabetes, a single instance of high blood sugar is generally not an emergency, as long as it is addressed. Usually, taking an extra dose of insulin will quickly lower your blood sugar back to normal levels. However, if you are on insulin and run out, or have symptoms of DKA or HHS, you should get medical attention right away.

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OSA Severity Reduced in Type 2 Diabetes With Lifestyle Interventions for Weight Loss – Pulmonology Advisor

August 15th, 2020 9:47 am

The use of intensive lifestyle intervention for weight loss in patients with type 2 diabetes has been shown to reduce the overall severity of obstructive sleep apnea (OSA), according to study results published in the American Journal of Respiratory and Critical Care Medicine.

Researchers conducted the longitudinal randomized controlled Sleep AHEAD study (ClinicalTrials.gov Identifier: NCT00194259) an ancillary study of Look AHEAD (Action for Health in Diabetes) enrolled participants from 4 of the 16 Look AHEAD sites.

Investigators sought to establish whether initial benefit of intensive lifestyle intervention for weight loss on OSA severity would be maintained at 10 years. The primary study objective was to determine whether the Look AHEAD intervention was associated with improvements in apnea-hypopnea index (AHI) at 10 years and during the 10-year follow-up. Secondary objectives included determining whether this effect was independent of weight change and whether the intervention had an effect on changing an individuals OSA category.

Primary study inclusion criteria of Look AHEAD (and, thus, of Sleep AHEAD) were being between ages 45 and 7, having a body mass index (BMI) of 25 kg/m2 (or 27 kg/m2 if taking insulin), physician-verified type 2 diabetes, and hemoglobin A1c of <11%. Participants received either intensive lifestyle intervention for weight loss or diabetes support and education (DSE). Of the 264 participants, 38.7% had mild OSA, 35.2% had moderate OSA, and 26.1% had severe OSA at baseline.

At 10 years, polysomnograms were obtained in 54% of those in the intensive lifestyle intervention group and in 48% of those in the DSE group. Mean weight losses in the intensive lifestyle intervention group at 1, 2, 4, and 10 years were 10.70.7 kg, 7.40.7 kg, 5.10.7 kg, and 7.10.8 kg, respectively. These weight losses were all significantly higher than the 1-kg weight loss at 1, 2, and 4 years, and the 3.50.8 kg weight loss at 10 years in the DSE group (P .0001).

The AHI was lower with intensive lifestyle intervention compared with DSE by 9.72.0, 8.02.0, and 7.92.2 events per hour at 1, 2, and 4 years, respectively (P .0004), and by 4.02.5 events per hour at 10 years (P =.109). Changes in AHI over time were associated with the amount of weight loss, baseline AHI, and year of the visit (P <.0001), as well as with the intervention independent of change in weight (P =.01). At 10 years, OSA remission occurred in more participants in the intensive lifestyle intervention compared with participants in DSE group (34.4% vs 22.2%, respectively).

The investigators concluded that although the greater improvement in OSA severity with intensive lifestyle intervention in the initial 4 years was no longer present at the 10-year follow-up and the greater weight loss in the intensive lifestyle intervention group also diminished at 10 years, overall OSA severity decreased across the 10-year study period with intensive lifestyle intervention. This improvement was associated with changes in body weight, greater severity of baseline OSA, and lifestyle intervention unrelated to weight change.

Reference

Kuna ST, Reboussin DM, Strotmeyer ES, et al; for the Sleep AHEAD Research Subgroup of the Look AHEAD Research Group. Effects of weight loss on obstructive sleep apnea severity: 10-year results of the Sleep AHEAD study. Am J Respir Crit Care Med. Published online July 28, 2020. doi:10.1164/rccm.201912-2511OC

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Impact of COVID-19 on the Global Diabetes Assays Industry 2020-2030 Featuring Siemens Healthineers, Abbott Labs, Roche, Danaher and Tosoh -…

August 15th, 2020 9:47 am

DUBLIN--(BUSINESS WIRE)--The "Diabetes Assays (In Vitro Diagnostics) - Global Market Analysis and Forecast Model (COVID-19 market impact)" report has been added to ResearchAndMarkets.com's offering.

This market model discusses in detail the impact of COVID-19 on Diabetes Assays market for the year 2020 and beyond.

Companies Mentioned

Hemoglobin (HbA1c) assays are the most commonly used for both initial and confirmatory screening of diabetes across all geographical regions. The American Diabetes Association (ADA) recommends HbA1c tests 2 times per year in patients who are meeting treatment goals and additional testing for patients who are not meeting their treatment goals. Screening may be repeated every three years in patients that have normal test results.

Each of the covered 39 country's color-coded and fully-sourced market models are equipped with epidemiology based indications with procedure volumes. To increase the data transparency, the interactive excel deliverable covers installed base, new sales volumes, product usage, average selling prices, market size and company share/rank analysis (wherever available). Moreover, analyst comments with qualitative insight offer context for quantitative data.

Key Inclusions of the market model are:

Currently marketed Diabetes Assays and evolving competitive landscape.

Global, Regional and Country level market specific insights.

Drive the understanding of the market by getting the veritable big picture including an overview of the healthcare system. In addition the Market Access segment allows you to delve deeper into market dynamics with information on reimbursement policies and the regulatory landscape.

Robust methodologies and sources enable the model to provide extensive and accurate overview of the market. Demand and supply-side primary sources are integrated within the syndicated models, including Key Opinion Leaders. In addition, real world data sources are leveraged to determine market trends; these include government procedure databases, hospital purchasing databases, and proprietary online databases.

Reasons to Buy

The model will enable you to:

For more information about this report visit https://www.researchandmarkets.com/r/awtz02

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DarioHealth Announces Poster Presentation at the Virtual Association of Diabetes Care and Education Specialists 2020 Annual Conference – PRNewswire

August 15th, 2020 9:47 am

NEW YORK, Aug. 13, 2020 /PRNewswire/ -- DarioHealth Corp. (Nasdaq: DRIO), a pioneer in the global digital therapeutics market, today announced that an emerging science industry poster has been accepted for presentation at the virtual Association of Diabetes Care and Education Specialists (ADCES) 2020 Annual Conference, which is being held today, August 13, through August 16, 2020.

The poster, entitled, "Impact of Digital Management on Clinical Outcome in Patients with Chronic Conditions: Diabetes and Hypertension," details results from an observational study of 345 participants with hypertensive blood pressure at baseline who utilized the Dario digital therapeutics platform.

Results:

Blood pressure

Diabetes

Notably, the average age of participants in this study was 60.4 years, suggesting that the required use of technology by older individuals does not appear to be a significant barrier to engagement.

The paper concludes, "This observational study of a digital therapeutic platform for chronic disease demonstrates improved blood pressure at three months and glycemic control at six months compared to baseline. These findings suggest that digital therapeutics may help sustain behavioral change and play an important role in the management of diabetes and hypertension."

Erez Raphael, Chief Executive Officer of Dario, stated, "We are excited about these positive results observed across hundreds of patients. We believe that this latest study adds to our growing body of clinical evidence, supporting the use of Dario's platform to produce meaningful health improvements in patients who are trying to better manage their chronic conditions such as hypertension and diabetes. We believe that this information is not only helpful to the physicians who recommend use of our platform, but also to institutions like payers and self-insured employers who benefit from healthier members and employees in the form of reduced medical expenses. This value proposition is an important tool for attracting new clients in our Business-to-Business-to-Consumer (B2B2C) channel."

About DarioHealth Corp.

DarioHealth Corp. (Nasdaq: DRIO) is a leading, global digital therapeutics company revolutionizing the way people with chronic conditions manage their health. By delivering evidence-based interventions that are driven by data, high-quality software and coaching, we empower individuals to make healthy adjustments to their daily lifestyle choices to improve their overall health. Our cross-functional team operates at the intersection of life sciences, behavioral science and software technology to deliver highly engaging therapeutic interventions. Dario is one of the highest-rated diabetes solutions in the market, and its user-centric MyDariomobile app is loved by tens of thousands of consumers around the globe. DarioHealth is rapidly moving into new chronic conditions and geographic markets, using a performance-based approach to improve the health of users managing chronic disease. To learn more about DarioHealth and its digital health solutions, visithttp://dariohealth.com

Cautionary Note Regarding Forward-Looking Statements

This news release and the statements of representatives and partners of DarioHealth Corp. (the "Company") related thereto contain or may contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Statements that are not statements of historical fact may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as "plan," "project," "potential," "seek," "may," "will," "expect," "believe," "anticipate," "intend," "could," "estimate," or "continue"are intended to identify forward-looking statements. For example, the Company is using forward-looking statements in this press release when it discusses its belief that the study adds to its growing body of clinical evidence, supporting the use of Dario's platform to produce meaningful health improvements in patients who are trying to better manage their chronic conditions such as hypertension and diabetes, its belief that the information is not only helpful to the physicians who recommend use of its platform, but also to institutions like payers and self-insured employers who benefit from healthier members and employees in the form of reduced medical expenses and that the value proposition is an important tool for attracting new clients in the its B2B2C channel.Readers are cautioned that certain important factors may affect the Company's actual results and could cause such results to differ materially from any forward-looking statements that may be made in this news release. Factors that may affect the Company's results include, but are not limited to, regulatory approvals, product demand, market acceptance, impact of competitive products and prices, product development, commercialization or technological difficulties, the success or failure of negotiations and trade, legal, social and economic risks, and the risks associated with the adequacy of existing cash resources. Additional factors that could cause or contribute to differences between the Company's actual results and forward-looking statements include, but are not limited to, those risks discussed in the Company's filings with the U.S. Securities and Exchange Commission. Readers are cautioned that actual results (including, without limitation, the timing for and results of the Company's commercial and regulatory plans for Dario) may differ significantly from those set forth in the forward-looking statements. The Company undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by applicable law.

DarioHealth Corporate Contact:Claudia LeviContent & Communications Manager[emailprotected]+1-347-767-4220

Media Inquiries:Investor Relations Contact:Chuck Padala[emailprotected]+1 646-627-8390

SOURCE DarioHealth Corp.

https://www.dariohealth.com/

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Diabetes Drug Market 2020: Potential Growth, Challenges, and Know the Companies List Could Potentially Benefit or Loose out From the Impact of…

August 15th, 2020 9:47 am

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Diabetes type 2 warning – do your feet look like this? The sore patches of skin – Express

August 15th, 2020 9:47 am

Type 2 diabetes could be caused by the body not producing enough of the hormone insulin, or the body not reacting to insulin.

Without enough of the hormone, the body struggled to convert sugar in the blood into useable energy.

It's crucial that if you think you may have diabetes, you speak to a doctor as soon as possible.

You may be at risk of the condition if you notice some changes to the skin on your feet.

READ MORE: Type 2 diabetes symptoms - the major sign in your thighs

"Constantly feeling thirsty, weeing all the time and feeling really tired; these are all symptoms that should lead us to think about diabetes," warned Benenden Health's society matron, Cheryl Lythgoe.

She told Express Health: "However, when it comes to diabetes, there are many other symptoms that should be getting our attention too.

"For example, if you struggle with one infection after another - a wound infection that wont settle or a fungal infection such as thrush or athlete's foot, for example this could be a symptom of diabetes.

"All of these signs and symptoms could be an indicator of diabetes and would require a discussion and some testing with your GP."

Many people may have diabetes without even knowing it, because the signs and symptoms dont necessarily make you feel unwell.

Common diabetes symptoms include having cuts or wounds that take longer to heal, having an unquenchable thirst, and passing more urine than normal.

You should speak to a doctor if youre worried about the warning signs or symptoms of diabetes, or if you think you may be at risk.

Diagnosing the condition early is very important, because patients are more at risk of some deadly complications, including heart disease and strokes.

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Genetic Variants and the Biology of Stillbirth – Technology Networks

August 14th, 2020 2:50 pm

Columbia researchers have uncovered an array of new genes that cause stillbirth, significantly increasing the understanding of the condition's genetic foundations. The findings suggest that genetic analysis could be used to counsel parents who have previously experienced stillbirth and to unlock new human biology.

Using both standard and advanced analysis techniques, the team led by David Goldstein, PhD, and Ronald Wapner, MD, of Columbia University Vagelos College of Physicians and Surgeons (VP&S) identified the likely genetic cause of stillbirth in about one of every 10 cases studied.

"This study shows that careful genetic analyses can often identify the precise genetic causes of stillbirth and demonstrates the importance of diagnostic sequencing in all cases of unexplained stillbirth," says Goldstein, director of the Institute for Genomic Medicine at Columbia University Irving Medical Center. "Of equal importance, the work highlights how little we currently understand about the biology of stillbirth and the role that genomic analysis can play in helping us understand it."

The study was published online today in the New England Journal of Medicine by the Columbia team. Kate Stanley, MS, a research associate in the Goldstein lab, and Jessica Giordano, MS, a research genetic counselor in the reproductive genetics division of the Department of Obstetrics & Gynecology at VP&S, were co-first authors of the study.Presumed Genetic Underpinning, but Few Studies

Stillbirth (the in utero death of a fetus after 20 weeks' gestation) occurs in approximately one in 100 pregnancies and is about 10 times more common than sudden infant death syndrome.

But in the majority of cases, the cause of stillbirth is unknown. Some have been linked to maternal medical conditions such as infection and preeclampsia; 10% to 20% are attributed to large and easily detectable chromosomal abnormalities. Only a few genes have been implicated.

"Unlike postnatal childhood conditions that are presumed to be strongly genetic, stillbirth had yet to be systematically analyzed with modern genome sequencing approaches," says Goldstein.

"All too often, we have no explanation to give parents who experience a stillbirth," says Wapner, professor of obstetrics & gynecology. "Not only are they devastated, they're often left to wonder if it's something they did wrong or if it might happen again."

Genomic Sequencing Plus New Bioinformatic Analyses Find Hidden Genetic Causes

Genomic sequencing has been particularly useful in diagnosing otherwise unexplained childhood disorders and fetal structural defects, and the Columbia team used it for the first time to search for genetic variants that cause stillbirth.

The researchers sequenced all protein-encoding genes--where most known disease-causing genetic variants occur--from 246 stillborn fetuses and deployed new statistical analyses to identify the genetic mutations that caused the death of the fetus.

The combination of traditional sequencing and new analytical techniques revealed small changes in 13 genes that caused fetal death; six of the genes had not been previously linked to stillbirth.

"Although these are small changes in only a single site in the genome, they are, in effect, genomic sledgehammers that either dramatically change or knock out essential genes and appear responsible on their own for fetal demise," Goldstein says.

The small genetic changes explained 8.5% of the stillbirths in the study. When combined with a previous analysis of larger genomic alterations in this group, the researchers determined that 18% of the stillbirths had a known genetic cause.

The analysis also showed a critical difference compared with the study of postnatal genetic conditions.

"Interestingly, some of the changes we found in genes known to cause postnatal diseases and conditions appeared to have more profound effects than the mutations linked to postnatal disease," Goldstein adds.

Clinical Implications

Currently, the analyses required to find causal genetic causes of a stillbirth can be conducted in only a few academic medical centers.

But eventually the findings from this study--and future studies--will help physicians counsel parents and guide clinical care.

"To a woman who's just had a stillbirth, specific knowledge about the cause is critical," Wapner says. "They often blame themselves and some decide not to have any more children."

If the stillbirth can be attributed to a genetic mutation that has only occurred in the fetus, not in the parents, the same problem is unlikely to occur in future pregnancies.

"That knowledge would change the way we would provide care," Wapner says, "and facilitate closure and bereavement for families."

Unlocking New Human BiologyMost genetic diagnostic studies focus on genes already known to cause disease. Because stillbirth has been understudied, however, the team wanted to test whether genetic changes in genes not currently linked to disease contribute to stillbirth.

For this assessment, the researchers used a bioinformatic tool pioneered by the Goldstein lab that focuses on genes that are under the strongest natural selection in the human population--known as "intolerant" genes. The lab team showed that at least 5% of stillbirths are likely explained by mutations in intolerant genes that are not currently linked to any known human disease.

"These novel disease genes appear to be critical for early human development, and the only way to discover them is through the analysis of fetuses that do not develop," Goldstein says.

"We're opening up new frontiers in biology and the more we understand about basic human development, the more we can potentially intervene."

Reference: Stanley et al. (2020).Causal Genetic Variants in Stillbirth. The New England Journal of Medicine.DOI: 10.1056/NEJMoa1908753.

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

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Evaluating the Role of Genetics in Pediatric Suicidal Ideation and Aggression – Psychiatry Advisor

August 14th, 2020 2:50 pm

Genetic variation combined with elevated aggression scores may predict childhood suicidal thoughts, while suicidal thoughts in childhood may point to young adult depression, according to data published in the Journal of Affective Disorders.

Researchers at the University of Pennsylvania wanted to determine if suicidal ideation in childhood was associated with genes indicative of suicidal ideation in adults. They also wanted to determine if aggression played a role in childhood suicidal thoughts.

A psychiatric disorder is present in more than 90% of adult suicides, according to the investigators, and aggression is associated with increased suicidal behaviors in both children and adults. Uncovering the role of childhood suicidal behavior on the development of psychiatric disorders later in life, as well as the influence of aggression, could help with suicide prevention efforts.

A total of 478 participants aged 8 through 18 years enrolled in the study and received ongoing assessment until age 19. Using multiple behavior assessment tools, researchers found that 25.9% of participants reported suicidal thoughts during 1 or more visits. These thoughts occurred for the first time at a median age of 13 years (mean age, 12.72.9 years; range, 8-18 years). Of the 17 children that attempted suicide, 10 reported aggression. Results of a Cox Survival analysis demonstrated a significant association between childhood aggression and suicide attempts.

To determine the role of genetics in the onset of suicidal thoughts, investigators tested specific haplotypes within ANKK1-DRD2 and HTR2C as potential predictors of suicidal thoughts and behaviors. Structural equation model results demonstrated that 3 single nucleotide polymorphisms (SNPs) within the HTR2C gene, 1 SNP in the ANKK1 gene, and 2 haplotypes AAAC in the ANKK1-DRD2 complex and the CCC haplotype in the HTR2C gene were significantly associated with suicidal ideation in childhood.

Limitations of the study include the relatively small sample size and the use of assessments conducted between 1990 and 2010, which does not account for the rise in suicide rates over the past decade.

Using genetic sequencing, researchers found specific haplotypes within ANKK1-

DRD2 and HTR2C genes are associated with either risk or resilience to developing suicidal

thoughts in childhood, depending on the individuals genetic background. Determining overall levels of aggression further helps determine which children will develop suicidal thoughts.

These observations have the potential to provide a framework for precision medicine that utilizes both genetic variation and phenotypic markers for early intervention and treatment, the researchers concluded.

Reference

Hill SY, Jones BL, Haas GL. Suicidal ideation and aggression in childhood, genetic variation and young adult depression [published online July 24, 2020]. J Affect Disord. doi: 10.1016/j.jad.2020.07.049

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Genetics survival game Niche comes to Switch on the 3rd September – Gamasutra

August 14th, 2020 2:50 pm

[This unedited press release is made available courtesy of Gamasutra and its partnership with notable game PR-related resource GamesPress.]

14th August - Zurich, Switzerland - Indie team Stray Fawn Studio (Nimbatus) today announced that their genetic survival sim Niche will be coming to Nintendo Switch! It will release on the 3rd September and pre-orders with a 10% discount are available now. The initial Steam release was met with great player feedback and currently has over 2700 users reviews, ranking the game as very positive.

Niche is a colourful genetic survival game about selectively breeding and evolving an adorable species of creatures to keep them alive against all odds, such as hungry predators, climate change and sickness. Combining turn-based strategies with simulation and roguelike elements, the game provides tons of different approaches to survive in the harsh environment.

Stray Fawn Studios game designer Philomena Schwab always had a strong affinity for biology and even struggled for a time to decide whether she wanted to pursue that field or game design. As a result, she decided to create Niche, a game about population genetics with a mating system based on real gene science, featuring mutation, dominant/recessive/codominant heredity and much more.

With a genetics system based on real DNA, the PC version of the game is currently also free for teachers to use in classrooms and is used by over 300 biology teachers for their studies.

Nintendo Switch review codes are available via [emailprotected] for editorial outlets.

Game features:

About Stray Fawn Studio

Stray Fawn Studio is an indie team from Zurich, Switzerland led by Micha Stettler and Philomena Schwab, with a focus on procedural world generation and creative freedom of the player.

Their first game Niche was initially released on Steam in September 2016, and since then

Stray Fawn Studio has delivered two other games, Nimbatus and Retimed.

The studio is now working on the Switch release for Niche, and a super-duper special unannounced project.

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