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Nightingale Health to analyze biomarker profiles of 500,000 blood samples from UK Biobank

Comprehensive metabolic biomarker profiles of the world's largest health database to be analyzed in 30 months.

22 Jun 2018

New guidelines recommend newborns with Down’s syndrome to receive leukemia test

New genetic testing has been developed at the University of Oxford to detect early signs of a potentially fatal condition that can also develop into full blown leukaemia in children with Down’s syndrome.

21 Jun 2018

Follow-up study confirms success of physiological test for autism

One year after researchers published their work on a physiological test for autism, a follow-up study confirms its exceptional success in assessing whether a child is on the autism spectrum.

19 Jun 2018

Single blood sample can provide adequate confirmation of diabetes

The study, published June 19 in the journal Annals of Internal Medicine, found evidence that a positive result for two standard diabetes markers in a single blood sample is a highly accurate predictor of diabetes and of major diabetes complications such as kidney disease and heart disease.

19 Jun 2018

Novel chip can be used to identify rhinovirus strains as cause of asthma

MedUni Vienna has developed a method that can be used to identify individual rhinovirus strains ("cold viruses") as a cause of asthma.

18 Jun 2018

Technology breakthrough could enable detection of fetal genetic abnormalities in early pregnancy

A wide range of fetal genetic abnormalities could soon be detected in early pregnancy thanks to a world-first study led by University of South Australia researchers using lab-on-a-chip, non-invasive technology.

18 Jun 2018

Researchers link red meat sensitivity spread by ticks with heart disease

University of Virginia School of Medicine researchers have linked sensitivity to an allergen in red meat - a sensitivity spread by tick bites - with a buildup of fatty plaque in the arteries of the heart.

18 Jun 2018

Researchers discover genomic characteristics that define testicular germ cell cancer

Testicular germ cell cancer, a disease that is rare but growing in incidence in men in the United States, is considered to be among the most curable of solid tumors. Now researchers from the University of North Carolina Lineberger Comprehensive Cancer Center and a consortium of institutions have discovered the genetic and genomic characteristics that define the disease.

12 Jun 2018

Research identifies new genetic variations that could indicate higher prostate cancer risk

As the result of a six-year long research process, Fredrick R. Schumacher, PhD, a cancer epidemiology researcher at Case Western Reserve University School of Medicine, and an international team of more than 100 colleagues have identified 63 new genetic variations that could indicate higher risk of prostate cancer in men of European descent.

12 Jun 2018

New blood test better than having a needle inserted into the eye

People diagnosed with a deadly form of cancer will no longer face the prospect of having a needle inserted into their eye thanks to a new blood test developed by Edith Cowan University researchers.

12 Jun 2018

High-sensitive troponin T detects more cardiac infarctions than conventional ones, shows study

Five percent more cardiac infarctions detected and 11 percent fewer patients suffering a relapse. That is the result of a study of more than 80,000 patients in which two cardiac damage markers were compared with each other.

8 Jun 2018

Classifying heart failure patients based on redox status may help personalize treatment

For more than six decades, oxidative stress has been linked to heart failure, a progressive weakening of the heart muscle that can lead to death. While antioxidant supplements such as vitamin C, vitamin B and beta-carotene have been widely used in heart failure, they often prove ineffective.

6 Jun 2018

Patients diagnosed with high-sensitivity troponin test have lower risk of future heart attack

The newer high-sensitivity troponin test discovers smaller amounts of heart-specific proteins, troponins, than the older troponin test and thus identifies more myocardial infarction patients than before.

5 Jun 2018

More follow-up testing may not help colorectal cancer patients, shows study

Logically, it would seem that more follow-up testing of cancer patients must be better than less - but this is not the case for patients who undergo surgery for colorectal cancer.

5 Jun 2018

Free-floating DNA analysis test may help detect early-stage lung cancer

A test that analyzes free-floating DNA in the blood may be able to detect early-stage lung cancer, a preliminary report from the ongoing Circulating Cell-Free Genome Atlas study suggests.

4 Jun 2018

Screening preemies for microRNA biomarkers may allow early intervention of cerebral palsy

As the first step toward predicting cerebral palsy in premature infants, scientists have identified a panel of microRNAs that are changed in babies who later develop abnormal muscle tone.

1 Jun 2018

New ACS guidelines recommend early screening for colorectal cancer

New guidelines developed by the American Cancer Society recommend that screening for colorectal cancer for average-risk adults begin at age 45, five years earlier than the previous recommendation.

1 Jun 2018

American Cancer Society releases updated guideline for CRC screening

An updated American Cancer Society guideline says colorectal cancer screening should begin at age 45 for people at average risk, based in part on data showing rates of colorectal cancer are increasing in young and middle-aged populations.

30 May 2018

Combining football with dietary guidance helps improve fitness, health in older prediabetics

Twice-weekly football training combined with dietary guidance improves fitness level and cardiovascular health profile in untrained 55-70-year-old women and men with prediabetes. Also leads to healthier weight loss than through normal dieting.

29 May 2018

Genomic medicine may redefine cardiovascular care in future, shows study

A new scientific statement from the American Heart Association summarizes the state-of-the-science of genomic medicine -- the study of the health effects of the molecular interactions of a person's unique genes -- for studying cardiovascular traits and disorders and for therapeutic screening.

29 May 2018

Blood Test News and Research

Nightingale Health to analyze biomarker profiles of 500,000 blood samples from UK Biobank

New guidelines recommend newborns with Down’s syndrome to receive leukemia test

Follow-up study confirms success of physiological test for autism

Single blood sample can provide adequate confirmation of diabetes

Novel chip can be used to identify rhinovirus strains as cause of asthma

Technology breakthrough could enable detection of fetal genetic abnormalities in early pregnancy

Researchers link red meat sensitivity spread by ticks with heart disease

Researchers discover genomic characteristics that define testicular germ cell cancer

Research identifies new genetic variations that could indicate higher prostate cancer risk

New blood test better than having a needle inserted into the eye

High-sensitive troponin T detects more cardiac infarctions than conventional ones, shows study

Classifying heart failure patients based on redox status may help personalize treatment

Patients diagnosed with high-sensitivity troponin test have lower risk of future heart attack

More follow-up testing may not help colorectal cancer patients, shows study

Free-floating DNA analysis test may help detect early-stage lung cancer

Screening preemies for microRNA biomarkers may allow early intervention of cerebral palsy

New ACS guidelines recommend early screening for colorectal cancer

American Cancer Society releases updated guideline for CRC screening

Combining football with dietary guidance helps improve fitness, health in older prediabetics

Genomic medicine may redefine cardiovascular care in future, shows study

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

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