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Genetics/Genomics News
Researchers develop prediction model for adverse cardiac events in mitochondrial diseases
Researchers have developed the first prediction model for the prediction of HF- and arrhythmia-related major adverse cardiac events in patients with mitochondrial diseases.
Rare genetic coding variants may predict high-risk SCAD phenotype
Approximately one in five adults with spontaneous coronary artery dissection with high-risk features had an increased burden of rare genetic variants on whole-exome sequencing, suggesting testing may be considered, researchers reported.
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Angiotensin receptor blockers, beta-blockers have separate, joint benefits in Marfan syndrome
Angiotensin receptor blockers and beta-blockers slow down the expansion of the aorta in patients with Marfan syndrome and no previous aortic surgery, according to data reported at the European Society of Cardiology Congress.
PRE-DETERMINE: Polygenic score predicts risk for sudden cardiac death in CAD
A validated genome-wide polygenic risk score predicted clinically meaningful absolute risk for sudden arrhythmic death in a cohort of patients with CAD without severe left ventricular dysfunction, researchers reported.
Combined monogenic, polygenic risk prediction spurs changes in CAD management
A combined monogenic and polygenic risk assessment for CAD can identify individuals at high inherited risk before overt manifestation of traditional risk factors, potentially improving clinician decision-making on preventive interventions.
No dementia, cognitive risk with PCSK9 inhibition; statin findings mixed
Data from a genetics-based study show PCSK9 inhibition does not affect cognition function or dementia risk; however, statin use may be associated with some impaired cognitive performance that is outweighed by any CV benefits.
Optimal CV health behaviors may mitigate genetic risk for stroke
Maintaining optimal CV health by following the American Heart Association’s Life’s Simple 7 protected people from stroke, even among those at high genetic risk, data from a long-term analysis show.
Unique cell, immune system ‘signatures’ may reveal causes of congenital heart disease
Researchers using RNA sequencing have identified unique cell and immune system signatures in tissue samples of children with congenital heart disease, offering a rare opportunity to better understand the origins of a complex disease.
Recommendations for genetic testing to prevent sudden cardiac death in athletes
Cardiologists should work with experienced centers performing genetic testing to identify and manage inherited cardiac conditions in young athletes and inform patients of risks and benefits, according to a new joint scientific statement.
Genetic HMG-CoA reductase inhibition may raise cataract risk
Genetic inhibition of HMG-CoA reductase, a state that mimics long-term statin use, was associated with greater risk for developing cataract compared with individuals without genetic inhibition, researchers reported.
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Headline News
Burnout, withdrawal remain ‘alarmingly high’ among physicians and residents
September 17, 20242 min read -
Headline News
Over one-third of adults not planning on receiving recommended vaccines this fall
September 18, 20242 min read -
Headline News
Popular home BP devices unable to provide accurate readings for millions due to sizing
September 19, 20242 min read