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Genetics/Genomics News
Some risk for non-syndromic congenital heart disease inherited from healthy parents
Researchers have discovered genetic evidence that some of the risk for non-syndromic congenital heart disease is inherited from healthy parents.
Study of genomics of antiplatelet therapy continues
The TAILOR-PCI study has received an additional $7 million from the National Heart, Lung and Blood Institute to complete research on whether prescribing antiplatelet therapy based on a patient’s CYP2C19 genotype will prevent MI, stroke, unstable angina and CV death in patients who undergo PCI.
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Genetic variants may account for paradoxical racial difference in AF risk
An atrial fibrillation–associated single nucleotide polymorphism, rs10824026, may partially be the cause of the paradoxical racial difference in risk for atrial fibrillation between white and black individuals, researchers reported in JAMA Cardiology.
Genetic score may improve CVD risk prediction in individuals at intermediate risk
Adding genetic risk score to phenotypic risk prediction of CVD added minimum benefit overall, but it may improve predictability in those at intermediate risk, according to data published in Heart.
Heterozygous familial hypercholesterolemia hastens risk for CHD
CHD onset in patients with high cholesterol levels caused by heterozygous familial hypercholesterolemia can be accelerated by decades, according to study data published in Circulation.
Genetic variants play role in clopidogrel effectiveness after minor stroke, TIA
In a subgroup analysis of the CHANCE trial, clopidogrel plus aspirin was only effective in reducing the risk for new stroke after minor stroke or transient ischemic attack in patients who were not carriers of CYP2C19 loss-of-function alleles.
Genetic testing helps identify causes of sudden cardiac death in children, young adults
The addition of genetic testing to the autopsy investigation may better identify possible causes of sudden cardiac death in children and young adults, according to data published in The New England Journal of Medicine.
Athletic participation risk appears acceptable in properly managed CPVT
Athletes with catecholaminergic polymorphic ventricular tachycardia, or CPVT, may safely compete if shared decision making and effective treatment are utilized, according to data published in JACC: Clinical Electrophysiology.
Genetic variant may elevate risk for acute kidney injury after cardiac surgery
A common genetic variant is associated with increased risk for acute kidney injury after cardiac surgery, recent findings indicate.
Researchers find genetic variant linked to reduced risk for CAD
Researchers reported in The New England Journal of Medicine that they have found a variant of the ASGR1 gene associated with reduced risk for CAD.
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Headline News
A potential new paradigm for treating acute migraine: Timolol nasal spray
November 15, 20245 min read -
Headline News
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November 15, 20242 min read -
Headline News
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