Coronary artery disease (CAD) is a complex condition resulting from the interplay of behavioral, environmental, and genetic factors. While modifiable risk factors like smoking and hypertension are well-recognized, recent large-scale genomic studies have identified hundreds of genetic variants that significantly influence susceptibility. This inherited basis manifests in two primary forms: rare monogenic variants with large effects (such as familial hypercholesterolemia) and a broad polygenic architecture composed of common variants with small individual effects.
The integration of polygenic risk scores (PRS) into clinical practice offers a mechanism to refine risk prediction, particularly for younger individuals and those with intermediate clinical risk. Furthermore, genetic insights have validated several contemporary therapeutic targets and prioritized new pathways for drug development. Despite these advances, challenges remain regarding the standardization of genetic scores, equitable access across diverse ancestries, and the determination of cost-effectiveness in routine clinical implementation.
If you have following burning questions, then this podcast is worth listening.
1/ What is the importance of genetics in CAD ?
2/ If family history of CAD is negative, does it confers safety to the offsprings ?
3/ Can we diagnose the risk of future CAD at birth by genetic tests ?
4/ If the genetic risk of CAD is high, can we modify it by lifestyle changes ?
5/ Are there medicines to affect genetic susceptibility for CAD ?
This podcast is based on the latest article " The Inherited Basis of Coronary Artery Disease" by Dr Pradeep Natarajan etal Center for Genomic Medicine and Cardiovascular Research Center, Massachusetts General Hospital, Boston. Published in NEJM.
N Engl J Med 2026;394:576-87.
DOI: 10.1056/NEJMra2405153