Association of genetic variants previously implicated in coronary artery disease with age at onset of coronary artery disease requiring revascularizations.

ABSTRACT:

Background

The relation between burden of risk factors, familial coronary artery disease (CAD), and known genetic variants underlying CAD and low-density lipoprotein cholesterol (LDL-C) levels is not well-explored in clinical samples. We aimed to investigate the association of these measures with age at onset of CAD requiring revascularizations in a clinical sample of patients undergoing first-time coronary angiography.

Methods

1599 individuals (mean age 64 years [min-max 29-96 years], 28% women) were genotyped (from blood drawn as part of usual clinical care) in the Copenhagen area (2010-2014). The burden of common genetic variants was measured as aggregated genetic risk scores (GRS) of single nucleotide polymorphisms (SNPs) discovered in genome-wide association studies.

SUBMITTER: Andersson C 

PROVIDER: S-EPMC6364925 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature