<p>The SEA study is a genome-wide association study to identify genetic variants associated with premature atherosclerosis in  subjects included in the Pathobiological Determinants of Atherosclerosis in Youth (PDAY) repository - a unique NHLBI resource  including data, DNA and arterial specimens from over 3000 multi-ethnic subjects 15-34 years of age who died of non-atherosclerotic  causes (mostly trauma).  All PDAY subjects had post-mortem quantitative assessment of raised atherosclerotic lesions in their aorta  and coronary arteries - making this the largest and most carefully phenotyped cohort for premature atherosclerosis in the world.  The goal of the current project was to use the quantitative measure of raised atherosclerotic lesions in the PDAY cohort as the  target phenotype for a genome-wide association study and to use quantitative measures of subclinical atherosclerosis (coronary  calcium and carotid IMT) in the Multi-Ethnic Study of Atherosclerosis (MESA) to confirm or refute candidate loci identified from  the PDAY analysis.  Identifying genetic factors that predispose individuals to premature atherosclerosis could lead to more  effective screening and early treatment of high risk individuals and suggest novel molecular targets for treatment and prevention  interventions.</p>

SNPs and Extent of Atherosclerosis (SEA) Study

Atherosclerosis study with SNP Genotypes (Array) data on BDC (1,068 participants)

SNPs and Extent of Atherosclerosis (SEA) Study

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Summary