Article
A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.
Arteriosclerosis, thrombosis, and vascular biology - 1 Sept 2014
Kyriakou Theodosios, Seedorf Udo, Goel Anuj, Hopewell Jemma C, Clarke Robert, Watkins Hugh, Farrall Martin
Abstract excerpt
OBJECTIVE: Increased levels of lipoprotein(a) are a highly heritable risk factor for coronary artery disease (CAD). The genetic determinants of lipoprotein(a) levels are mainly because of genetic variation in the apolipoprotein(a) gene (LPA). We have tested the association of a relatively common null allele of LPA with lipoprotein(a) levels and CAD risk in a large case-control cohort. We have also examined how...
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