Newly identified loci that influence lipid concentrations and risk of coronary artery disease
β Scribed by Willer, Cristen J; Sanna, Serena; Jackson, Anne U; Scuteri, Angelo; Bonnycastle, Lori L; Clarke, Robert; Heath, Simon C; Timpson, Nicholas J; Najjar, Samer S; Stringham, Heather M
- Book ID
- 109914710
- Publisher
- Nature Publishing Group
- Year
- 2008
- Tongue
- English
- Weight
- 422 KB
- Volume
- 40
- Category
- Article
- ISSN
- 1061-4036
- DOI
- 10.1038/ng.76
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β¦ Synopsis
To identify genetic variants influencing plasma lipid concentrations, we first used genotype imputation and meta-analysis to combine three genome-wide scans totaling 8,816 individuals and comprising 6,068 individuals specific to our study (1,874 individuals from the FUSION study of type 2 diabetes and 4,184 individuals from the SardiNIA study of aging-associated variables) and 2,758 individuals from the Diabetes Genetics Initiative, reported in a companion study in this issue. We subsequently examined promising signals in 11,569 additional individuals. Overall, we identify strongly associated variants in eleven loci previously implicated in lipid metabolism (ABCA1, the APOA5-APOA4-APOC3-APOA1 and APOE-APOC clusters, APOB, CETP, GCKR, LDLR, LPL, LIPC, LIPG and PCSK9) and also in several newly identified loci (near MVK-MMAB and GALNT2, with variants primarily associated with high-density lipoprotein (HDL) cholesterol; near SORT1, with variants primarily associated with low-density lipoprotein (LDL) cholesterol; near TRIB1, MLXIPL and ANGPTL3, with variants primarily associated with triglycerides; and a locus encompassing several genes near NCAN, with variants strongly associated with both triglycerides and LDL cholesterol). Notably, the 11 independent variants associated with increased LDL cholesterol concentrations in our study also showed increased frequency in a sample of coronary artery disease cases versus controls.Coronary artery disease (CAD) and stroke are the leading causes of morbidity, mortality and disability in industrialized countries, and the prevalence of these diseases is increasing rapidly in developing countries 1 . A main underlying pathology is atherosclerosis, a process of cumulative deposition of LDL cholesterol in the arteries supplying blood to the heart and brain that eventually leads to impaired or absent blood supply and myocardial infarction or stroke 1 . Consistent and compelling evidence has demonstrated association between lipoprotein-associated lipid concentrations and cardiovascular disease incidence worldwide 2-4 . Whereas high concentrations of LDL
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## Abstract Recently, genome wide association studies (GWAS) have identified a number of single nucleotide polymorphisms (SNPs) as being associated with coronary heart disease (CHD). We estimated the effect of these SNPs on incident CHD, stroke and total mortality in the prospective cohorts of the