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Title: Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
Authors: Talmud, PJ
Drenos, F
Shah, S
Shah, T
Palmen, J
Verzilli, C
Gaunt, TR
Pallas, J
Lovering, R
Li, K
Casas, JP
Sofat, R
Kumari, M
Rodriguez, S
Johnson, T
Newhouse, SJ
Dominiczak, A
Samani, NJ
Caulfield, M
Sever, P
Stanton, A
Shields, DC
Padmanabhan, S
Melander, O
Hastie, C
Delles, C
Ebrahim, S
Marmot, MG
Smith, GD
Lawlor, DA
Munroe, PB
Day, IN
Kivimaki, M
Whittaker, J
Humphries, SE
Hingorani, AD
ASCOT, investigators
NORDIL, investigators
BRIGHT, Consortium
First Published: Nov-2009
Citation: AM J HUM GENET, 2009, 85 (5), pp. 628-642
Abstract: Blood lipids are important cardiovascular disease (CVD) risk factors with both genetic and environmental determinants. The Whitehall II study (n=5592) was genotyped with the gene-centric HumanCVD BeadChip (Illumina). We identified 195 SNPs in 16 genes/regions associated with 3 major lipid fractions and 2 apolipoprotein components at p<10(-5), with the associations being broadly concordant with prior genome-wide analysis. SNPs associated with LDL cholesterol and apolipoprotein B were located in LDLR, PCSK9, APOB, CELSR2, HMGCR, CETP, the TOMM40-APOE-C1-C2-C4 cluster, and the APOA5-A4-C3-A1 cluster; SNPs associated with HDL cholesterol and apolipoprotein AI were in CETP, LPL, LIPC, APOA5-A4-C3-A1, and ABCA1; and SNPs associated with triglycerides in GCKR, BAZ1B, MLXIPL, LPL, and APOA5-A4-C3-A1. For 48 SNPs in previously unreported loci that were significant at p<10(-4) in Whitehall II, in silico analysis including the British Women's Heart and Health Study, BRIGHT, ASCOT, and NORDIL studies (total n>12,500) revealed previously unreported associations of SH2B3 (p<2.2x10(-6)), BMPR2 (p<2.3x10(-7)), BCL3/PVRL2 (flanking APOE; p<4.4x10(-8)), and SMARCA4 (flanking LDLR; p<2.5x10(-7)) with LDL cholesterol. Common alleles in these genes explained 6.1%-14.7% of the variance in the five lipid-related traits, and individuals at opposite tails of the additive allele score exhibited substantial differences in trait levels (e.g., >1 mmol/L in LDL cholesterol [approximately 1 SD of the trait distribution]). These data suggest that multiple common alleles of small effect can make important contributions to individual differences in blood lipids potentially relevant to the assessment of CVD risk. These genes provide further insights into lipid metabolism and the likely effects of modifying the encoded targets therapeutically.
DOI Link: 10.1016/j.ajhg.2009.10.014
eISSN: 1537-6605
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences

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