Genomewide association analysis of coronary artery disease

被引:1605
作者
Samani, Nilesh J. [1 ]
Erdmann, Jeanette
Hall, Alistair S.
Hengstenberg, Christian
Mangino, Massimo
Mayer, Bjoern
Dixon, Richard J.
Meitinger, Thomas
Braund, Peter
Wichmann, H.-Erich
Barrett, Jennifer H.
Koenig, Inke R.
Stevens, Suzanne E.
Szymczak, Silke
Tregouet, David-Alexandre
Iles, Mark M.
Pahlke, Friedrich
Pollard, Helen
Lieb, Wolfgang
Cambien, Francois
Fischer, Marcus
Ouwehand, Willem
Blankenberg, Stefan
Balmforth, Anthony J.
Baessler, Andrea
Ball, Stephen G.
Strom, Tim M.
Braenne, Ingrid
Gieger, Christian
Deloukas, Panos
Tobin, Martin D.
Ziegler, Andreas
Thompson, John R.
Schunkert, Heribert
机构
[1] Univ Leicester, Glenfield Gen Hosp, Dept Cardiovasc Sci, Leicester LE3 9QP, Leics, England
[2] Med Univ Lubeck, Med Klin 2, D-23538 Lubeck, Germany
[3] Univ Leeds, Leeds, W Yorkshire, England
[4] Univ Cambridge, Cambridge, England
[5] Wellcome Trust Sanger Inst, Hinxton, England
[6] Wellcome Trust Sanger Inst, Hinxton, England
[7] Univ Regensburg, D-8400 Regensburg, Germany
[8] GSF Forschungszentrum Umwelt & Gesundheit GMBH, Neuherberg, Germany
[9] Tech Univ Munich, D-8000 Munich, Germany
[10] Univ Munich, Munich, Germany
[11] Johannes Gutenberg Univ Mainz, D-6500 Mainz, Germany
[12] Univ Paris 06, INSERM, UMR S525, Paris, France
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1056/NEJMoa072366
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Modern genotyping platforms permit a systematic search for inherited components of complex diseases. We performed a joint analysis of two genomewide association studies of coronary artery disease. Methods We first identified chromosomal loci that were strongly associated with coronary artery disease in the Wellcome Trust Case Control Consortium (WTCCC) study (which involved 1926 case subjects with coronary artery disease and 2938 controls) and looked for replication in the German MI [Myocardial Infarction] Family Study (which involved 875 case subjects with myocardial infarction and 1644 controls). Data on other single-nucleotide polymorphisms (SNPs) that were significantly associated with coronary artery disease in either study (P<0.001) were then combined to identify additional loci with a high probability of true association. Genotyping in both studies was performed with the use of the GeneChip Human Mapping 500K Array Set (Affymetrix). Results Of thousands of chromosomal loci studied, the same locus had the strongest association with coronary artery disease in both the WTCCC and the German studies: chromosome 9p21.3 (SNP, rs1333049) (P=1.80x10(-14) and P=3.40x10(-6), respectively). Overall, the WTCCC study revealed nine loci that were strongly associated with coronary artery disease (P<1.2x10(-5) and less than a 50% chance of being falsely positive). In addition to chromosome 9p21.3, two of these loci were successfully replicated (adjusted P<0.05) in the German study: chromosome 6q25.1 (rs6922269) and chromosome 2q36.3 (rs2943634). The combined analysis of the two studies identified four additional loci significantly associated with coronary artery disease (P<1.3x10(-6)) and a high probability(>80%) of a true association: chromosomes 1p13.3 (rs599839), 1q41 (rs17465637), 10q11.21 (rs501120), and 15q22.33 (rs17228212). Conclusions We identified several genetic loci that, individually and in aggregate, substantially affect the risk of development of coronary artery disease.
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页码:443 / 453
页数:11
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