Genomewide association analysis of coronary artery disease

被引:1589
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
英国惠康基金; 英国医学研究理事会;
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.
引用
收藏
页码:443 / 453
页数:11
相关论文
共 32 条
  • [1] ALFAKIH K, IN PRESS ATHEROSCLER
  • [2] A haplotype map of the human genome
    Altshuler, D
    Brooks, LD
    Chakravarti, A
    Collins, FS
    Daly, MJ
    Donnelly, P
    Gibbs, RA
    Belmont, JW
    Boudreau, A
    Leal, SM
    Hardenbol, P
    Pasternak, S
    Wheeler, DA
    Willis, TD
    Yu, FL
    Yang, HM
    Zeng, CQ
    Gao, Y
    Hu, HR
    Hu, WT
    Li, CH
    Lin, W
    Liu, SQ
    Pan, H
    Tang, XL
    Wang, J
    Wang, W
    Yu, J
    Zhang, B
    Zhang, QR
    Zhao, HB
    Zhao, H
    Zhou, J
    Gabriel, SB
    Barry, R
    Blumenstiel, B
    Camargo, A
    Defelice, M
    Faggart, M
    Goyette, M
    Gupta, S
    Moore, J
    Nguyen, H
    Onofrio, RC
    Parkin, M
    Roy, J
    Stahl, E
    Winchester, E
    Ziaugra, L
    Shen, Y
    [J]. NATURE, 2005, 437 (7063) : 1299 - 1320
  • [3] Bosserhoff AK, 2002, HISTOL HISTOPATHOL, V17, P289, DOI 10.14670/HH-17.289
  • [4] A comprehensive linkage analysis for myocardial infarction and its related risk factors
    Broeckel, U
    Hengstenberg, C
    Mayer, B
    Holmer, S
    Martin, LJ
    Comuzzie, AG
    Blangero, J
    Nürnberg, P
    Reis, A
    Riegger, GAJ
    Jacob, HJ
    Schunkert, H
    [J]. NATURE GENETICS, 2002, 30 (02) : 210 - 214
  • [5] Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    Burton, Paul R.
    Clayton, David G.
    Cardon, Lon R.
    Craddock, Nick
    Deloukas, Panos
    Duncanson, Audrey
    Kwiatkowski, Dominic P.
    McCarthy, Mark I.
    Ouwehand, Willem H.
    Samani, Nilesh J.
    Todd, John A.
    Donnelly, Peter
    Barrett, Jeffrey C.
    Davison, Dan
    Easton, Doug
    Evans, David
    Leung, Hin-Tak
    Marchini, Jonathan L.
    Morris, Andrew P.
    Spencer, Chris C. A.
    Tobin, Martin D.
    Attwood, Antony P.
    Boorman, James P.
    Cant, Barbara
    Everson, Ursula
    Hussey, Judith M.
    Jolley, Jennifer D.
    Knight, Alexandra S.
    Koch, Kerstin
    Meech, Elizabeth
    Nutland, Sarah
    Prowse, Christopher V.
    Stevens, Helen E.
    Taylor, Niall C.
    Walters, Graham R.
    Walker, Neil M.
    Watkins, Nicholas A.
    Winzer, Thilo
    Jones, Richard W.
    McArdle, Wendy L.
    Ring, Susan M.
    Strachan, David P.
    Pembrey, Marcus
    Breen, Gerome
    St Clair, David
    Caesar, Sian
    Gordon-Smith, Katherine
    Jones, Lisa
    Fraser, Christine
    Green, Elain K.
    [J]. NATURE, 2007, 447 (7145) : 661 - 678
  • [6] Focus on research: What genome-wide association studies can do for medicine
    Christensen, Kaare
    Murray, Jeffrey C.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (11) : 1094 - 1097
  • [7] Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction
    Fischer, M
    Broeckel, U
    Holmer, S
    Baessler, A
    Hengstenberg, C
    Mayer, B
    Erdmann, J
    Klein, G
    Riegger, G
    Jacob, HJ
    Schunkert, H
    [J]. CIRCULATION, 2005, 111 (07) : 855 - 862
  • [8] New risk factors for atherosclerosis and patient risk assessment
    Fruchart, JC
    Nierman, MC
    Stroes, ESG
    Kastelein, JJP
    Duriez, P
    [J]. CIRCULATION, 2004, 109 (23) : 15 - 19
  • [9] P15(INK4B) IS A POTENTIAL EFFECTOR OF TGF-BETA-INDUCED CELL-CYCLE ARREST
    HANNON, GJ
    BEACH, D
    [J]. NATURE, 1994, 371 (6494) : 257 - 261
  • [10] A common variant on chromosome 9p21 affects the risk of myocardial infarction
    Helgadottir, Anna
    Thorleifsson, Gudmar
    Manolescu, Andrei
    Gretarsdottir, Solveig
    Blondal, Thorarinn
    Jonasdottir, Aslaug
    Jonasdottir, Adalbjorg
    Sigurdsson, Asgeir
    Baker, Adam
    Palsson, Arnar
    Masson, Gisli
    Gudbjartsson, Daniel F.
    Magnusson, Kristinn P.
    Andersen, Karl
    Levey, Allan I.
    Backman, Valgerdur M.
    Matthiasdottir, Sigurborg
    Jonsdottir, Thorbjorg
    Palsson, Stefan
    Einarsdottir, Helga
    Gunnarsdottir, Steinunn
    Gylfason, Arnaldur
    Vaccarino, Viola
    Hooper, W. Craig
    Reilly, Muredach P.
    Granger, Christopher B.
    Austin, Harland
    Rader, Daniel J.
    Shah, Svati H.
    Quyyumi, Arshed A.
    Gulcher, Jeffrey R.
    Thorgeirsson, Gudmundur
    Thorsteinsdottir, Unnur
    Kong, Augustine
    Stefansson, Kari
    [J]. SCIENCE, 2007, 316 (5830) : 1491 - 1493