首页> 外文期刊>The New England journal of medicine >Genomewide association analysis of coronary artery disease.
【24h】

Genomewide association analysis of coronary artery disease.

机译:全基因组关联分析的冠状动脉疾病。

获取原文
获取原文并翻译 | 示例

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.
机译:背景:现代基因分型平台允许系统搜索复杂疾病的遗传成分。我们进行了两项全基因组冠状动脉疾病关联研究的联合分析。方法:我们首先在Wellcome Trust病例对照协会(WTCCC)研究中鉴定了与冠状动脉疾病密切相关的染色体基因座(该研究涉及1926例冠状动脉疾病病例和2938例对照),并在德国MI中寻找复制基因。 [梗塞]家庭研究(涉及875例患有心肌梗塞的病例和1644名对照)。然后将两项研究中与冠状动脉疾病显着相关的其他单核苷酸多态性(SNP)数据(P <0.001)组合起来,以鉴定出具有高度真实关联可能性的其他基因座。两项研究中的基因分型都是使用GeneChip Human Mapping 500K Array Set(Affymetrix)进行的。结果:在WTCCC和德国研究中,在数千个染色体基因座中,同一基因座与冠状动脉疾病的关联最强:9p21.3号染色体(SNP,rs1333049)(P = 1.80x10(-14)和P =分别为3.40x10(-6)。总体而言,WTCCC研究发现与冠心病密切相关的9个基因座(P <1.2x10(-5),且假阳性的机率低于50%)。除了9p21.3染色体外,在德国研究中还成功复制了两个这样的基因座(调整P <0.05):染色体6q25.1(rs6922269)和染色体2q36.3(rs2943634)。两项研究的综合分析确定了另外四个与冠状动脉疾病显着相关的位点(P <1.3x10(-6))和真正关联的可能性很高(> 80%):1p13.3染色体(rs599839),1q41 (rs17465637),10q11.21(rs501120)和15q22.33(rs17228212)。结论:我们确定了几个遗传位点,这些基因位点单独或总体上显着影响了冠心病发展的风险。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号