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在白人和非裔美国人中进行的大规模候选基因分析确定了与心房颤动相关的白细胞介素6受体多态性:美国国立心肺血液研究所的候选基因关联资源(CARe)项目。

Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project.

作者信息

Schnabel Renate B, Kerr Kathleen F, Lubitz Steven A, Alkylbekova Ermeg L, Marcus Gregory M, Sinner Moritz F, Magnani Jared W, Wolf Philip A, Deo Rajat, Lloyd-Jones Donald M, Lunetta Kathryn L, Mehra Reena, Levy Daniel, Fox Ervin R, Arking Dan E, Mosley Thomas H, Müller-Nurasyid Martina, Young Taylor R, Wichmann H-Erich, Seshadri Sudha, Farlow Deborah N, Rotter Jerome I, Soliman Elsayed Z, Glazer Nicole L, Wilson James G, Breteler Monique M B, Sotoodehnia Nona, Newton-Cheh Christopher, Kääb Stefan, Ellinor Patrick T, Alonso Alvaro, Benjamin Emelia J, Heckbert Susan R

机构信息

National Heart, Lung, and Blood Institute's Framingham Heart Study, Framingham, MA, USA.

出版信息

Circ Cardiovasc Genet. 2011 Oct;4(5):557-64. doi: 10.1161/CIRCGENETICS.110.959197. Epub 2011 Aug 16.

Abstract

BACKGROUND

The genetic background of atrial fibrillation (AF) in whites and African Americans is largely unknown. Genes in cardiovascular pathways have not been systematically investigated.

METHODS AND RESULTS

We examined a panel of approximately 50,000 common single-nucleotide polymorphisms (SNPs) in 2095 cardiovascular candidate genes and AF in 3 cohorts with participants of European (n=18,524; 2260 cases) or African American descent (n=3662; 263 cases) in the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource. Results in whites were followed up in the German Competence Network for AF (n=906, 468 cases). The top result was assessed in relation to incident ischemic stroke in the Cohorts for Heart and Aging Research in Genomic Epidemiology Stroke Consortium (n=19,602 whites, 1544 incident strokes). SNP rs4845625 in the IL6R gene was associated with AF (relative risk [RR] C allele, 0.90; 95% confidence interval [CI], 0.85-0.95; P=0.0005) in whites but did not reach statistical significance in African Americans (RR, 0.86; 95% CI, 0.72-1.03; P=0.09). The results were comparable in the German AF Network replication, (RR, 0.71; 95% CI, 0.57-0.89; P=0.003). No association between rs4845625 and stroke was observed in whites. The known chromosome 4 locus near PITX2 in whites also was associated with AF in African Americans (rs4611994; hazard ratio, 1.40; 95% CI, 1.16-1.69; P=0.0005).

CONCLUSIONS

In a community-based cohort meta-analysis, we identified genetic association in IL6R with AF in whites. Additionally, we demonstrated that the chromosome 4 locus known from recent genome-wide association studies in whites is associated with AF in African Americans.

摘要

背景

白人和非裔美国人房颤(AF)的遗传背景很大程度上未知。心血管通路中的基因尚未得到系统研究。

方法与结果

我们在国家心肺血液研究所的候选基因关联资源中,对2095个心血管候选基因中的约50000个常见单核苷酸多态性(SNP)以及3个队列中的房颤进行了检测,这些队列的参与者有欧洲血统(n = 18524;2260例病例)或非裔美国血统(n = 3662;263例病例)。白人中的结果在德国房颤能力网络中进行了随访(n = 906,468例病例)。在基因组流行病学中风联盟的心脏与衰老研究队列中,对与缺血性卒中事件相关的最高结果进行了评估(n = 19602名白人,1544例缺血性卒中事件)。白细胞介素6受体(IL6R)基因中的SNP rs4845625与白人的房颤相关(相对风险[RR] C等位基因,0.90;95%置信区间[CI],0.85 - 0.95;P = 0.0005),但在非裔美国人中未达到统计学显著性(RR,0.86;95% CI,0.72 - 1.03;P = 0.09)。在德国房颤网络重复研究中的结果具有可比性(RR,0.71;95% CI,0.57 - 0.89;P = 0.003)。在白人中未观察到rs4845625与卒中之间的关联。白人中已知的位于PITX2附近的4号染色体位点在非裔美国人中也与房颤相关(rs4611994;风险比,1.40;95% CI,1.16 - 1.69;P = 0.0005)。

结论

在一项基于社区队列的荟萃分析中,我们确定了白细胞介素6受体基因与白人房颤的遗传关联。此外,我们证明了在白人近期全基因组关联研究中已知的4号染色体位点与非裔美国人的房颤相关。

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