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
National Heart, Lung, and Blood Institute's Framingham Heart Study, Framingham, MA, USA.
Circ Cardiovasc Genet. 2011 Oct;4(5):557-64. doi: 10.1161/CIRCGENETICS.110.959197. Epub 2011 Aug 16.
The genetic background of atrial fibrillation (AF) in whites and African Americans is largely unknown. Genes in cardiovascular pathways have not been systematically investigated.
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).
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.
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。
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)。
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。