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Circ Cardiovasc Genet. 2011 Oct;4(5):557-64. doi: 10.1161/CIRCGENETICS.110.959197. Epub 2011 Aug 16.
2
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本文引用的文献

1
European ancestry as a risk factor for atrial fibrillation in African Americans.欧洲血统是非洲裔美国人发生房颤的一个危险因素。
Circulation. 2010 Nov 16;122(20):2009-15. doi: 10.1161/CIRCULATIONAHA.110.958306.
2
Validation of an atrial fibrillation risk algorithm in whites and African Americans.心房颤动风险算法在白人和非裔美国人中的验证。
Arch Intern Med. 2010 Nov 22;170(21):1909-17. doi: 10.1001/archinternmed.2010.434.
3
The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology.与心房颤动易感性相关的 4q25 变异与中风的关联仅限于心源性栓塞性中风。
Stroke. 2010 Sep;41(9):1850-7. doi: 10.1161/STROKEAHA.110.587980. Epub 2010 Jul 29.
4
Candidate gene association resource (CARe): design, methods, and proof of concept.候选基因关联资源(CARe):设计、方法及概念验证
Circ Cardiovasc Genet. 2010 Jun;3(3):267-75. doi: 10.1161/CIRCGENETICS.109.882696. Epub 2010 Apr 17.
5
Common variants in KCNN3 are associated with lone atrial fibrillation.常见的 KCNN3 变体与孤立性心房颤动有关。
Nat Genet. 2010 Mar;42(3):240-4. doi: 10.1038/ng.537. Epub 2010 Feb 21.
6
The relation of genetic and environmental factors to systemic inflammatory biomarker concentrations.遗传和环境因素与全身炎症生物标志物浓度的关系。
Circ Cardiovasc Genet. 2009 Jun;2(3):229-37. doi: 10.1161/CIRCGENETICS.108.804245. Epub 2009 Mar 31.
7
Intracardiac and extracardiac markers of inflammation during atrial fibrillation.心房颤动期间的心脏内和心脏外炎症标志物。
Heart Rhythm. 2010;7(2):149-54. doi: 10.1016/j.hrthm.2009.10.004. Epub 2009 Oct 12.
8
Myocardin is required for cardiomyocyte survival and maintenance of heart function.心肌素是心肌细胞存活和心脏功能维持所必需的。
Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18734-9. doi: 10.1073/pnas.0910749106. Epub 2009 Oct 22.
9
Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation.增强的钾电流是与家族性心房颤动相关的两种遗传缺陷的共同表型。
J Mol Cell Cardiol. 2010 Jan;48(1):181-90. doi: 10.1016/j.yjmcc.2009.07.020. Epub 2009 Jul 30.
10
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.在欧洲血统个体中,ZFHX3基因的变异与心房颤动有关。
Nat Genet. 2009 Aug;41(8):879-81. doi: 10.1038/ng.416. Epub 2009 Jul 13.

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.

DOI:10.1161/CIRCGENETICS.110.959197
PMID:21846873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3224824/
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。