共 36 条
GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease
被引:52
作者:

Aouizerat, Bradley E.
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机构:
Univ Calif San Francisco, Inst Human Genet, Dept Physiol Nursing, San Francisco, CA 94143 USA Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA

Vittinghoff, Eric
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Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA

Musone, Stacy L.
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机构: Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA

Pawlikowska, Ludmila
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Univ Calif San Francisco, Inst Human Genet, Dept Anesthesia & Perioperat Care, San Francisco, CA 94143 USA Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA

Kwok, Pui-Yan
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Univ Calif San Francisco, Cardiovasc Res Inst, Inst Human Genet, San Francisco, CA 94143 USA Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA

Olgin, Jeffrey E.
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Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA

Tseng, Zian H.
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Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA
机构:
[1] Univ Calif San Francisco, Dept Med, Div Cardiol, Sect Cardiac Electrophysiol,Inst Human Genet, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Inst Human Genet, Dept Physiol Nursing, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Inst Human Genet, Dept Anesthesia & Perioperat Care, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Cardiovasc Res Inst, Inst Human Genet, San Francisco, CA 94143 USA
基金:
美国国家卫生研究院;
关键词:
NOS1 REGULATOR NOS1AP;
RISK-FACTOR;
DEATH;
POLYMORPHISMS;
VARIANT;
REPOLARIZATION;
FAMILIES;
PROTEIN;
HEART;
D O I:
10.1186/1471-2261-11-29
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: Epidemiologic evidence suggests a heritable component to risk for sudden cardiac arrest independent of risk for myocardial infarction. Recent candidate gene association studies for community sudden cardiac arrests have focused on a limited number of biological pathways and yielded conflicting results. We sought to identify novel gene associations for sudden cardiac arrest in patients with coronary artery disease by performing a genome-wide association study. Methods: Tagging SNPs (n = 338,328) spanning the genome were typed in a case-control study comparing 89 patients with coronary artery disease and sudden cardiac arrest due to ventricular tachycardia or ventricular fibrillation to 520 healthy controls. Results: Fourteen SNPs including 7 SNPs among 7 genes (ACYP2, AP1G2, ESR1, DGES2, GRIA1, KCTD1, ZNF385B) were associated with sudden cardiac arrest (all p < 1.30 x 10(-7)), following Bonferroni correction and adjustment for population substructure, age, and sex; genetic variation in ESR1 (p = 2.62 x 10(-8); Odds Ratio [OR] = 1.43, 95% confidence interval [CI]: 1.277, 1.596) has previously been established as a risk factor for cardiovascular disease. In tandem, the role of 9 genes for monogenic long QT syndrome (LQT1-9) was assessed, yielding evidence of association with CACNA1C (LQT8; p = 3.09 x 10(-4); OR = 1.18, 95% CI: 1.079, 1.290). We also assessed 4 recently published gene associations for sudden cardiac arrest, validating NOS1AP (p = 4.50 x 10(-2), OR = 1.15, 95% CI: 1.003, 1.326), CSMD2 (p = 6.6 x 10(-3), OR = 2.27, 95% CI: 1.681, 2.859), and AGTR1 (p = 3.00 x 10(-3), OR = 1.13, 95% CI: 1.042, 1.215). Conclusion: We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.
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