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Renin-angiotensin system gene polymorphisms predict the risk of stroke in patients with atrial fibrillation: A 10-year prospective follow-up study

机译:肾素 - 血管紧张素系统基因多态性预测心房颤动患者中风的风险:一项为期10年的前瞻性随访研究

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Background Little evidence is available regarding the impact of genetic polymorphisms on the risk of stroke in patients with atrial fibrillation (AF). Angiotensin II plays a pathophysiologic role in prothrombotic atrial endocardial remodeling. Objective The purpose of this study was to investigate the effect of polymorphisms of renin-angiotensin system genes on the incidence of stroke in a prospective cohort of patients with AF. Methods A total of 712 AF patients were longitudinally followed-up for 10.3 ± 2.7 years. Eight polymorphisms of renin-angiotensin system genes were genotyped. Results Patients carrying the G-6 allele in the promoter of the angiotensinogen gene, which was associated with higher promoter activity, were more likely to develop stroke than were noncarriers (hazard ratio 2.54, 95% confidence interval [1.26-5.12], P =.009 after adjustment for CHADS2 score). G-6A polymorphism provides information additional to CHADS2 on stroke risk prediction (C-statistic 0.672 vs 0.724, P =.039). In haplotype analysis, angiotensinogen gene promoter haplotypes containing -217G/-6G, which was associated with the highest promoter activity, were associated with an increased risk of stroke (P =.004). G-217/G-6 haplotype carriers were even more likely to develop stroke than were noncarriers (hazard ratio 2.78, 95% confidence interval 1.37-5.64, P =.003 after multivariable adjustment). In pharmacogenetic analysis, the increased risk of stroke in subjects carrying G-6 was eliminated by concomitant treatment with an angiotensin-converting enzyme inhibitor or angiotensin II receptor blocker (P =.012 for interaction). Conclusion In addition to the CHADS2 score, angiotensinogen gene polymorphisms may be considered an additional genetic predictor of stroke in patients with AF. Genotyping of the angiotensinogen gene is helpful to determine which AF patients may benefit from treatment with an angiotensin-converting enzyme inhibitor or angiotensin II receptor blocker.
机译:背景几乎没有证据表明遗传多态性对心房颤动患者中风风险的影响(AF)。血管紧张素II在促血栓性心房内膜重塑中起病理生理作用。目的,这项研究的目的是研究肾素 - 血管紧张素系统基因多态性对AF患者的前瞻性队列中中风发生率的影响。方法总共有712名AF患者进行纵向跟踪10。3±2。7年。基因分型肾素 - 血管紧张素系统基因的八种多态性。与非载体相比,与较高的启动子活性相关的血管紧张素基因启动子中携带G-6等位基因的患者比非载体更有可能发展中风(危险比2.54,95%置信区间[1.26-5.12],p = .009在调整CHADS2分数之后)。 G-6A多态性提供了有关中风风险预测的乍得2号信息(C统计0.672 vs 0.724,p = .039)。在单倍型分析中,含有-217G/-6G的血管紧张素基因基因启动子单倍型与最高启动子活性有关,与中风风险增加有关(p = .004)。 G-217/G-6单倍型载体比非驾驶员更有可能发生中风(危险比2.78,95%置信区间1.37-5.64,多变量调整后P = .003)。在药物遗传学分析中,通过与血管紧张素转换酶抑制剂或血管紧张素II受体阻滞剂的同时治疗消除了携带G-6受试者中风的风险增加(相互作用的P = .012)。结论除了CHADS2评分外,血管紧张素基因的多态性可能被认为是AF患者中风的附加遗传预测因子。血管紧张素基因基因的基因分型有助于确定哪些AF患者可以通过血管紧张素转换酶抑制剂或血管紧张素II受体阻滞剂受益。

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