Tsai Chia-Ti, Chang Sheng-Nan, Chang Shu-Hsuan, Lee Jen-Kuang, Lin Lian-Yu, Wu Cho-Kai, Yu Chih-Chieh, Wang Yi-Chih, Tseng Chuen-Den, Lai Ling-Ping, Hwang Juey-Jen, Chiang Fu-Tien, Lin Jiunn-Lee
Division of Cardiology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan; Department of Internal Medicine, National Taiwan University Hospital Yun-Lin Branch, Yun-Lin, Taiwan.
Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan; Department of Internal Medicine, National Taiwan University Hospital Yun-Lin Branch, Yun-Lin, Taiwan.
Heart Rhythm. 2014 Aug;11(8):1384-90. doi: 10.1016/j.hrthm.2014.04.014. Epub 2014 Apr 13.
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.
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.
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.
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).
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.
关于基因多态性对心房颤动(AF)患者中风风险的影响,现有证据较少。血管紧张素II在促血栓形成的心房内膜重塑中起病理生理作用。
本研究旨在调查肾素-血管紧张素系统基因多态性对AF患者前瞻性队列中风发生率的影响。
对712例AF患者进行了为期10.3±2.7年的纵向随访。对肾素-血管紧张素系统基因的8种多态性进行了基因分型。
携带血管紧张素原基因启动子中与较高启动子活性相关的G-6等位基因的患者比非携带者更易发生中风(风险比2.54,95%置信区间[1.26-5.12],校正CHADS2评分后P=0.009)。G-6A多态性在中风风险预测方面提供了CHADS2评分之外的额外信息(C统计量0.672对0.724,P=0.039)。在单倍型分析中,包含-217G/-6G且与最高启动子活性相关的血管紧张素原基因启动子单倍型与中风风险增加相关(P=0.004)。G-217/G-6单倍型携带者比非携带者更易发生中风(风险比2.78,95%置信区间1.37-5.64,多变量调整后P=0.003)。在药物遗传学分析中,携带G-6的受试者中风风险增加可通过同时使用血管紧张素转换酶抑制剂或血管紧张素II受体阻滞剂治疗而消除(交互作用P=0.012)。
除CHADS2评分外,血管紧张素原基因多态性可被视为AF患者中风的额外遗传预测指标。血管紧张素原基因分型有助于确定哪些AF患者可能从血管紧张素转换酶抑制剂或血管紧张素II受体阻滞剂治疗中获益。