Association between endothelial nitric oxide synthase gene polymorphism (T-786C) and ischemic stroke susceptibility: a meta-analysis

被引:9
|
作者
Liu, Ruozhuo [1 ]
Geng, Peiliang [2 ,3 ]
Ma, Minghui [4 ]
Yu, Shengyuan [1 ]
Wang, Xiaolin [1 ]
Zhang, Wei [1 ]
Di, Hai [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Neurol, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Div Internal Med, Ctr Canc, Key Lab Oncol, Beijing 100853, Peoples R China
[3] Chinese PLA Med Sch, Beijing, Peoples R China
[4] Acad Mil Med Sci, Med Lib Chinese PLA, Minist Resource Construct, Beijing, Peoples R China
关键词
endothelial nitric oxide synthase; T-786C polymorphism; ischemic stroke; meta-analysis; NOS3; GENE; GLU/ASP POLYMORPHISM; REPEAT POLYMORPHISM; RISK; G894T; HAPLOTYPES; GLU298ASP;
D O I
10.3109/00207454.2013.873978
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: The endothelial nitric oxide synthase (eNOS) T-786C polymorphism has been implicated in a number of studies investigating ischemic stroke (IS), yet previously published studies showed inconsistent results that recent meta-analyses have not resolved. Methods: In the comprehensive meta-analysis of 12 association studies involving 2836 IS cases and 3354 control subjects, we used a more stringent inclusion method and summarized data on the association of eNOS T-786C polymorphism and IS susceptibility. Results: We found a significantly lowered IS risk under the CC vs. TT genetic model (odds ratio, OR = 0.53, 95% confidence interval, CI = 0.29-0.98, p = 0.160, I-2 = 45.5%) by random effects model in Caucasians and under the allele model C vs. T (OR = 0.42, 95% CI = 0.21-0.87) by fixed effects model in African-Americans. In addition, a significant increased risk of IS was observed in Asians (C vs. T: OR = 1.14, 95% CI = 1.02-1.28, p = 0.990, I-2 = 0.0%) by fixed effects model. Stratified analysis by mean age also showed that the allele C carriers, compared with the allele T allele carriers, had higher risk of suffering IS (OR = 1.16, 95% CI = 1.03-1.31) in the population of 60-65 years without heterogeneity. Conclusions: The combined results suggest that eNOS T-786C polymorphism may be associated with IS susceptibility among the population between 60 and 65 years in particular.
引用
收藏
页码:642 / 651
页数:10
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