Ma Qiong, Lv Jianmin, Huang Kuikui, Guo Huaqi, Yang Wenliang, Luo Wen, Qiu Jie, Yang Lan
Department of Maternal, Child and Adolescent Health, School of Public Health, Lanzhou University, Gansu, China.
Gansu Provincial Maternity and Child Care Hospital, Gansu, China.
Hypertens Res. 2016 Dec;39(12):899-906. doi: 10.1038/hr.2016.95. Epub 2016 Jul 28.
Recent studies have reported the association between endothelial nitric oxide synthase (eNOS) gene G894T polymorphism and pregnancy-induced hypertension (PIH). However, the results have been inconsistent. We conducted a comprehensive meta-analysis to explore this association. A total of 36 case-control studies involving 4028 PIH cases and 7672 controls were ultimately included. In the overall analysis, no association was identified between eNOS gene G894T polymorphism and PIH risk in any of the genetic models. In the subgroup analysis, the results showed that T-allele carriers had a higher risk of PIH than those with the G allele in Asians (G vs. T: odds ratio (OR)=0.76, 95% confidence interval (CI)=0.63-0.91, P=0.002; GT+TT vs. GG: OR=1.32, 95% CI=1.09-1.59, P=0.004; TT vs. GT+GG: OR=1.96, 95% CI=1.26-3.06, P=0.003; TT vs. GG: OR=1.99, 95% CI=1.27-3.11, P=0.003; GT vs. GG: OR=1.23, 95% CI=1.05-1.43, P=0.009). For Latin American and African populations, the association between G894T polymorphism and susceptibility to PIH was only observed in the dominant model. However, no association was observed in Europeans and Americans. Therefore, eNOS gene G894T polymorphism was related to PIH risk, especially for Asians.
近期研究报道了内皮型一氧化氮合酶(eNOS)基因G894T多态性与妊娠期高血压疾病(PIH)之间的关联。然而,结果并不一致。我们进行了一项全面的荟萃分析以探究这种关联。最终纳入了36项病例对照研究,涉及4028例PIH病例和7672例对照。在总体分析中,在任何遗传模型中均未发现eNOS基因G894T多态性与PIH风险之间存在关联。在亚组分析中,结果显示,在亚洲人群中,T等位基因携带者患PIH的风险高于携带G等位基因者(G vs. T:比值比(OR)=0.76,95%置信区间(CI)=0.63 - 0.91,P = 0.002;GT + TT vs. GG:OR = 1.32,95% CI = 1.09 - 1.59,P = 0.004;TT vs. GT + GG:OR = 1.96,95% CI = 1.26 - 3.06,P = 0.003;TT vs. GG:OR = 1.99, 95% CI = 1.27 - 3.11,P = 0.003;GT vs. GG:OR = 1.23,95% CI = 1.05 - 1.43, P = 0.009)。对于拉丁美洲和非洲人群,仅在显性模型中观察到G894T多态性与PIH易感性之间的关联。然而,在欧洲人和美国人中未观察到关联。因此,eNOS基因G894T多态性与PIH风险相关,尤其是在亚洲人群中。