Department of Maternal and Child Health Care, School of Public Health, Shandong University, Jinan 250012, China.
Metabolism. 2013 Feb;62(2):196-203. doi: 10.1016/j.metabol.2012.07.008. Epub 2012 Sep 7.
A recent genome wide association study identified eight hypertension susceptibility loci in Europeans. Subsequently, several studies have investigated these associations in East Asian populations. The results of these studies, however, have been inconsistent. A meta-analysis was performed to assess the associations of the most published polymorphisms, including CSK rs1378942, CYP17A1 rs11191548, MTHFR rs17367504, and FGF5 rs16998073 polymorphisms with hypertension.
Published literature from PubMed and Embase databases was retrieved. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using fixed- or random-effects model.
Seven studies (16,368 cases /19,707 controls) for CSK rs1378942 polymorphism, seven studies (15,688 cases /18,784 controls) for CYP17A1 rs11191548 polymorphism, four studies (7994 cases / 12,844 controls) for MTHFR rs17367504 polymorphism, and three studies (6026 cases / 8393 controls) for FGF5 rs16998073 polymorphism were included in the meta-analysis. The results suggested that both CYP17A1 rs11191548 and FGF5 rs16998073 polymorphisms were significantly associated with hypertension risk in East Asians (CYP17A1 rs11191548 (random effect model): OR=1.16, 95% CI 1.07-1.25, p=3.59×10(-4), I(2)=78.2%, p (heterogeneity)=1.14×10(-4); FGF5 rs16998073 (random effect model): OR=1.30, 95% CI 1.23-1.37, p=6.29×10(-21), I(2)=65.0%, p (heterogeneity)=0.009); whereas no significant association was observed for CSK rs1378942 (fix effect model: OR=1.09, 95% CI 0.98-1.22, p=0.128, I(2)=0.0%, p (heterogeneity)=0.820), or MTHFR rs17367504 (fix effect model: OR=1.06, 95% CI 0.98-1.14, p=0.126, I(2)=0.0%, p (heterogeneity)=0.822).
The present meta-analysis indicated significant associations of both CYP17A1 rs11191548 and FGF5 rs16998073 polymorphisms with hypertension susceptibility in East Asians.
最近的全基因组关联研究在欧洲人身上确定了 8 个高血压易感性基因座。随后,几项研究在东亚人群中调查了这些关联。然而,这些研究的结果并不一致。进行了荟萃分析,以评估最发表的多态性与高血压的关联,包括 CSK rs1378942、CYP17A1 rs11191548、MTHFR rs17367504 和 FGF5 rs16998073 多态性。
从 PubMed 和 Embase 数据库中检索已发表的文献。使用固定或随机效应模型计算合并的比值比(OR)和 95%置信区间(CI)。
纳入了 7 项关于 CSK rs1378942 多态性的研究(16368 例/19707 例对照),7 项关于 CYP17A1 rs11191548 多态性的研究(15688 例/18784 例对照),4 项关于 MTHFR rs17367504 多态性的研究(7994 例/12844 例对照),3 项关于 FGF5 rs16998073 多态性的研究(6026 例/8393 例对照)。荟萃分析的结果表明,CYP17A1 rs11191548 和 FGF5 rs16998073 多态性均与东亚人群的高血压风险显著相关(CYP17A1 rs11191548(随机效应模型):OR=1.16,95%CI 1.07-1.25,p=3.59×10(-4),I(2)=78.2%,p(异质性)=1.14×10(-4);FGF5 rs16998073(随机效应模型):OR=1.30,95%CI 1.23-1.37,p=6.29×10(-21),I(2)=65.0%,p(异质性)=0.009);而 CSK rs1378942 (固定效应模型)没有观察到显著的关联(OR=1.09,95%CI 0.98-1.22,p=0.128,I(2)=0.0%,p(异质性)=0.820),或 MTHFR rs17367504 (固定效应模型)(OR=1.06,95%CI 0.98-1.14,p=0.126,I(2)=0.0%,p(异质性)=0.822)。
本荟萃分析表明,CYP17A1 rs11191548 和 FGF5 rs16998073 多态性与东亚人群的高血压易感性显著相关。