Department of Geriatrics, Qilu Hospital of Shandong University, Jinan, People's Republic of China.
Gene. 2013 Oct 15;529(1):73-9. doi: 10.1016/j.gene.2013.07.095. Epub 2013 Aug 8.
The angiotensinogen (AGT) gene M235T polymorphism has been reported to be associated with myocardial infarction (MI) and brain infarction (BI), but the results remain inconclusive. This meta-analysis was designed to clarify these controversies. Electronic databases were systematically searched before February 2013. A total of 38 studies with 17304 subjects met our inclusion criteria. In East Asian group, significant association was found between AGT M235T polymorphism and risk of MI (for dominant model: OR=1.79; 95% CI=1.04-3.06; for recessive model OR=2.01; 95% CI=1.21-3.36; for additive model OR=1.79; 95% CI=1.14-2.86) as well as BI (for dominant model: OR=1.66; 95% CI=1.22-2.27; for recessive model OR=1.78, 95% CI=1.29-2.46; for additive model: OR=1.64, 95% CI=1.34-2.00), while the M235T polymorphism did not impact the risk of MI in total population and other ethnicity. In the subgroup analyses by gender and age, there was lack of evidence for the association. This meta-analysis suggested an association between the M235T polymorphism and MI as well as BI in East Asian population. Further studies with larger numbers of worldwide participants are needed to understand the genetic basis of MI and BI.
血管紧张素原(AGT)基因 M235T 多态性与心肌梗死(MI)和脑梗死(BI)有关,但结果仍不确定。本荟萃分析旨在阐明这些争议。在 2013 年 2 月之前系统地检索了电子数据库。共有 38 项研究,共纳入 17304 例患者符合我们的纳入标准。在东亚人群中,AGT M235T 多态性与 MI 风险(对于显性模型:OR=1.79;95%CI=1.04-3.06;对于隐性模型:OR=2.01;95%CI=1.21-3.36;对于加性模型:OR=1.79;95%CI=1.14-2.86)和 BI(对于显性模型:OR=1.66;95%CI=1.22-2.27;对于隐性模型:OR=1.78,95%CI=1.29-2.46;对于加性模型:OR=1.64,95%CI=1.34-2.00)显著相关,但在总体人群和其他种族中,M235T 多态性并不影响 MI 的风险。在按性别和年龄进行的亚组分析中,缺乏相关性的证据。本荟萃分析表明,AGT M235T 多态性与东亚人群的 MI 和 BI 相关。需要进一步进行全球范围内有更多参与者的研究,以了解 MI 和 BI 的遗传基础。