Department of Cardiac Surgery, The PLA General Hospital, Medical School of Chinese PLA, 28 Fuxing Road, Beijing, 100098, China.
Mol Biol Rep. 2013 Jul;40(7):4439-45. doi: 10.1007/s11033-013-2534-2. Epub 2013 May 13.
Angiotensinogen, one of the most important proteins in the renin-angiotensin system, plays a key role in the progress of coronary heart disease and myocardial infarction (MI). Many studies have investigated the association between angiotensinogen gene M235T polymorphism and MI risk, but the results were inconsistent. We performed a meta-analysis of 22 studies on M235T polymorphism and MI risk published before November 2012. This meta-analysis included a total of 4,606 MI cases and 4,918 controls. Overall, the per-allele odds ratio (OR) of the 235T variant for total MI risk was 1.04 (95 % CI 0.92-1.17). When a recessive model was evaluated, the OR was 1.06 (95 % CI 0.96-1.17) and under a dominant model, the OR was 0.96 (95 % CI 0.82-1.11). Under pairwise comparisons, non-significant associations were found between M235T polymorphism and MI risk (MT vs. MM, OR, 0.96, 95 % CI 0.87-1.06; TT vs. MM, OR, 1.03, 95 % CI 0.83-1.28). Subgroup analyses in the different ethnic groups and different control sources were performed and no significant association was found also. Based on the available evidence, no association between M235T polymorphism and MI risk was observed, even in the sub-analysis concerning different races and control sources. The direction of further research should focus not only on the simple relationship of M235T polymorphism and MI risk, but also on gene-gene and gene-environment interaction.
血管紧张素原是肾素-血管紧张素系统中最重要的蛋白之一,在冠心病和心肌梗死(MI)的进展中起着关键作用。许多研究已经探讨了血管紧张素原基因 M235T 多态性与 MI 风险之间的关系,但结果并不一致。我们对截至 2012 年 11 月前发表的 22 项关于 M235T 多态性与 MI 风险的研究进行了荟萃分析。该荟萃分析共纳入了 4606 例 MI 病例和 4918 例对照。总体而言,235T 变体的等位基因比值比(OR)为 1.04(95%置信区间 0.92-1.17)。当评估隐性模型时,OR 为 1.06(95%置信区间 0.96-1.17),而显性模型下的 OR 为 0.96(95%置信区间 0.82-1.11)。在两两比较中,M235T 多态性与 MI 风险之间没有发现显著关联(MT 与 MM,OR 为 0.96,95%置信区间 0.87-1.06;TT 与 MM,OR 为 1.03,95%置信区间 0.83-1.28)。在不同种族和不同对照来源的亚组分析中也未发现显著关联。基于现有的证据,未观察到 M235T 多态性与 MI 风险之间存在关联,即使在考虑不同种族和对照来源的亚分析中也是如此。进一步研究的方向不仅应关注 M235T 多态性与 MI 风险的简单关系,还应关注基因-基因和基因-环境的相互作用。