Department of Emergency, Zhongshan Hospital, Fudan University, Shanghai, China.
School of Public Health, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Arch Med Res. 2014 Jan;45(1):76-83. doi: 10.1016/j.arcmed.2013.10.002. Epub 2013 Dec 11.
Emerging evidences have shown that the Glu504Lys variant in ALDH2 gene may greatly reduce the ability of ALDH2 to metabolize acetaldehyde, which could increase the risk of coronary artery disease (CAD) and myocardial infarction (MI). However, the reported results are still conflicting. To investigate the association between ALDH2 Glu504Lys polymorphism and the risk of CAD and MI in Asians, we analyzed all available studies in a meta-analysis.
A literature search of PubMed, Embase, Web of Science and Chinese BioMedical (CBM) databases was conducted for articles published before March 1, 2013. The principal outcome measure was the crude odds ratios (ORs) with their corresponding confidence intervals (95% CIs) for evaluating the strength of the association.
Meta-analysis showed that carriers of ALDH2 504lys allele were associated with increased risks of both CAD and MI (CAD: OR = 1.28, 95% CI: 1.10-1.48, p = 0.001; MI: OR = 1.58, 95% CI: 1.15-2.19, p = 0.005). Subgroup analysis by country showed significant correlations between mutant genotypes (Glu/Lys + Lys/Lys) and increased risk to MI among Chinese and Korean populations (Chinese: OR = 1.89, 95% CI: 1.16-3.09, p = 0.011; Korean: OR = 1.69, 95%CI: 1.12-2.55, p = 0.013), whereas similar associations were not observed among Japanese populations.
The current meta-analysis provides strong evidence that ALDH2 Glu504Lys polymorphism may be associated with increased risk of CAD and MI in East Asians, especially among Chinese and Korean populations. However, more detailed and well-designed studies are still warranted to confirm these findings.
越来越多的证据表明,ALDH2 基因中的 Glu504Lys 变异可能大大降低 ALDH2 代谢乙醛的能力,从而增加患冠心病(CAD)和心肌梗死(MI)的风险。然而,目前的研究结果仍存在争议。为了探讨 ALDH2 Glu504Lys 多态性与亚洲人群 CAD 和 MI 发病风险的关系,我们采用荟萃分析的方法对所有相关研究进行了分析。
计算机检索 PubMed、Embase、Web of Science 和中国生物医学文献数据库(CBM),检索时限均为建库至 2013 年 3 月 1 日。主要结局指标为评估相关性的粗比值比(OR)及其相应的 95%可信区间(95%CI)。
荟萃分析显示,ALDH2 504lys 等位基因携带者患 CAD 和 MI 的风险均增加(CAD:OR=1.28,95%CI:1.10-1.48,p=0.001;MI:OR=1.58,95%CI:1.15-2.19,p=0.005)。按国家进行的亚组分析显示,在中国和韩国人群中,突变基因型(Glu/Lys+Lys/Lys)与 MI 发病风险增加之间存在显著相关性(中国人:OR=1.89,95%CI:1.16-3.09,p=0.011;韩国人:OR=1.69,95%CI:1.12-2.55,p=0.013),而在日本人中未观察到类似的相关性。
目前的荟萃分析提供了强有力的证据,表明 ALDH2 Glu504Lys 多态性可能与东亚人群 CAD 和 MI 的发病风险增加相关,尤其是在中国和韩国人群中。然而,仍需要更详细和精心设计的研究来证实这些发现。