Jiang You, Zhang Jun, Wu Yuee, Wang Jian, Li Liang
Department of General Surgery, Hefei Second People's Hospital, Anhui Medical University, Hefei, Anhui, 230011, China.
Department of Electrocardiogram Diagnosis, The Second Affiliated Hospital, Anhui Medical University, Hefei, Anhui, 230060, China.
Oncotarget. 2017 Oct 19;8(60):102401-102412. doi: 10.18632/oncotarget.22060. eCollection 2017 Nov 24.
To date, the relationship between the aldehyde dehydrogenases-2 (ALDH2) rs671 G>A (Glu504Lys) polymorphism and gastric cancer (GC) risk has not been thoroughly elucidated. To derive a more precise estimation of the effect of the ALDH2 rs671 G>A polymorphism on GC, we conducted this meta-analysis. We searched for qualified studies in the Embase, PubMed, Wang Fan and China National Knowledge Infrastructure databases. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the association. A total of 6,421 GC patients and 8,832 control subjects were included in the present study. The pooled results indicated no significant relationship between the ALDH2 rs671 G>A polymorphism and GC susceptibility in all genetic models. A stratified analysis by country showed that the ALDH2 rs671 G>A polymorphism might be a risk factor for GC in Japan (Allele model: = 0.034; Dominant model: = 0.040); however, the result was nonsignificant when the Bonferroni correction and false discovery rate (FDR) were applied. In subgroup analyses by drinking status in the dominant model, our study revealed that the ALDH2 rs671 G>A polymorphism significantly increased the risk of GC for drinkers (dominant model: < 0.001). No relationship between the ALDH2 rs671 G>A polymorphism and GC risk was observed in any other subgroup. Our present study indicated no association between the ALDH2 rs671 G>A polymorphism and GC risk in Eastern Asian populations. However, the ALDH2 rs671 G>A polymorphism can significantly increase GC risk for drinkers.
迄今为止,醛脱氢酶2(ALDH2)基因rs671 G>A(Glu504Lys)多态性与胃癌(GC)风险之间的关系尚未得到充分阐明。为了更精确地评估ALDH2 rs671 G>A多态性对胃癌的影响,我们进行了这项荟萃分析。我们在Embase、PubMed、万方和中国知网数据库中检索了合格的研究。计算合并比值比(OR)和95%置信区间(CI)以评估相关性。本研究共纳入6421例胃癌患者和8832例对照受试者。合并结果表明,在所有遗传模型中,ALDH2 rs671 G>A多态性与胃癌易感性之间均无显著关系。按国家进行的分层分析显示,ALDH2 rs671 G>A多态性可能是日本人群患胃癌的危险因素(等位基因模型: = 0.034;显性模型: = 0.040);然而,应用Bonferroni校正和错误发现率(FDR)后,结果无统计学意义。在显性模型中按饮酒状态进行的亚组分析中,我们的研究表明,ALDH2 rs671 G>A多态性显著增加了饮酒者患胃癌的风险(显性模型: < 0.001)。在任何其他亚组中均未观察到ALDH2 rs671 G>A多态性与胃癌风险之间的关系。我们目前的研究表明,在东亚人群中,ALDH2 rs671 G>A多态性与胃癌风险之间无关联。然而,ALDH2 rs671 G>A多态性可显著增加饮酒者患胃癌的风险。