Department of Digestive internal medicine, Heping Hospital Affiliated to Changzhi Medical College, Shanxi, Changzhi 046000, China.
Department of Epidemiology, School of Public Health, Southern Medical University, Guang-dong, Guangzhou 510515, China.
Biosci Rep. 2023 Apr 26;43(4). doi: 10.1042/BSR20222553.
Widely regarded as one of the most prevalent malignancies worldwide, gastric cancer (GC) is a common clinical condition of the digestive system. Reviewing 14 meta-analyses that evaluated the association between methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and GC risk, we observed inconsistent results, and the credibility of the significant correlation between the statistical results was ignored. With the aim of further exploring the association between MTHFR C677T and A1298C and the risk of GC, we searched electronic databases, pooling 43 relevant studies and calculating odds ratios (ORs) and corresponding 95% confidence intervals (CIs) for each of the five genetic models. Subgroup and regression analyses were performed to look for sources of heterogeneity and publication bias was assessed by funnel plots. To assess the plausibility of statistically significant associations, we used the FPRP test and the Venice criteria. Overall data analysis showed that MTHFR C677T polymorphism was significantly associated with GC risk, especially in Asians, while MTHFR A1298C polymorphism was not associated with GC risk. However, in subgroup analysis by hospital-based controls, we found that MTHFR A1298C might be a protective factor for GC. After credibility assessment, the statistical association between MTHFR C677T and GC susceptibility study was classified as 'less credible positive result', while the result of MTHFR A1298C was considered unreliable. In summary, the present study strongly suggests that MTHFR C677T and A1298C polymorphisms are not significantly associated with the GC risk.
胃癌(GC)被广泛认为是全球最普遍的恶性肿瘤之一,是一种常见的消化系统疾病。我们回顾了 14 项评估亚甲基四氢叶酸还原酶(MTHFR)基因多态性与 GC 风险之间关系的荟萃分析,观察到结果不一致,并且忽略了统计结果之间显著相关性的可信度。为了进一步探讨 MTHFR C677T 和 A1298C 与 GC 风险之间的关系,我们搜索了电子数据库,汇集了 43 项相关研究,并计算了每种 5 种遗传模型的优势比(OR)和相应的 95%置信区间(CI)。进行亚组和回归分析以寻找异质性的来源,并通过漏斗图评估发表偏倚。为了评估统计学显著关联的合理性,我们使用了 FPRP 检验和威尼斯标准。总体数据分析表明,MTHFR C677T 多态性与 GC 风险显著相关,尤其是在亚洲人群中,而 MTHFR A1298C 多态性与 GC 风险无关。但是,在基于医院对照的亚组分析中,我们发现 MTHFR A1298C 可能是 GC 的保护因素。经过可信度评估,MTHFR C677T 与 GC 易感性研究之间的统计关联被归类为“可信度较低的阳性结果”,而 MTHFR A1298C 的结果则被认为不可靠。总之,本研究强烈表明 MTHFR C677T 和 A1298C 多态性与 GC 风险无显著相关性。