Yang B, Fan S, Zhi X, Xia R, Wang Y, Zheng Q, Sun G
Guangzhou Key Laboratory of Environmental Pollution and Health Risk Assessment, Department of Preventive Medicine, School of Public Health, Sun Yat-Sen University, Guangzhou, China.
Environment and Non-Communicable Disease Research Center, School of Public Health, China Medical University, Shenyang, China.
Clin Genet. 2017 Sep;92(3):243-258. doi: 10.1111/cge.12929. Epub 2017 Mar 15.
Numerous studies have investigated the distribution of methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and their associations with diseases in China. In this study we conducted a systematic review and meta-analysis of these studies (715 eligible studies in total).Results revealed that the frequencies of the MTHFR C677T and A1298C polymorphisms varied markedly in different areas and ethnicities, and even showed geographical gradients. The MTHFR C677T polymorphism was significantly associated with 42 clinical disorders (p < 0.05), mostly relating to the diseases of circulatory system, birth defects and cancers. The association of the A1298C polymorphism with three diseases (coronary heart disease, breast cancer and neural tube defects fathers) was statistically significant (p < 0.05). However, according to the Venice criteria, only the associations of the C677T polymorphism with breast and ovarian cancers were assessed as having strong epidemiological credibility. This is the first study to provide a comprehensive assessment of the current status and gaps in genetic epidemiological study of the two polymorphisms in China, and its findings may be useful for medical and public health practices. Future studies are warranted to focus on the interactions of MTHFR genes with environmental exposure and with other genes, and to improve their methodological quality and reporting of findings.
众多研究对中国亚甲基四氢叶酸还原酶(MTHFR)C677T和A1298C基因多态性的分布及其与疾病的关联进行了调查。在本研究中,我们对这些研究(总共715项符合条件的研究)进行了系统评价和荟萃分析。结果显示,MTHFR C677T和A1298C基因多态性的频率在不同地区和种族中存在显著差异,甚至呈现出地理梯度。MTHFR C677T基因多态性与42种临床疾病显著相关(p<0.05),主要涉及循环系统疾病、出生缺陷和癌症。A1298C基因多态性与三种疾病(冠心病、乳腺癌和神经管缺陷父亲)的关联具有统计学意义(p<0.05)。然而,根据威尼斯标准,只有C677T基因多态性与乳腺癌和卵巢癌的关联被评估为具有较强的流行病学可信度。这是第一项对中国这两种基因多态性的遗传流行病学研究现状和差距进行全面评估的研究,其结果可能对医学和公共卫生实践有用。未来的研究有必要关注MTHFR基因与环境暴露以及与其他基因的相互作用,并提高其方法学质量和研究结果的报告水平。