Suppr超能文献

MTHFR基因C677T多态性与自闭症谱系障碍易感性的关联:中国汉族人群的荟萃分析

Association Between MTHFR C677T Polymorphism and Susceptibility to Autism Spectrum Disorders: A Meta-Analysis in Chinese Han Population.

作者信息

Li Chen-Xi, Liu Yi-Guang, Che Yue-Ping, Ou Jian-Lin, Ruan Wen-Cong, Yu Yong-Lin, Li Hai-Feng

机构信息

Department of Rehabilitation, the Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, China.

Department of Linguistics, Zhejiang University, Hangzhou, China.

出版信息

Front Pediatr. 2021 Mar 10;9:598805. doi: 10.3389/fped.2021.598805. eCollection 2021.

Abstract

Prior studies have examined the influence of MTHFR C677T on autism susceptibility, however, there are no consensus conclusions and specific analyses of a Chinese population. This meta-analysis included a false-positive report probability (FPRP) test to comprehensively evaluate the association of MTHFR C677T polymorphism with autism susceptibility among a Chinese Han population. A large-scale literature retrieval was conducted using various databases including PubMed, Embase, Wan Fang, and the Chinese National Knowledge Infrastructure (CNKI) up to July 31, 2020, with a total of 2,258 cases and 2,073 controls included. The strength of correlation was assessed by odds ratios (ORs) and 95% confidence intervals (95% CIs). MTHFR C677T showed a significant correlation with increased ASD susceptibility under all genetic models (T vs. C, OR = 1.89, 95% CI 1.28 to 2.79; TT vs. CC: OR = 2.44, 95% CI 1.43 to 4.15; CT vs. CC, OR = 1.73; 95% CI 1.19 to 2.51; CT + TT vs. CC: OR = 2.03, 95% CI 1.31 to 3.15; TT vs. CT + CC, OR = 1.95, 95% CI 1.21 to 3.13). Stratification analysis by region also revealed a consistent association in the Northern Han subgroup, but not in the Southern Han subgroup. Pooled minor allele frequency (MAF) of 30 studies were 45% in Northern Han and 39% in Southern Han. To avoid a possible "false positive report," we further investigated the significant associations observed in the present meta-analysis using the FPRP test, which consolidated the results. In conclusion, MTHFR C677T polymorphism is associated with the increased risk of autism in China, especially in Northern Han. For those mothers and children who are generally susceptible to autism, prenatal folate and vitamin B12 may reduce the risk that children suffer from autism, especially in Northern Han populations. In the future, more well-designed studies with a larger sample size are expected.

摘要

先前的研究已经探讨了亚甲基四氢叶酸还原酶(MTHFR)C677T对自闭症易感性的影响,然而,目前尚无共识性结论,且缺乏针对中国人群的具体分析。本荟萃分析纳入了假阳性报告概率(FPRP)检验,以全面评估MTHFR C677T基因多态性与中国汉族人群自闭症易感性之间的关联。通过使用包括PubMed、Embase、万方和中国知网(CNKI)在内的多个数据库进行大规模文献检索,检索截至2020年7月31日的文献,共纳入2258例病例和2073例对照。相关性强度通过比值比(OR)和95%置信区间(95%CI)进行评估。在所有遗传模型下,MTHFR C677T与自闭症易感性增加均呈现显著相关性(T vs. C,OR = 1.89,95%CI为1.28至2.79;TT vs. CC:OR = 2.44,95%CI为1.43至4.15;CT vs. CC,OR = 1.73;95%CI为1.19至2.51;CT + TT vs. CC:OR = 2.03,95%CI为1.31至3.15;TT vs. CT + CC,OR = 1.95,95%CI为1.21至3.13)。按地区进行的分层分析还显示,在北方汉族亚组中存在一致的关联,但在南方汉族亚组中未发现。30项研究的合并次要等位基因频率(MAF)在北方汉族中为45%,在南方汉族中为39%。为避免可能的“假阳性报告”,我们使用FPRP检验进一步研究了本荟萃分析中观察到的显著关联,结果得到了巩固。总之,MTHFR C677T基因多态性与中国自闭症风险增加相关,尤其是在北方汉族人群中。对于那些通常易患自闭症的母亲和儿童,产前补充叶酸和维生素B12可能会降低儿童患自闭症的风险,尤其是在北方汉族人群中。未来,预计会有更多设计良好、样本量更大的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8072/7987783/a1fffce8894a/fped-09-598805-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验