MTHFR A1298C gene polymorphism on stroke risk: an updated meta-analysis

Xiaobo Dong; Jun Wang; Gesheng Wang; Jiayue Wang; Lei Wang; Yong Du

doi:10.1186/s41021-021-00208-z

MTHFR A1298C gene polymorphism on stroke risk: an updated meta-analysis

Genes Environ. 2021 Sep 25;43(1):40. doi: 10.1186/s41021-021-00208-z.

Authors

Xiaobo Dong^#¹, Jun Wang^#², Gesheng Wang³, Jiayue Wang¹, Lei Wang¹, Yong Du¹

Affiliations

¹ The Third department of Encephalopathy, Dongfang Hospital Beijing University of Chinese Medicine, No. 6, Area 1, Fangxing Garden Fangzhuang, Fengtai District, Beijing, 100078, China.
² Department of Neurology, Chinese PLA General Hospital, Beijing, 100039, China.
³ The Third department of Encephalopathy, Dongfang Hospital Beijing University of Chinese Medicine, No. 6, Area 1, Fangxing Garden Fangzhuang, Fengtai District, Beijing, 100078, China. wanggesheng0623@163.com.

^# Contributed equally.

Abstract

Background: Previous studies have shown the effect of MTHFR A1298C gene polymorphism on stroke risk. But the results of published studies remained inconclusive and controversial. So we conducted a meta-analysis to accurately estimate the potential association between MTHFR A1298C gene polymorphism and stroke susceptibility.

Methods: A systematic literature search on Embase, Pubmed, Web of Science, Cochrane Library, China National Knowledge Infrastructure (CNKI) and WanFang electronic database identified 40 articles including 5725 cases and 8655 controls. Strength of association was evaluated by pooled odds ratio (OR), 95% confidence interval (CI) and p value. Funnel plots and Begger's regression test were applied for testing the publication bias. Statistical analysis of all data was performed by Stata 12.0.

Results: The meta-analysis results indicated a significant relationship between MTHFR gene A1298C polymorphisms and stoke risk under the C allelic genetic model (OR = 1.19, 95%CI = 1.07-1.32, p = 0.001), dominant genetic model (OR = 1.19, 95%CI = 1.06-1.33, p = 0.004) and recessive genetic model (OR = 1.43, 95%CI =1.15-1.77, p = 0.001). In subgroup analysis, we discovered obvious correlation in three genetic model of Asian, stroke type, adult by ethnicity, population, stroke type, source of control and case size. Additionally, in studies of control from hospital and case size equal 100, obvious correlation was also found in the three genetic model.

Conclusions: Our meta-analysis results indicated that there was evidence to support the correlation between MTHFR A1298C polymorphism and stroke susceptibility, especially in adults and ischemic stroke.

Keywords: MTHFR A1298C; Meta-analysis; Polymorphism; Stroke.