Association of methylenetetrahydrofolate reductase gene C677T polymorphism with polycystic ovary syndrome risk: a systematic review and meta-analysis update

被引:11
作者
Fu, Li-yuan [1 ]
Dai, Li-meng [1 ]
Li, Xiao-gang [2 ]
Zhang, Kun [1 ]
Bai, Yun [1 ]
机构
[1] Third Mil Med Univ, Coll Basic Med Sci, Dept Med Genet, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Doping Hosp, Ctr Trauma, Inst Surg Res,Ctr Bone Metab & Repair,State Key L, Chongqing, Peoples R China
关键词
Methylenetetrahydrofolate reductase; Polycystic ovary syndrome; Polymorphism; Meta-analysis; PLASMINOGEN-ACTIVATOR INHIBITOR-1; CARDIOVASCULAR-DISEASE; PLASMA HOMOCYSTEINE; ROTTERDAM CRITERIA; WOMEN; MTHFR; PREVALENCE; PREMATURE; DIAGNOSIS; MUTATION;
D O I
10.1016/j.ejogrb.2013.10.001
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: To re-estimate the association between methylenetetrahydrofolate reductase gene (MTHFR) C677T polymorphism and polycystic ovary syndrome (PCOS) risk by critically reviewing, analyzing and updating the current evidence. MTHFR C677T polymorphism has been studied as a possible risk factor for a variety of common conditions including heart disease, stroke and hypertension. Its association with PCOS was negative in a previous meta-analysis which had possible shortcomings. More studies have now been done but their results remain inconclusive. Study design: Available case-control studies containing genotype frequencies of MTHFR C677T were chosen, and odds ratio (OR) with 95% confidence interval (CI) was used to assess the strength of the association. Statistical analyses were performed using software Review Manager (Version 5. 2) and Stata (Version 11.0). Results: Nine case-control studies including 638 PCOS and 759 healthy controls were identified. Meta-analysis showed a significant effect in the dominant model (TT+CT vs. CC: OR = 1.65, 95%CI = 1.28-2.12, P < 0.0001) and heterozygote comparison (CF vs. CC: OR = 1.83, 95%CI = 1.17-2.87, P = 0.008). In subgroup analysis stratified by ethnicity, MTHFR C677T variant was statistically significantly relevant to PCOS risk in European populations (TT+CT vs. CC: OR = 2.16, 95%CI = 1.50-3.12, P < 0.0001; CT vs. CC: OR = 2.11, 95%CI = 1.15-3.87, P = 0.02) but not in Asian populations (TT+CT vs. CC: OR = 1.29, 95%CI = 0.91-1.82, P = 0.15; CT vs. CC: OR = 1.31, 95%CI = 0.91-1.90, P = 0.15). Conclusions: This meta-analysis indicates that the 677T allele increases PCOS susceptibility, and this relevance seems to be more intense in Europeans than in Asians. (C) 2013 Published by Elsevier Ireland Ltd.
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收藏
页码:56 / 61
页数:6
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