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亚甲基四氢叶酸还原酶基因 C677T 多态性与多囊卵巢综合征风险的关联:系统评价和荟萃分析更新。

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

机构信息

Department of Medical Genetics, College of Basic Medical Science, Third Military Medical University, Chongqing 400038, PR China.

State Key Laboratory of Trauma, Burns and Combined Injury, Center of Bone Metabolism and Repair, Trauma Center, Institute of Surgery Research, Daping Hospital, Third Military Medical University, PR China.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2014 Jan;172:56-61. doi: 10.1016/j.ejogrb.2013.10.001. Epub 2013 Oct 10.

Abstract

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 (CT 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.

摘要

目的

通过严格审查、分析和更新现有证据,重新评估亚甲基四氢叶酸还原酶(MTHFR)基因 C677T 多态性与多囊卵巢综合征(PCOS)风险之间的关联。MTHFR C677T 多态性已被研究为心脏病、中风和高血压等多种常见疾病的可能危险因素。之前的一项荟萃分析显示,其与 PCOS 无关联,但该分析可能存在缺陷。现在已经进行了更多的研究,但结果仍不确定。

研究设计

选择包含 MTHFR C677T 基因型频率的病例对照研究,并使用比值比(OR)和 95%置信区间(CI)来评估关联的强度。统计分析使用 Review Manager(版本 5.2)和 Stata(版本 11.0)软件进行。

结果

共纳入 9 项病例对照研究,包括 638 例 PCOS 患者和 759 例健康对照。荟萃分析显示,在显性模型(TT+CT 与 CC:OR=1.65,95%CI=1.28-2.12,P<0.0001)和杂合子比较(CT 与 CC:OR=1.83,95%CI=1.17-2.87,P=0.008)中存在显著影响。按种族分层的亚组分析显示,MTHFR C677T 变异与欧洲人群的 PCOS 风险显著相关(TT+CT 与 CC:OR=2.16,95%CI=1.50-3.12,P<0.0001;CT 与 CC:OR=2.11,95%CI=1.15-3.87,P=0.02),但与亚洲人群无关(TT+CT 与 CC:OR=1.29,95%CI=0.91-1.82,P=0.15;CT 与 CC:OR=1.31,95%CI=0.91-1.90,P=0.15)。

结论

本荟萃分析表明,677T 等位基因增加了 PCOS 的易感性,这种相关性在欧洲人群中似乎比在亚洲人群中更为强烈。

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