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GSTM1 无基因型导致男性不育风险增加:荟萃分析。

GSTM1 null genotype contributes to increased risk of male infertility: a meta-analysis.

机构信息

Reproductive Medicine Center, Department of Obstetrics and Gynecology, Meizhou People's hospital, Meizhou, 514031, China.

出版信息

J Assist Reprod Genet. 2012 Aug;29(8):837-45. doi: 10.1007/s10815-012-9790-2. Epub 2012 May 24.

Abstract

BACKGROUND

Many studies have investigated the association between Glutathione S-Transferase M 1 (GSTM1) null genotype and risk of male infertility, but the impact of GSTM1 null genotype on infertility risk is unclear owing to the obvious inconsistency among those studies. This study aimed to quantify the strength of association between GSTM1 null genotype and risk of male infertility.

METHODS

We searched the PubMed, Embase and Wangfang databases for studies investigating the association between GSTM1 null genotype and risk of male infertility. We estimated pooled odds ratio (OR) with its 95 % confidence interval (95 % CI) to assess this possible association.

RESULTS

Twelve case-control studies with 1, 589 infertility cases and 1, 537 controls were included. Meta-analysis of total 12 studies showed that GSTM1 null genotype was associated with increased risk of male infertility (OR = 1.34, 95%CI 1.02-1.77, P = 0.036). In subgroup analysis of Caucasians, there was also an obvious association between GSTM1 null genotype and increased risk of male infertility (OR = 1.51, 95%CI 1.11-2.05, P = 0.006). Sensitivity analyses by sequential omission of individual studies or omitting studies without high quality did not significantly alter the overall pooled OR. Cumulative meta-analysis further showed a trend of more obvious association as information accumulated. No evidence of publication bias was observed.

CONCLUSION

Meta-analyses of available data suggest that GSTM1 null genotype contributes to increased risk of male infertility.

摘要

背景

许多研究已经探讨了谷胱甘肽 S-转移酶 M1(GSTM1)缺失基因型与男性不育风险之间的关联,但由于这些研究之间存在明显的不一致性,GSTM1 缺失基因型对不育风险的影响尚不清楚。本研究旨在量化 GSTM1 缺失基因型与男性不育风险之间的关联强度。

方法

我们检索了 PubMed、Embase 和万方数据库中关于 GSTM1 缺失基因型与男性不育风险之间关联的研究。我们用合并的比值比(OR)及其 95%置信区间(95%CI)来评估这种可能的关联。

结果

纳入了 12 项病例对照研究,共包括 1589 例不育病例和 1537 例对照。对总共 12 项研究的荟萃分析表明,GSTM1 缺失基因型与男性不育风险增加相关(OR=1.34,95%CI 1.02-1.77,P=0.036)。在白种人亚组分析中,GSTM1 缺失基因型与男性不育风险增加也存在明显关联(OR=1.51,95%CI 1.11-2.05,P=0.006)。通过逐个排除个体研究或排除没有高质量的研究进行敏感性分析,并未显著改变整体合并 OR。累积荟萃分析进一步表明,随着信息的积累,关联更加明显。未发现发表偏倚的证据。

结论

对现有数据的荟萃分析表明,GSTM1 缺失基因型增加了男性不育的风险。

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