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首页> 外文期刊>The journal of obstetrics and gynaecology research >Association study between CYP17 gene polymorphism and endometriosis risk: A meta-analysis
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Association study between CYP17 gene polymorphism and endometriosis risk: A meta-analysis

机译:CYP17基因多态性与子宫内膜异位症风险的关联研究:一项荟萃分析

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摘要

The cytochrome P450 subfamily 17 (CYP17) gene T>C polymorphism is associated with endometriosis risk. However, studies on the association between the genotyping of MspA1 polymorphism in the 5-untranslated region of the CYP17 gene and endometriosis risk have reported controversial results. The aim of the present study was to obtain a more precise estimate of the relationship of CYP17 gene polymorphism with endometriosis risk. Relevant articles published up to April 2014 were obtained from Pubmed, Embase, and Cochrane Central electronic databases. Case-control studies about the association between CYP17 gene polymorphisms and endometriosis were selected. Eligible data were extracted by two independent reviewers. The strength of the association between CYP17 and endometriosis was assessed by pooled odds ratios (OR) with 95% confidence intervals (CI). Eligible case-control studies involving 1000 cases and 1167 controls were analyzed from 280 studies. The pooled results showed no association between the CYP17 gene T>C polymorphism and endometriosis risk in the overall population (CC vs TT: OR=0.92, 95% CI=0.52-1.61, P=0.762; TC vs TT: OR=1.01, 95% CI=0.72-1.42, P=0.949; dominant model: OR=0.94, 95% CI=0.64-1.39, P=0.763; recessive model: OR=0.93, 95% CI=0.64-1.35, P=0.712). In the subgroup analysis based on ethnicity, no significant association was found in Asians, Caucasians and mixed population under a recessive model (Asians: OR=0.76, 95% CI=0.53-1.07, P=0.118; Caucasians: OR=2.47, 95% CI=0.45-13.66, P=0.300; mixed population: OR=1.40, 95% CI=0.65-3.02, P=0.712). In conclusion, the meta-analysis suggested that the CYP17 gene polymorphism was not associated with endometriosis risk. Considering the limited sample size and ethnicity included in our meta-analysis, an updated meta-analysis needs to be conducted when larger and more well-designed studies are published.
机译:细胞色素P450亚家族17(CYP17)基因T> C多态性与子宫内膜异位症风险相关。然而,有关CYP17基因5个非翻译区MspA1多态性的基因型分型与子宫内膜异位症风险之间关系的研究报道了有争议的结果。本研究的目的是获得CYP17基因多态性与子宫内膜异位症风险之间关系的更精确估计。从Pubmed,Embase和Cochrane Central电子数据库获得了截至2014年4月的相关文章。选择关于CYP17基因多态性与子宫内膜异位症相关性的病例对照研究。合格的数据由两名独立的审阅者提取。 CYP17与子宫内膜异位症之间的关联强度通过合并比值比(OR)和95%置信区间(CI)进行评估。从280个研究中分析了涉及1000个病例和1167个对照的合格病例对照研究。汇总结果显示CYP17基因T> C多态性与总人群子宫内膜异位症风险之间无关联(CC vs TT:OR = 0.92,95%CI = 0.52-1.61,P = 0.762; TC vs TT:OR = 1.01, 95%CI = 0.72-1.42,P = 0.949;优势模型:OR = 0.94,95%CI = 0.64-1.39,P = 0.763;隐性模型:OR = 0.93,95%CI = 0.64-1.35,P = 0.712) 。在基于种族的亚组分析中,在隐性模型下,亚洲人,高加索人和混合人口中没有发现显着关联(亚洲人:OR = 0.76,95%CI = 0.53-1.07,P = 0.118;白种人:OR = 2.47、95 %CI = 0.45-13.66,P = 0.300;混合群体:OR = 1.40,95%CI = 0.65-3.02,P = 0.712)。总之,荟萃分析提示CYP17基因多态性与子宫内膜异位症风险无关。考虑到我们的荟萃分析中所包括的样本量和种族有限,当发表更大且设计更完善的研究时,需要进行更新的荟萃分析。

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