Wang Yinglei, Zhang YingYing, Meng Haihong, Hou Xianghua, Li Zhonghai, Liu Qingpeng, Meng Lin
Urology Department, Jining Medical College Affiliated Hospital, Shandong, 272029, China,
Cell Biochem Biophys. 2015 Mar;71(2):983-91. doi: 10.1007/s12013-014-0297-6.
Published data on the association between CYP17 rs743572 polymorphism and risk of PC showed inconclusive results. The aim of this study was to further estimate the pooled effect size of rs743572 polymorphism and PC progression via large-scale meta-analysis. We searched the case-control studies of rs743572 polymorphism and PC risk in PubMed, Embase, and Web of Science databases up to February 2014. Odds ratios (ORs) along with 95 % confidence intervals (CIs) were pooled by means of both fixed effects model and random effects model. A total of 38 publications consisting of 42 studies with 15,735 cases and 17,825 controls were included in this meta-analysis. Overall, no significant association was found between rs743572 polymorphism and PC risk. Stratified analyses by control source and sample size did not provide significant results. However, there was a borderline association in African population under A2A2 versus A1A2 + A1A1 genetic model (OR = 1.39, 95 % CI: 1.01-1.92, P = 0.975, I (2) = 0.0 %). Results from the current meta-analysis suggested that CYP17 rs743572 polymorphism might modify the risk of PC in the subjects of African decent.
已发表的关于CYP17基因rs743572多态性与前列腺癌风险之间关联的数据结果并不确定。本研究的目的是通过大规模荟萃分析进一步评估rs743572多态性与前列腺癌进展的合并效应量。我们检索了截至2014年2月在PubMed、Embase和科学网数据库中有关rs743572多态性与前列腺癌风险的病例对照研究。采用固定效应模型和随机效应模型汇总比值比(OR)及其95%置信区间(CI)。本荟萃分析共纳入38篇文献,包括42项研究,涉及15735例病例和17825例对照。总体而言,未发现rs743572多态性与前列腺癌风险之间存在显著关联。按对照来源和样本量进行的分层分析未得出显著结果。然而,在非洲人群中,在A2A2与A1A2 + A1A1遗传模型下存在临界关联(OR = 1.39,95% CI:1.01 - 1.92,P = 0.975,I² = 0.0%)。当前荟萃分析的结果表明,CYP17基因rs743572多态性可能会改变非洲裔人群患前列腺癌的风险。