Kang Shaosan, Zhao Yansheng, Wang Lei, Liu Jian, Chen Xi, Liu Xiaofeng, Shi Zhijie, Gao Weixing, Cao Fenghong
Department of Urology, North China University of Science and Technology Affiliated Hospital, Tangshan 063000, People's Republic of China,
Department of Imaging, Kailuan General Hospital, Tangshan 063000, People's Republic of China.
Cancer Manag Res. 2018 Aug 1;10:2377-2387. doi: 10.2147/CMAR.S171305. eCollection 2018.
The association between vitamin D receptor gene (rs1544410) polymorphism and prostate cancer (PCa) risk has been investigated by numerous previous studies, which yielded inconsistent results. We conducted this meta-analysis to derive a relatively precise description of this association.
All studies published up to December 2017 were identified via a systematic search of PubMed, Embase, and China National Knowledge Infrastructure databases. Pooled odds ratios (ORs) with their 95% confidence intervals (CIs) were estimated to describe the strength of the relationship between and PCa risk.
In this meta-analysis, 27 studies with 9,993 cases and 9,345 controls were included. The pooled results revealed that polymorphism was not associated with PCa risk in the overall analysis. Moreover, no significant relationship was found in the subgroup analyses by ethnicities, genotyping methods, Hardy-Weinberg equilibrium status, and Gleason score. In the stratified analysis by the source of controls and clinical stages, controls of benign prostatic hyperplasia (BPH) seemed to be in the particular groups in which the association of PCa risk with polymorphism was significant (Bb vs. bb: OR=0.643, 95% CI=0.436-0.949, =0.026; BB/Bb vs. bb: OR=0.627, 95% CI=0.411-0.954, =0.029; B vs. b: OR=0.715, 95% CI=0.530-0.965, =0.029).
Our results suggest that polymorphism is weakly associated with PCa risk, and hence, it cannot be considered as a predictor of the occurrence and development of PCa in clinical practice. Future studies with a larger number of samples are needed to verify our results.
此前已有众多研究探讨了维生素D受体基因(rs1544410)多态性与前列腺癌(PCa)风险之间的关联,但结果并不一致。我们进行了这项荟萃分析,以得出关于这种关联的相对精确的描述。
通过系统检索PubMed、Embase和中国知网数据库,确定截至2017年12月发表的所有研究。估计合并比值比(OR)及其95%置信区间(CI),以描述rs1544410与PCa风险之间关系的强度。
在这项荟萃分析中,纳入了27项研究,共9993例病例和9345例对照。汇总结果显示,在总体分析中,rs1544410多态性与PCa风险无关。此外,在按种族、基因分型方法、哈迪-温伯格平衡状态和 Gleason评分进行的亚组分析中,未发现显著关系。在按对照来源和临床分期进行的分层分析中,良性前列腺增生(BPH)对照似乎属于PCa风险与rs1544410多态性存在显著关联的特定组(Bb与bb:OR = 0.643,95%CI = 0.436 - 0.949,P = 0.026;BB/Bb与bb:OR = 0.627,95%CI = 0.411 - 0.954,P = 0.029;B与b:OR = 0.715,95%CI = 0.530 - 0.965,P = 0.029)。
我们的结果表明,rs1544410多态性与PCa风险存在弱关联,因此,在临床实践中不能将其视为PCa发生和发展的预测指标。需要更多样本量的未来研究来验证我们的结果。