Association between Manganese Superoxide Dismutase (MnSOD) Polymorphism and Prostate Cancer Susceptibility: A Meta-Analysis

Xiao Li, Min Shen, Hongzhou Cai, Kang Liu, Yiyang Liu, Zheng-Chun Huang, C. Liang, Xiaheng Deng, Jiaxin Ye, Qing Zou, J. Li
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引用次数: 10

Abstract

Background Previous studies have investigated the relationship between manganese superoxide dismutase (MnSOD) Val16Ala polymorphism and prostate cancer susceptibility, but the results have remained controversial. This meta-analysis was therefore performed to clarify this association. Methods The databases PubMed, Embase and Web of Science were searched for relevant available studies. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to evaluate the strength of the association. Publication bias was estimated using Begg's funnel plots and Egger's regression test. Trial sequential analysis was used to reduce the risk of type I error and estimate whether the evidence of the results was sufficient. Results Overall, a significant increased risk of prostate cancer was associated with MnSOD Val16Ala polymorphism for the heterozygote model (OR = 1.14; 95% CI, 1.05-1.24), homozygote model (OR = 1.18; 95% CI, 1.02-1.36), dominant model (OR = 1.24; 95% CI, 1.07-1.44) and recessive model (OR = 1.10; 95% CI, 0.96-1.24). In the subgroup analysis by genotyping method, the results were statistically significant for the TaqMan and PCR-RFLP methods. In addition, when stratified by sample size, statistically significant increased risks were found among both large samples and small samples. Furthermore, when stratified by source of control, significant results were detected in both population-based controls and hospital-based controls. By trial sequential analyses, these findings in the current study were shown to be based on sufficient evidence. Conclusions This meta-analysis indicated that the Ala allele of the MnSOD gene polymorphism increases prostate cancer susceptibility.
锰超氧化物歧化酶(MnSOD)多态性与前列腺癌易感性的关系:一项荟萃分析
背景以往的研究已经探讨了锰超氧化物歧化酶(MnSOD) Val16Ala多态性与前列腺癌易感性的关系,但结果仍存在争议。因此,本荟萃分析是为了澄清这种关联。方法检索PubMed、Embase和Web of Science数据库中相关文献。计算合并优势比(ORs)和95%置信区间(CIs)来评估相关性的强度。发表偏倚采用Begg’s漏斗图和Egger’s回归检验。试验序贯分析用于降低I型错误的风险,并评估结果的证据是否充分。结果总体而言,在杂合子模型中,前列腺癌风险显著增加与MnSOD Val16Ala多态性相关(OR = 1.14;95% CI, 1.05-1.24),纯合子模型(OR = 1.18;95% CI, 1.02-1.36),优势模型(OR = 1.24;95% CI, 1.07-1.44)和隐性模型(OR = 1.10;95% ci, 0.96-1.24)。在基因分型亚组分析中,TaqMan法和PCR-RFLP法的结果均有统计学意义。此外,当按样本量分层时,在大样本和小样本中都发现了统计学上显著增加的风险。此外,当按对照来源分层时,在基于人群的对照和基于医院的对照中都发现了显著的结果。通过试验序列分析,本研究的这些发现是建立在充分证据的基础上的。结论MnSOD基因多态性的Ala等位基因增加了前列腺癌的易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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