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首页> 外文期刊>The International journal of biological markers >Association between Manganese Superoxide Dismutase (MnSOD) Polymorphism and Prostate Cancer Susceptibility: A Meta-Analysis
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Association between Manganese Superoxide Dismutase (MnSOD) Polymorphism and Prostate Cancer Susceptibility: A Meta-Analysis

机译:锰超氧化物歧化酶(MnSOD)多态性与前列腺癌易感性之间的关联:荟萃分析。

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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. 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. 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. This meta-analysis indicated that the Ala allele of the MnSOD gene polymorphism increases prostate cancer susceptibility.
机译:先前的研究已经调查了锰超氧化物歧化酶(MnSOD)Val16Ala多态性与前列腺癌易感性之间的关系,但结果仍存在争议。因此进行了这项荟萃分析以阐明这种关联。在PubMed,Embase和Web of Science数据库中搜索了相关的可用研究。计算具有95%置信区间(CI)的合并比值比(OR),以评估关联的强度。使用Begg的漏斗图和Egger回归测试估计出版偏倚。试验顺序分析用于降低I型错误的风险,并估计结果的证据是否足够。总体而言,杂合子模型(OR = 1.14; 95%CI,1.05-1.24),纯合子模型(OR = 1.18; 95%CI,1.02-1.36),占优势的MnSOD Val16Ala多态性与前列腺癌的显着增加风险相关。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)。在通过基因分型方法进行的亚组分析中,对于TaqMan方法和PCR-RFLP方法,结果具有统计学意义。此外,当按样本量分层时,在大样本和小样本中都发现统计学上显着增加的风险。此外,按控制源分层时,在基于人群的控制和医院控制中均检测到显着结果。通过试验性顺序分析,当前研究中的这些发现被证明是基于充分的证据。这项荟萃分析表明MnSOD基因多态性的Ala等位基因会增加前列腺癌的易感性。

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