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锰超氧化物歧化酶基因多态性与前列腺癌风险的关联:一项荟萃分析。

Association between manganese superoxide dismutase gene polymorphism and risk of prostate cancer: a meta-analysis.

作者信息

Liwei Liu, Chunyu Liu, Ruifa Han

机构信息

Tianjin Institution of Urology, The 2nd. Hospital of Tianjin Medical University, Tianjin, China.

出版信息

Urology. 2009 Oct;74(4):884-8. doi: 10.1016/j.urology.2008.11.016. Epub 2009 Jul 31.

Abstract

OBJECTIVES

To examine the association between 2 mitochondrial manganese superoxide dismutase (MnSOD) genetic polymorphisms (Ala-9Val and Ala-16Val) and prostate cancer susceptibility.

METHODS

A comprehensive search was conducted to identify all case-control studies of MnSOD polymorphisms and prostate cancer risk. Statistical analysis was performed with the software program Stata, version 8.0, and Review Manage, version 4.2.

RESULTS

A total of 9 eligible studies, including 3268 cases and 5907 controls, relating the MnSOD polymorphism to the risk of prostate cancer were identified. For the Ala-9Val polymorphism, 5 studies, including 889 cases and 1841 controls, found no significant associations between MnSOD polymorphism and the risk of developing prostate cancer in the recessive, dominant, and co-dominant models. In the sensitivity analysis, exclusion of the study with the controls not in Hardy-Weinberg equilibrium, no significant associations were also found in the recessive (odds ratio [OR] 1.29, 95% confidence interval [CI] 0.66-2.50), dominant (OR 1.35, 95% CI 0.84-2.17), and co-dominant (OR 1.33, 95% CI 0.87-2.01) models. For the Ala-16Val polymorphism, 4 studies, including 2379 cases and 4066 controls, found no significant association between MnSOD polymorphism and the risk of developing prostate cancer in both co-dominant (OR 1.08, 95% CI 1.00-1.16), recessive (OR 1.06, 95% CI 0.94-1.20) and dominant (OR 1.14, 95% CI 1.00-1.28) models.

CONCLUSIONS

No significant association was found between the Ala-9Val and Ala-16Val polymorphisms in MnSOD and prostate cancer susceptibility.

摘要

目的

研究线粒体锰超氧化物歧化酶(MnSOD)的两种基因多态性(丙氨酸-9缬氨酸和丙氨酸-16缬氨酸)与前列腺癌易感性之间的关联。

方法

进行全面检索以确定所有关于MnSOD基因多态性与前列腺癌风险的病例对照研究。使用Stata 8.0软件程序和Review Manage 4.2软件进行统计分析。

结果

共确定了9项符合条件的研究,包括3268例病例和5907例对照,涉及MnSOD基因多态性与前列腺癌风险的关系。对于丙氨酸-9缬氨酸多态性,5项研究(包括889例病例和1841例对照)发现在隐性、显性和共显性模型中,MnSOD基因多态性与患前列腺癌的风险之间无显著关联。在敏感性分析中,排除对照组不符合哈迪-温伯格平衡的研究后,在隐性模型(比值比[OR]1.29,95%置信区间[CI]0.66 - 2.50)、显性模型(OR 1.35,95% CI 0.84 - 2.17)和共显性模型(OR 1.33,95% CI 0.87 - 2.01)中也未发现显著关联。对于丙氨酸-16缬氨酸多态性,4项研究(包括2379例病例和4066例对照)发现在共显性模型(OR 1.08,95% CI 1.00 - 1.16)、隐性模型(OR 1.06,95% CI 0.94 - 1.20)和显性模型(OR 1.14,95% CI 1.00 - 1.28)中,MnSOD基因多态性与患前列腺癌的风险之间均无显著关联。

结论

未发现MnSOD基因的丙氨酸-9缬氨酸和丙氨酸-16缬氨酸多态性与前列腺癌易感性之间存在显著关联。

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