XRCC7基因多态性与胶质瘤风险:一项前瞻性病例对照研究

IF 0.3 Q4 SURGERY
Deepak Choudhary, B. Mahajan, M. Sumi, Binita Dholakia, Sumit Bhandari, Niraj R. Ghimire, S. Saluja, Shaam Bodeliwala, W. Wani, A. Jagetia
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引用次数: 1

摘要

【摘要】目的探讨XRCC7基因多态性与胶质瘤的关系。材料与方法采用病例对照研究,分析30例组织学证实的胶质瘤患者和30例年龄和性别匹配的对照组中各种XRCC7基因型的患病率。结果胶质瘤患者中XRCC7基因GT和TT基因型的患病率明显高于对照组。在中年和男性两个亚组中患病率显著。XRCC7 GT或TT基因型的存在显著增加了发生胶质瘤的风险(优势比:13.021,2.114-80.213)。结论XRCC7多态性中T等位基因的存在可能增加胶质瘤的易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymorphism of XRCC7 Gene and Risk of Glioma: A Prospective Case–Control Study
Abstract Objective  The aim of this study is to determine association between polymorphism of XRCC7 gene and glioma. Materials and Methods  A case–control study was designed to analyze the prevalence of the various XRCC7 genotypes in 30 cases of histologically proven glioma and 30 age- and sex matched controls. Result  There is significantly higher prevalence of the GT and the TT genotypes of XRCC7 gene in cases of glioma as compared with control. The prevalence was significantly pronounced in two subgroups–middle aged and male gender. The presence of the XRCC7 GT or TT genotype conferred a significantly higher risk of developing glioma (odds ratio: 13.021,2.114–80.213). Conclusion  The presence of the T allele in XRCC7 polymorphism may increase the susceptibility to glioma.
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CiteScore
0.40
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发文量
52
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12 weeks
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