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谷胱甘肽S-转移酶T1基因缺失/存在多态性与胃癌风险关联的Meta分析

Meta-analysis of the association of glutathione S-transferase T1 null/presence gene polymorphism with the risk of gastric carcinoma.

作者信息

Meng Yuan-Biao, Cai Xiao-Yong, Lu Wen-Qi, Yang Li-Hua, Gan Ting-Qing, Drummen Gregor P C

机构信息

Department of General Surgery, The West District of the First Affiliated Hospital of GuangXi Medical University, Nanning, 530021, China.

出版信息

Mol Biol Rep. 2014 Feb;41(2):639-49. doi: 10.1007/s11033-013-2902-y. Epub 2013 Dec 19.

Abstract

A possible association of glutathione S-transferase T1 (GSTT1) null/presence gene polymorphism and an increased risk of developing gastric carcinoma is still unclear and hotly debated. This investigation was performed to assess the association of the GSTT1 null/presence gene polymorphism with the risk of gastric carcinoma via a meta-analysis to increase sample size and statistical significance. PubMed, Cochrane Library and CBM-disc (China Biological Medicine Database) were searched on March 1, 2013, association reports were identified, and eligible studies were recruited and synthesized. Fifty-two reports were found to be suitable for this meta-analysis for the association of the GSTT1 null genotype with gastric carcinoma risk. The results showed that there was a significantly increased gastric carcinoma risk when the GSTT1 null genotype was present in the overall population (OR 1.21, 95 % CI 1.11-1.32, P < 0.0001), Caucasians (OR 1.25, 95 % CI 1.05-1.48, P = 0.01), East-Asians (OR 1.18, 95 % CI 1.06-1.31, P = 0.003), and Chinese (OR 1.24, 95 % CI 1.07-1.44, P = 0.005). However, no statistically relevant association could be established for the Indian ethnic group (OR 1.33, 95 % CI 0.94-1.90, P = 0.11). In conclusion, the GSTT1 null genotype is associated with an increased gastric carcinoma risk in the overall population, Caucasians, East-Asians, and Chinese.

摘要

谷胱甘肽S-转移酶T1(GSTT1)基因缺失/存在多态性与胃癌发生风险增加之间可能存在的关联仍不明确且备受争议。本研究旨在通过荟萃分析评估GSTT1基因缺失/存在多态性与胃癌风险的关联,以增加样本量并提高统计显著性。于2013年3月1日检索了PubMed、Cochrane图书馆和中国生物医学文献数据库(CBM-disc),识别关联报告,并纳入符合条件的研究进行综合分析。共发现52篇报告适用于本荟萃分析,以探讨GSTT1基因缺失基因型与胃癌风险的关联。结果显示,在总体人群(比值比1.21,95%可信区间1.11 - 1.32,P < 0.0001)、高加索人(比值比1.25,95%可信区间1.05 - 1.48,P = 0.01)、东亚人(比值比1.18,95%可信区间1.06 - 1.31,P = 0.003)和中国人(比值比1.24,95%可信区间1.07 - 1.44,P = 0.005)中,GSTT1基因缺失基因型与胃癌风险显著增加相关。然而,对于印度族群,未发现有统计学意义的关联(比值比1.33,95%可信区间0.94 - 1.90,P = 0.11)。总之,GSTT1基因缺失基因型与总体人群、高加索人、东亚人和中国人的胃癌风险增加相关。

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