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荟萃分析:谷胱甘肽S-转移酶T1无效等位基因与胃癌风险相关。

Meta-analysis: glutathione S-transferase T1 null allele is associated with gastric cancer risk.

作者信息

Sun Wei, Yao Li, Jiang Benchun

机构信息

Department of General Surgery, Affiliated Shengjing Hospital, China Medical University, Shenyang, 110004, Liaoning Province, China,

出版信息

Tumour Biol. 2014 Jan;35(1):239-45. doi: 10.1007/s13277-013-1029-z. Epub 2013 Aug 23.

Abstract

Allelic variant within genes encoding glutathione S-transferase T1 (GSTT1) has been suggested to be a possible risk factor of gastric cancer, but previous studies provide controversial results. This study aimed to assess the effects of GSTT1 polymorphism on gastric cancer by means of meta-analysis. We included published studies on the relationship between GSTT1 null allele and gastric cancer risk after searching electronic databases. A meta-analysis was conducted by calculating the pooled odds ratios (OR) and the 95% confidence intervals (95% CI). Forty-two studies with a total of 8,203 gastric cancer cases and 13,866 controls were included into this meta-analysis. When all 42 studies were pooled into this meta-analysis, there was a significant association between the GSTT1 null allele and gastric cancer risk (OR = 1.24, 95% CI 1.14-1.36, P < 0.00001). Sensitivity analysis by excluding individual studies showed that there was no effect on the pooled OR with 95% CI. After excluding studies with low quality, there was still a significant association between the GSTT1 null allele and gastric cancer risk (OR = 1.24, 95% CI 1.13-1.36, P < 0.00001). In the subgroup analysis, there was a significant association between the GSTT1 null allele and gastric cancer risk in both Europeans and Asians. There was no risk of publication bias in this meta-analysis. Our results suggest that GSTT1 null allele is associated with increased risk of gastric cancer.

摘要

编码谷胱甘肽S-转移酶T1(GSTT1)的基因中的等位基因变异被认为可能是胃癌的一个风险因素,但先前的研究结果存在争议。本研究旨在通过荟萃分析评估GSTT1基因多态性对胃癌的影响。我们在检索电子数据库后纳入了已发表的关于GSTT1无效等位基因与胃癌风险关系的研究。通过计算合并比值比(OR)和95%置信区间(95%CI)进行荟萃分析。本荟萃分析纳入了42项研究,共8203例胃癌病例和13866例对照。当将所有42项研究纳入该荟萃分析时,GSTT1无效等位基因与胃癌风险之间存在显著关联(OR = 1.24,95%CI 1.14 - 1.36,P < 0.00001)。通过排除个别研究进行的敏感性分析表明,对合并的OR及95%CI没有影响。排除质量较低的研究后,GSTT1无效等位基因与胃癌风险之间仍存在显著关联(OR = 1.24,95%CI 1.13 - 1.36,P < 0.00001)。在亚组分析中,欧洲人和亚洲人中GSTT1无效等位基因与胃癌风险之间均存在显著关联。该荟萃分析不存在发表偏倚风险。我们的结果表明,GSTT1无效等位基因与胃癌风险增加有关。

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