Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, 81 Meishan Road, Hefei, Anhui 230032, China.
Med Oncol. 2011 Mar;28(1):133-6. doi: 10.1007/s12032-010-9417-3. Epub 2010 Jan 20.
Relationship of gastric cancer with the presence of IL-10-592 polymorphism was reported with inconsistent results. The objective of this study was to quantitatively evaluate the association between IL-10-592 allele polymorphism and gastric cancer susceptibility. We performed an extensive search of relevant studies and made a meta-analysis, including 12 studies with 2,285 gastric cancer cases and 4,236 controls. The combined results based on all studies showed that there were no significant differences in genotype distribution between gastric cancer cases and controls, CC versus CA/AA (OR = 1.05, 95% CI: 0.92-1.18), CC/CA versus AA (OR = 1.16, 95% CI: 0.92-1.46), CC versus CA (OR = 1.03, 95% CI: 0.90-1.17), CC versus AA (OR = 1.10, 95% CI: 0.90-1.34), and CA versus AA (OR = 1.16, 95% CI: 0.92-1.45). When stratifying for the race, it was found that gastric cancer cases had a significantly higher frequency of CC/CA versus AA (OR = 1.31, 95% CI: (1.08-1.59) and a significantly upper frequency of CA versus AA (OR = 1.33, 95% CI: 1.09-1.63) than control in Asians. When stratifying for the location and the Lauren's classification of gastric cancer, there were no statistically significant differences in genotype distribution between gastric cancer cases and controls. This meta-analysis suggested that IL-10-592 allele polymorphism might be a risk factor for gastric cancer among Asians.
胃癌与 IL-10-592 多态性的关系报道结果不一致。本研究旨在定量评估 IL-10-592 等位基因多态性与胃癌易感性的关系。我们进行了广泛的相关研究检索,并进行了荟萃分析,包括 12 项研究,共 2285 例胃癌病例和 4236 例对照。基于所有研究的综合结果表明,胃癌病例与对照组之间基因型分布无显著差异,CC 与 CA/AA(OR=1.05,95%CI:0.92-1.18)、CC/CA 与 AA(OR=1.16,95%CI:0.92-1.46)、CC 与 CA(OR=1.03,95%CI:0.90-1.17)、CC 与 AA(OR=1.10,95%CI:0.90-1.34)和 CA 与 AA(OR=1.16,95%CI:0.92-1.45)。按种族分层时,发现亚洲人群中 CC/CA 与 AA 相比,胃癌病例的频率显著更高(OR=1.31,95%CI:1.08-1.59),CA 与 AA 相比,胃癌病例的频率也显著更高(OR=1.33,95%CI:1.09-1.63)。按胃癌的部位和 Lauren 分类分层时,胃癌病例与对照组之间基因型分布无统计学显著差异。本荟萃分析提示,IL-10-592 等位基因多态性可能是亚洲人群胃癌的危险因素。