Shan-Yu Qin, Hai-Xing Jiang, Dong-Hong Lu, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
World J Gastroenterol. 2013 Dec 28;19(48):9472-80. doi: 10.3748/wjg.v19.i48.9472.
To clarify the current understanding of the association between interleukin-10 (IL-10) polymorphisms and the risk of irritable bowel syndrome (IBS).
We searched for studies in any language recorded in PubMed, Embase and Cochrane library before August 2013. The associations under allele contrast model, codominant model, dominant model, and recessive model were analyzed. The strengths of the association between IL-10 polymorphisms and IBS risk were estimated using odds ratios (OR) with 95% confidence interval (CI). Fixed effects model was used to pool the result if the test of heterogeneity was not significant, otherwise the random-effect model was selected.
Eight case-control studies analyzing three single-nucleotide polymorphisms rs1800870 (-1082 A/G), rs1800871 (-819C/T), and rs1800872 (-592A/C) of the IL-10 gene, which involved 928 cases and 1363 controls, were eligible for our analysis. The results showed that rs1800870 polymorphisms were associated with a decreased risk of IBS (GG+GA vs AA: OR = 0.80, 95%CI: 0.66-0.96), (AA+GA vs GG: OR = 0.68, 95%CI: 0.52-0.90). Subgroup analysis revealed such association only existed in Caucasian ethnicity (AA+GA vs GG, OR = 0.70, 95%CI: 0.55-0.89). The rs1800872 polymorphisms were associated with an increased risk of IBS in Asian ethnicity (CC vs GG: OR = 1.29, 95%CI: 1.01-1.16). There were no associations between rs1800871 polymorphisms and the IBS risk.
The results suggest that IL-10 rs1800870 confers susceptibility to the risk of IBS in Caucasian ethnicity, and the rs1800872 may associate with IBS risk in Asians. However, no significant associations are found between rs1800871 and IBS risk.
阐明白细胞介素-10(IL-10)多态性与肠易激综合征(IBS)风险之间的关联。
我们检索了 2013 年 8 月前在 PubMed、Embase 和 Cochrane 图书馆中收录的任何语言的研究。分析了等位基因对比模型、共显性模型、显性模型和隐性模型下的相关性。使用优势比(OR)及其 95%置信区间(CI)来估计 IL-10 多态性与 IBS 风险之间的关联强度。如果异质性检验不显著,则采用固定效应模型进行合并;否则采用随机效应模型。
纳入了 8 项病例对照研究,共分析了白细胞介素 10 基因的 3 个单核苷酸多态性 rs1800870(-1082 A/G)、rs1800871(-819C/T)和 rs1800872(-592A/C),共涉及 928 例病例和 1363 例对照。结果表明,rs1800870 多态性与 IBS 风险降低相关(GG+GA 与 AA:OR=0.80,95%CI:0.66-0.96),(AA+GA 与 GG:OR=0.68,95%CI:0.52-0.90)。亚组分析显示,这种相关性仅存在于白种人群中(AA+GA 与 GG,OR=0.70,95%CI:0.55-0.89)。rs1800872 多态性与亚洲人群的 IBS 风险增加相关(CC 与 GG:OR=1.29,95%CI:1.01-1.16)。rs1800871 多态性与 IBS 风险无相关性。
结果表明,IL-10 rs1800870 赋予白种人群患 IBS 的易感性,rs1800872 可能与亚洲人群的 IBS 风险相关。然而,rs1800871 与 IBS 风险之间无显著相关性。