Qian Bao-Xin, Ye Qing, Zhao Xin-Yu, Han Tao, Wang Feng-Mei, Yang Jie
1 School of Basic Medical Sciences, Tianjin Medical University , Tianjin, P.R. China .
2 Research Center of Basic Medical Science, Tianjin Medical University , Tianjin, P.R. China .
Genet Test Mol Biomarkers. 2018 May;22(5):302-313. doi: 10.1089/gtmb.2018.0010. Epub 2018 Apr 25.
Single nucleotide polymorphisms of the IL10 gene have been linked to the occurrence of autoimmune liver disease.
We performed a meta-analysis to assess the association between three IL10 promoter polymorphisms (rs1800896, rs1800871, and rs1800872) and the risk of autoimmune hepatitis, primary biliary cholangitis, and primary sclerosing cholangitis.
In total, 1420 articles were initially identified through database retrieval. After screening, seven eligible articles were ultimately included in the meta-analysis. A fixed-effect model was used for all Mantel-Haenszel statistics due to the absence of large between-study heterogeneity (all I < 50%, p > 0.1). No association between any of the studied polymorphisms and risk of autoimmune liver disease was detected in the allele, homozygote, heterozygote, dominant, recessive, or carrier genetic models (p > 0.05). Potential publication bias was excluded using Begg's and Egger's tests. Similar negative results were observed in subgroup analyses and in an analysis of the three haplotypes of rs1800896/rs1800871/rs1800872 (G/C/C, A/C/C, and A/T/A).
Our meta-analysis strongly suggests that the IL10 rs1800896, rs1800871, and rs1800872 polymorphisms are not associated with the risk of autoimmune liver disease.
白细胞介素10(IL10)基因的单核苷酸多态性与自身免疫性肝病的发生有关。
我们进行了一项荟萃分析,以评估三种IL10启动子多态性(rs1800896、rs1800871和rs1800872)与自身免疫性肝炎、原发性胆汁性胆管炎和原发性硬化性胆管炎风险之间的关联。
通过数据库检索,最初共识别出1420篇文章。经过筛选,最终有7篇符合条件的文章被纳入荟萃分析。由于研究间不存在较大异质性(所有I<50%,p>0.1),所有Mantel-Haenszel统计均采用固定效应模型。在等位基因、纯合子、杂合子、显性、隐性或携带者遗传模型中,未检测到任何研究的多态性与自身免疫性肝病风险之间存在关联(p>0.05)。使用Begg检验和Egger检验排除了潜在的发表偏倚。在亚组分析以及对rs1800896/rs1800871/rs1800872的三种单倍型(G/C/C、A/C/C和A/T/A)的分析中也观察到了类似的阴性结果。
我们的荟萃分析有力地表明,IL10基因的rs1800896、rs1800871和rs1800872多态性与自身免疫性肝病风险无关。