首页> 外文期刊>Gastroenterology research and practice >Association of Three Polymorphisms rs11614913, rs2910146, and rs3746444 in miRNA-196a2, miRNA-146a, and miRNA-499 with Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis
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Association of Three Polymorphisms rs11614913, rs2910146, and rs3746444 in miRNA-196a2, miRNA-146a, and miRNA-499 with Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis

机译:三种多态性RS11614913,RS2910146和RS3746444在MiRNA-196a2,miRNA-146a和miRNA-499中的三种多态性rs11146444具有炎性肠病疾病:系统评价和荟萃分析

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摘要

Background. It has been found that single-nucleotide polymorphisms (SNPs) of microRNA might be involved in the development of inflammatory bowel diseases (IBDs). However, the related retrospective research has not been reported. In this work, we performed a meta-analysis to derive a more precise estimation of the associated relationship. Methods. We searched the studies on the association of SNPs of microRNA with the hereditary susceptibility of IBD in PubMed and Embase; eligible research was selected by screening the abstract and full text. The meta-analysis was performed based on the statistical software Stata 14.0, and besides, the odds ratio and 95% confidence interval were calculated to evaluate the strength of the association. Results. 159 papers were acquired from the PubMed and Embase databases, and five eligible articles containing nine case-control studies were selected. In the study, we first found that the association between miRNA-196a2 rs11614913 and IBD was insignificant. Then, the susceptibility of miRNA-146a rs2910146 to IBD increased significantly in allelic comparison, homozygote model, heterozygote model, and dominant model. Moreover, a positive relationship between miRNA-499 rs3746444 and IBD was identified in the homozygote model. Conclusion. Our findings demonstrated that miRNA-146a rs2910146 (GC) polymorphism was associated with the susceptibility to IBD and miRNA-196a2 rs11614913 (TC) and miRNA-499 rs3746444 (AG) did not reveal an obvious relationship with the IBD susceptibility.
机译:背景。已经发现MicroRNA的单核苷酸多态性(SNP)可能参与炎症性肠病(IBDS)的发育。但是,尚未报告相关的回顾性研究。在这项工作中,我们执行了一个Meta分析,以推导出相关关系的更精确估计。方法。我们在PubMed and Embase中搜索了MicroRNA的SNP与遗传敏感性的研究的研究;通过筛选摘要和全文来选择合格的研究。基于统计软件STATA 14.0,除此之外,计算荟萃分析,计算差距和95%置信区间以评估结合的强度。结果。从PubMed和Embase数据库中获得了159篇论文,并选择了五种含有九种病程控制研究的符合条件的文章。在该研究中,我们首先发现MiRNA-196A2 RS11614913和IBD之间的关联是微不足道的。然后,在等位基因比较,Homozygote模型,杂合子模型和显性模型中,MiRNA-146A RS2910146至IBD的敏感性显着增加。此外,在Homozygote模型中鉴定了MiRNA-499 RS3746444和IBD之间的阳性关系。结论。我们的研究结果表明,miRNA-146A RS2910146(G> C)多态性与IBD和MiRNA-196A2 RS11614913(T> C)和MiRNA-499 RS3746444(A> G)与IBD的关系没有透露易感性。

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    Jilin Univ Hosp 2 Dept Gen Surg Changchun Jilin Peoples R China;

    Jilin Univ Sch Pharmaceut Sci Changchun Jilin Peoples R China;

    Jilin Univ Hosp 2 Dept Gen Surg Changchun Jilin Peoples R China;

    Jilin Univ Sch Pharmaceut Sci Changchun Jilin Peoples R China;

    Jilin Univ Hosp 2 Dept Gen Surg Changchun Jilin Peoples R China;

    South China Univ Technol Sch Business Adm Guangzhou Guangdong Peoples R China;

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  • 正文语种 eng
  • 中图分类 消化系及腹部疾病;
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