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Association between polymorphisms in microRNAs and susceptibility to diabetes mellitus: A meta-analysis

机译:MicroRNA中多态性与糖尿病易感性的关系:META分析

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Background: Accumulated evidence has indicated the associations between single-nucleotide polymorphisms (SNPs) in microRNAs (miRNAs) and the susceptibility to diabetes mellitus (DM), but the conclusions remain controversial. This study was to investigate the true contribution of miRNA SNPs to the risk of DM by using a meta-analysis of all the published studies. Methods: Relevant studies were identified in the databases of PubMed and the Cochrane Library databases. The strength of associations between miRNA polymorphisms and DM risk was assessed by odds ratios (ORs) and 95% confidence intervals (95% CIs) under five genetic models using the STATA software. Results: Six studies, containing 2773 cases and 2632 controls, were enrolled, 5 of which evaluated miR-146a (rs2910164), 4 for miR-27a (rs895819), and 3 for miR-124 (rs531564) and 2 for miR-375 (rs6715345), miR-128a (rs11888095), miR-194a (rs3820455). The meta-analysis indicated that the G allele or GG genotype of miR-146a rs2910164 was associated with a significantly increased risk for DM compared with C allele or GC/CC genotype in Latin American population; CC genotype of miR-27a rs895819 polymorphism was associated with a significantly decreased risk for DM in Asian population compared with the TT genotype; patients carrying with CC genotype of miR-124 rs531564 had a lower probability to develop DM regardless of ethnicity; no associations were identified between polymorphisms in miR-375, miR-128a, miR-194a and the susceptibility to DM. Conclusion: Our study suggests that miR-146a/miR-27a and miR-124 polymorphisms may be ethnicity-dependent or -independent susceptibility factors to DM, respectively.
机译:背景:累积证据表明单核苷酸多态性(SNP)在microRNA(miRNA)和对糖尿病(DM)的易感性之间的关联,但结论仍然存在争议。本研究是通过使用所有公布研究的META分析来研究MiRNA SNP对DM风险的真实贡献。方法:在PubMed和Cochrane库数据库的数据库中确定了相关研究。 MiRNA多态性和DM风险之间的关联强度由使用STATA软件的五个遗传模型下的差异比率(或)和95%置信区间(95%CIs)评估。结果:六项研究,含有2773例和2632种对照,其中5例,其中5个评估MiR-146a(RS2910164),4个用于miR-27a(RS895819),4个用于miR-124(Rs531564)和miR-375的2个(RS6715345),MIR-128A(RS11888095),MIR-194A(RS3820455)。 Meta分析表明MiR-146A RS2910164的G等位基因或GG基因型与拉丁美洲人口的C等位基因或GC / CC基因型相比,DM的风险显着增加; MiR-27A RS895819多态性的CC基因型与TT基因型相比,亚洲人群中DM的风险显着降低有关;患有MIR-124 rs531564的CC基因型的患者具有较低的概率,无论种族如何发展DM; miR-375,miR-128a,miR-194a的多态性之间没有鉴定关联和对DM的敏感性。结论:我们的研究表明,MIR-146A / MIR-27A和MIR-124多态性分别可以分别对DM的种族依赖性或依赖性敏感因素。

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