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Association of microRNAs genes polymorphisms with arthritis: a systematic review and meta-analysis

机译:microRNA基因多态性与关节炎的关联:系统评价和荟萃分析

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摘要

>Objective: To investigate whether microRNAs genes’ polymorphisms are associated with arthritis. >Methods: The PubMed, Cochrane Library et al. were systematically searched to identify case–control studies, systematic reviews and meta-analyses. A meta-analysis was performed to calculate odds ratios (ORs), and confidence intervals (CIs) at 95% using fixed-effect model or random-effects model. >Results: Twenty-two case–control studies involving 10489 participants fulfilled the inclusion criteria. MiR-146a rs2910164 (G/C) was not significantly associated with the risk of rheumatoid arthritis (RA) in any model. Significant associations were found between miR-146a rs2910164 (G/C) and the risk of psoriatic arthritis (PsA) in the heterozygous model and the dominant model. The heterozygous model showed a significant association between the miR-146a rs2910164 (G/C) polymorphism and ankylosing spondylitis (AS). And there was no significant association of miR-146a rs2910164 (G/C) with risk of juvenile rheumatoid arthritis (JRA) at any model. Additionally, there was a significant association of miR-499 rs3746444 (T/C) with risk of RA at two genetic models, and with a moderate heterogeneity. When subgroup analysis by ethnicity, significant associations were almost found between miR-499 rs3746444 (T/C) and the risk of RA in any model in Caucasian populations, and there is no heterogeneity. >Conclusions: The association of miR-146a rs2910164 (G/C) with RA was not found. And there was a significant association between miR-146a rs2910164(G/C) and PsA or AS. MiR-499 rs3746444 (T/C) was associated with RA in Caucasian populations. These findings did not support the genetic association between miR-146a rs2910164 (G/C) and JRA susceptibility, as well as the association of miR-196a-2 rs11614913 (C/T), miR-146a rs2431697, miR-146a rs57095329, miR-149 rs22928323 with arthritis.
机译:>目的:研究microRNA基因的多态性是否与关节炎有关。 >方法: PubMed,Cochrane图书馆等。进行系统搜索以识别病例对照研究,系统评价和荟萃分析。使用固定效应模型或随机效应模型进行荟萃分析,以计算95%的比值比(OR)和置信区间(CIs)。 >结果:涉及10489名参与者的22例病例对照研究符合纳入标准。在任何模型中,MiR-146a rs2910164(G / C)与类风湿关节炎(RA)的风险均无显着相关性。在杂合模型和显性模型中,发现miR-146a rs2910164(G / C)与银屑病关节炎(PsA)风险之间存在显着关联。杂合模型显示miR-146a rs2910164(G / C)多态性与强直性脊柱炎(AS)之间存在显着关联。而且在任何模型中,miR-146a rs2910164(G / C)与青少年类风湿关节炎(JRA)的风险均无显着关联。此外,在两种遗传模型中,miR-499 rs3746444(T / C)与RA风险显着相关,并且具有中等异质性。通过种族进行亚组分析时,在白种人模型中的任何模型中,miR-499 rs3746444(T / C)与RA风险之间几乎都存在显着关联,并且没有异质性。 >结论:未发现miR-146a rs2910164(G / C)与RA的关联。而且miR-146a rs2910164(G / C)与PsA或AS之间存在显着关联。在白种人人群中,MiR-499 rs3746444(T / C)与RA相关。这些发现不支持miR-146a rs2910164(G / C)与JRA易感性之间的遗传关联,也不支持miR-196a-2 rs11614913(C / T),miR-146a rs2431697,miR-146a rs57095329,患有关节炎的miR-149 rs22928323。

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