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miRNAs 基因多态性与关节炎的相关性:系统评价和荟萃分析。

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

机构信息

West China School of Nursing/West China Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China.

Key Laboratory of Birth Deficits and Related Diseases of Women and Children, West China Second Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China.

出版信息

Biosci Rep. 2019 Jul 18;39(7). doi: 10.1042/BSR20190298. Print 2019 Jul 31.

Abstract

To investigate whether microRNAs genes' polymorphisms are associated with arthritis. 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. 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. 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.

摘要

为了研究微小 RNA 基因多态性是否与关节炎有关。系统地检索了 PubMed、Cochrane Library 等数据库,以确定病例对照研究、系统评价和荟萃分析。使用固定效应模型或随机效应模型计算比值比(OR)和 95%置信区间(CI)。符合纳入标准的 22 项病例对照研究共纳入 10489 名参与者。miR-146a rs2910164(G/C)在任何模型中均与类风湿关节炎(RA)的发病风险无显著相关性。miR-146a rs2910164(G/C)与银屑病关节炎(PsA)的风险在杂合子模型和显性模型中存在显著相关性。杂合子模型显示 miR-146a rs2910164(G/C)多态性与强直性脊柱炎(AS)显著相关。miR-146a rs2910164(G/C)与幼年特发性关节炎(JRA)的发病风险在任何模型中均无显著相关性。此外,miR-499 rs3746444(T/C)在两个遗传模型中与 RA 的发病风险显著相关,且存在中度异质性。按种族亚组分析,在白种人群中,miR-499 rs3746444(T/C)与 RA 风险的任何模型均存在显著相关性,且无异质性。miR-146a rs2910164(G/C)与 RA 无相关性。miR-146a rs2910164(G/C)与 PsA 或 AS 显著相关。miR-499 rs3746444(T/C)与白种人群 RA 相关。这些发现不支持 miR-146a rs2910164(G/C)与 JRA 易感性之间的遗传相关性,以及 miR-196a-2 rs11614913(C/T)、miR-146a rs2431697、miR-146a rs57095329、miR-149 rs22928323 与关节炎之间的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19b8/6639462/fb2c7f0c1245/bsr-39-bsr20190298-g1.jpg

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