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

Author:

Xiao Yingqi1,Liu Hui2,Chen Li3,Wang Yang4,Yao Xiang5,Jiang Xiaolian1

Affiliation:

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

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

3. Department of Orthopedics, West China Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China

4. Research Department, Childrens Hospital of Chongqing Medical University, Chongqing 401147, China

5. Department of Radiology, The Xiangan Hospital of Xia Men University, Xiamen 361101, Fujian Province, China

Abstract

Abstract 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.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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