Association between miR-146a rs2910164 polymorphism and autoimmune diseases susceptibility: A meta-analysis

被引:25
作者
Chen, Hui Fang [1 ]
Hu, Ting Ting [1 ]
Zheng, Xue Yan [1 ]
Li, Mei Qing [1 ]
Luo, Min Hong [1 ]
Yao, Yue Xian [1 ]
Chen, Qing [1 ]
Yu, Shou Yi [1 ]
机构
[1] Southern Med Univ, Sch Publ Hlth & Trop Med, Dept Epidemiol, Guangzhou, Guangdong, Peoples R China
关键词
Autoimmune diseases; miR-146a; rs2910164; Meta-analysis; SYSTEMIC-LUPUS-ERYTHEMATOSUS; RHEUMATOID-ARTHRITIS PATIENTS; IMMUNE CELL-DEVELOPMENT; MULTIPLE-SCLEROSIS; KINASE IRAK1; EXPRESSION; MICRORNA-146A; GENE; MIRNAS; TRIALS;
D O I
10.1016/j.gene.2013.03.073
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Published data on the rs2910164 in microRNA-146a (miR-146a) are shown to be associated with increased or decreased autoimmune diseases risk. To derive a more precise estimation of the relationship, we performed a meta-analysis to systematically summarize the possible. A meta-analysis including 11 studies with 3042 controls and 2197 cases was performed for genotypes CC (recessive effect), CC + CG (dominant effect) and C allele in fixed or random-effects models based on between-study heterogeneity. Overall, no significant association between miR-146a G/C rs2910164 polymorphism and autoimmune diseases risk was found in all genetic models when all studies were pooled into the meta-analysis. SLE (OR = 0.99, 95% CI: 0.90-1.10), RA (OR = 0.98, 95% CI: 0.85-1.14) did not yield statistical significance as for C allele pooled studies. In the subgroup analysis by ethnicity, still no significant association was detected in all genetic models. Our meta-analysis suggests that there is no association between miR-146a G/C rs2910164 polymorphism and the development of autoimmune diseases. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:259 / 264
页数:6
相关论文
共 41 条
[1]   miRNA in systemic lupus erythematosus [J].
Amarilyo, Gil ;
La Cava, Antonio .
CLINICAL IMMUNOLOGY, 2012, 144 (01) :26-31
[2]   Is there a common genetic basis for autoimmune diseases? [J].
Anaya, Juan-Manuel ;
Gomez, Luismiguel ;
Castiblanco, John .
CLINICAL & DEVELOPMENTAL IMMUNOLOGY, 2006, 13 (2-4) :185-195
[3]  
[Anonymous], 1997, LANCET
[4]   Impaired miR-146a expression links subclinical inflammation and insulin resistance in Type 2 diabetes [J].
Balasubramanyam, M. ;
Aravind, S. ;
Gokulakrishnan, K. ;
Prabu, P. ;
Sathishkumar, C. ;
Ranjani, H. ;
Mohan, V. .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2011, 351 (1-2) :197-205
[5]   MicroRNAs: new regulators of immune cell development and function [J].
Baltimore, David ;
Boldin, Mark P. ;
O'Connell, Ryan M. ;
Rao, Dinesh S. ;
Taganov, Konstantin D. .
NATURE IMMUNOLOGY, 2008, 9 (08) :839-845
[6]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[7]   OPERATING CHARACTERISTICS OF A BANK CORRELATION TEST FOR PUBLICATION BIAS [J].
BEGG, CB ;
MAZUMDAR, M .
BIOMETRICS, 1994, 50 (04) :1088-1101
[8]   The Role of microRNA-146a (miR-146a) and its Target IL-1R-Associated Kinase (IRAK1) in Psoriatic Arthritis Susceptibility [J].
Chatzikyriakidou, A. ;
Voulgari, P. V. ;
Georgiou, I. ;
Drosos, A. A. .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2010, 71 (05) :382-385
[9]   A polymorphism in the 3′-UTR of interleukin-1 receptor-associated kinase (IRAK1), a target gene of miR-146a, is associated with rheumatoid arthritis susceptibility [J].
Chatzikyriakidou, Anthoula ;
Voulgari, Paraskevi V. ;
Georgiou, Ioannis ;
Drosos, Alexandros A. .
JOINT BONE SPINE, 2010, 77 (05) :411-413
[10]  
Dai Y., 2011, LUPUS, V20, P1231