Park Robin, Lee Won Jin, Ji Jong Dae
a Division of Rheumatology , College of Medicine, Korea University , Seoul , Korea and.
b Department of Preventive Medicine , College of Medicine, Korea University , Seoul , South Korea.
Autoimmunity. 2016 Nov;49(7):451-458. doi: 10.3109/08916934.2016.1171854. Epub 2016 Apr 20.
Studies suggest associations between the miR-146a single nucleotide polymorphisms (SNPs) and susceptibility to autoimmune diseases. However, the results are inconsistent and inconclusive. Therefore, the aim of this study was to arrive at a conclusion about the association between the three functional miR-146a SNPs and autoimmune disease risk. Studies were identified through PubMed/MEDLINE searches for studies published up to January 2016 using as keywords rs2910164, rs57095329, rs2431697, and miR-146a polymorphisms. Thirty studies were included in the meta-analysis. The SNP rs2910164 G > C was found to be associated with increased risk of multiple sclerosis (CC + CG versus GG, OR = 1.25, 95% CI: 1.01-1.55), with decreased risks of psoriasis (C versus G, OR = 0.81, 95% CI: 0.69-0.96; CC versus GC + GG, OR = 0.73, 95% CI: 0.56-0.94), Behcet's disease (CC versus GC + GG, OR = 0.60, 95% CI: 0.50-0.73), asthma (C versus G, OR = 0.80, 95% CI: 0.69-0.93; CC versus GC + GG, OR = 0.65, 95% CI: 0.48-0.86), and uveitis (CC + CG versus GG, OR = 0.61, 95% CI: 0.49-0.77). The SNP rs2431697 C > T was found to be associated with an increased risk of SLE (T versus C, OR = 1.26, 95% CI: 1.15-1.38; TC + TT versus CC, OR = 1.28, 95% CI: 1.03-1.58; TT versus TC + CC, OR = 1.40, 95% CI: 1.21-1.62). The SNP rs57095329 A > G was found to be associated with an increased risk of SLE (G versus C, OR = 1.25, 95% CI: 1.17-1.35). The miR-146a SNPs rs2910164, rs57095329, rs2431697 are associated with susceptibility to certain autoimmune diseases. However, for other autoimmune diseases, they may be protective or insignificant.
研究表明,微小RNA-146a单核苷酸多态性(SNP)与自身免疫性疾病易感性之间存在关联。然而,结果并不一致且尚无定论。因此,本研究的目的是就三个功能性微小RNA-146a SNP与自身免疫性疾病风险之间的关联得出结论。通过PubMed/MEDLINE检索截至2016年1月发表的研究,使用rs2910164、rs57095329、rs2431697和微小RNA-146a多态性作为关键词。30项研究纳入荟萃分析。发现SNP rs2910164 G > C与多发性硬化症风险增加相关(CC + CG与GG相比,OR = 1.25,95%CI:1.01 - 1.55),与银屑病风险降低相关(C与G相比,OR = 0.81,95%CI:0.69 - 0.96;CC与GC + GG相比,OR = 0.73,95%CI:0.56 - 0.94)、白塞病(CC与GC + GG相比,OR = 0.60,95%CI:0.50 - 0.73)、哮喘(C与G相比,OR = 0.80,95%CI:0.69 - 0.93;CC与GC + GG相比,OR = 0.65,95%CI:0.48 - 0.86)和葡萄膜炎(CC + CG与GG相比,OR = 0.61,95%CI:0.49 - 0.77)。发现SNP rs2431697 C > T与系统性红斑狼疮风险增加相关(T与C相比,OR = 1.26,95%CI:1.15 - 1.38;TC + TT与CC相比,OR = 1.28,95%CI:1.03 - 1.58;TT与TC + CC相比,OR = 1.40,95%CI:1.21 - 1.62)。发现SNP rs57095329 A > G与系统性红斑狼疮风险增加相关(G与C相比,OR = 1.25,95%CI:1.17 - 1.35)。微小RNA-146a SNP rs2910164、rs57095329、rs2431697与某些自身免疫性疾病易感性相关。然而,对于其他自身免疫性疾病,它们可能具有保护作用或无显著意义。