Predisposition to Behçet’s disease and VKH syndrome by genetic variants of miR-182

• Published in: Journal of molecular medicine (Berlin, Germany) Vol. 92; no. 9; pp. 961 - 967
• Main Authors: Yu, Hongsong, Liu, Yunjia, Bai, Lin, Kijlstra, Aize, Yang, Peizeng
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.09.2014; Springer Nature B.V
• Subjects: Behcet Syndrome - genetics; Biomedical and Life Sciences; Biomedicine; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Human Genetics; Humans; Internal Medicine; MicroRNAs - genetics; Molecular Medicine; Original Article; Polymorphism, Single Nucleotide; Uveomeningoencephalitic Syndrome - genetics; miR-182; miR-27a; Behçet’s disease; Vogt–Koyanagi–Harada syndrome; IL2RA; FoxO1
• ISSN: 0946-2716; 1432-1440
• DOI: 10.1007/s00109-014-1159-9

Previous studies have identified miR-182 , miR-27a , FoxO1 , and IL2RA as regulatory factors for Treg cell development and function. In order to investigate the association of miR-182, miR-27a, FoxO1 , and IL2RA gene polymorphisms with Behçet’s disease (BD) and Vogt–Koyanagi–Harada (VKH) syndrome in a Chinese Han population, a two-stage association study was performed in 820 BD, 900 VKH patients, and 1,800 controls using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) assay. In the first stage study, association analysis of 10 single nucleotide polymorphisms (SNPs) was performed in 400 BD, 400 VKH patients, and 600 controls. The results showed significantly decreased frequencies of the miR-182/rs76481776 CC genotype and C allele in BD ( P  = 3.36 × 10 −4 , OR = 0.55; P  = 4.74 × 10 −4 , OR = 0.59) and VKH patients ( P  = 1.11 × 10 −4 , OR = 0.53; P  = 1.26 × 10 −4 , OR = 0.56). No significant association of the other nine SNPs with BD or VKH was observed. In the second stage study, association analysis of miR-182/rs76481776 was performed in 420 BD, 500 VKH patients, and 1,200 controls. The second stage and combined studies confirmed the association of miR-182/rs76481776 with BD (CC genotype: P  = 3.25 × 10 −7 , OR = 0.58; C allele: P  = 1.81 × 10 −7 , OR = 0.60) and VKH (CC genotype: P  = 7.89 × 10 −8 , OR = 0.57; C allele: P  = 2.52 × 10 −8 , OR = 0.59). Real-time PCR analysis showed a significantly increased expression of miR-182 in TT/CT cases compared to CC cases in anti-CD3/CD28 antibodies-stimulated CD4 + T cells ( P  = 2.1 × 10 −2 ). In conclusion, this study suggests that miR-182, but not miR-27a, FoxO1 , and IL2RA , contributes to the genetic susceptibility of BD and VKH. Key Message MiR-182 contributes to genetic susceptibility of BD and VKH. No significant association of miR-27a, FoxO1, and IL2RA with BD or VKH was observed. Significantly increased expression of miR-182 in TT/CT cases compared to CC cases was observed.