Association study of MICA gene polymorphisms with rheumatoid arthritis susceptibility in south Tunisian population

作者：Achour Y; Kammoun A; Ben Hamad M; Mahfoudh N; Chaabane S; Marzouk S; Keskes L; Gaddour L; Bahloul Z; Maalej A^*

来源：International Journal of Immunogenetics, 2014, 41(6): 486-492.

DOI：10.1111/iji.12146

The aim of this study was to investigate the role of major histocompatibility complex (MHC) class I chain-related gene A (MICA) polymorphisms, important in natural killer (NK) cell function, in patients with rheumatoid arthritis (RA). A transmembrane (TM) alanine-encoding GCT repeats, termed A4, A5, A5.1, A6 and A9 in the MICA gene, and single-nucleotide polymorphisms (SNPs): the Met129Val polymorphism (rs1051792) and the nonsynonymously coding SNP (rs1051794) were genotyped in 142 patients with RA and 123 unrelated healthy individuals using, respectively, PCR fluorescent method, nested PCR-RFLP and allele specific PCR (ASP). Association was assessed based on the 2 test, genotype relative risk (GRR) and odds ratio (OR) with 95% confidence intervals (CIs). Our results show a trend of association of the different MICA genotypes G/G, G/A and A/A (P=0.029) which did not attain the significance after Bonferroni's correction (p(c)=0.08). Although, we revealed a significant association of the genotype A/A of MICA-250 in patients with RA compared to healthy controls (pc=0.033). In contrast, no significant differences between alleles and genotypes frequencies were found either with MICA-TM or MICA met129val (P>0.05) in our sample. Moreover, stratification of patients with RA according to clinical and immunological data for the different polymorphisms studied shows a significant association of both MICA-250G allele (pc=0.0075) and MICA-250 GG genotype (pc=0.008) and both allelic (val) (pc=0.021) and genotypic (val/val) distribution (p(c)=0.0095) for MICA met129val in the RF-positive subgroup compared to RF-negative patients with RA. In contrast, we found a strong association of the MICA-TM A9 allele in RF-negative patients with RA (p(c)=0.0003). This study indicates the involvement of the MICA-250 polymorphism in the genetic susceptibility and severity to RA and suggests that variations in MICA-TM and MICA met129val may have an effect on RA severity in our south Tunisian sample.

• 出版日期2014-12