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首页> 外文期刊>International journal of immunogenetics >Association study of MICA gene polymorphisms with rheumatoid arthritis susceptibility in south Tunisian population
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Association study of MICA gene polymorphisms with rheumatoid arthritis susceptibility in south Tunisian population

机译:突尼斯南部人群MICA基因多态性与类风湿关节炎易感性的关联研究

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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.
机译:这项研究的目的是调查类风湿性关节炎(RA)患者的主要组织相容性复合体(MHC)I类链相关基因A(MICA)多态性对自然杀伤(NK)细胞功能的重要作用。跨膜(TM)编码丙氨酸的GCT重复序列,在MICA基因中称为A4,A5,A5.1,A6和A9,以及单核苷酸多态性(SNP):Met129Val多态性(rs1051792)和非同义编码SNP(rs1051794分别使用PCR荧光法,巢式PCR-RFLP和等位基因特异性PCR(ASP)对142例RA患者和123例无关健康个体进行基因分型。基于2个测试,基因型相对风险(GRR)和比值比(OR)和95%置信区间(CIs)对关联进行评估。我们的结果表明,不同的MICA基因型G / G,G / A和A / A的关联趋势(P = 0.029)在Bonferroni校正后没有达到显着性(p(c)= 0.08)。虽然,我们发现与健康对照组相比,RA患者中MICA-250的A / A基因型显着相关(pc = 0.033)。相反,在我们的样本中,MICA-TM或MICA met129val的等位基因和基因型频率之间没有发现显着差异(P> 0.05)。此外,根据临床和免疫学数据对所研究的不同多态性对RA患者进行的分层显示,MICA-250G等位基因(pc = 0.0075)和MICA-250 GG基因型(pc = 0.008)和两个等位基因(val)均存在显着关联与RF阴性的RA患者相比,MICA met129val的MICA(pc = 0.021)和基因型(val / val)分布(p(c)= 0.0095)。相反,我们在RA的RF阴性患者中发现了MICA-TM A9等位基因有很强的关联性(p(c)= 0.0003)。这项研究表明,MICA-250基因多态性与RA的遗传易感性和严重程度有关,并表明在我们的突尼斯南部样本中,MICA-TM和MICA met129val的变异可能对RA的严重程度产生影响。

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