首页> 外文期刊>Journal of genetics >Analysis of two susceptibility SNPs in HLA region and evidence of interaction between rs6457617 in HLA-DQB1 and HLA-DRB1*04 locus on Tunisian rheumatoid arthritis
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Analysis of two susceptibility SNPs in HLA region and evidence of interaction between rs6457617 in HLA-DQB1 and HLA-DRB1*04 locus on Tunisian rheumatoid arthritis

机译:HLA-DQB1和HLA-DRB1 * 04位于突尼斯类风湿性关节炎的HLA区域中两个易感性SNP的分析及rs6457617 rs6457617之间的综合证据

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Previous genomewide association studies (GWAS) and meta-analyses have enumerated several genes/loci in major histocompatibility complex region, which are consistently associated with rheumatoid arthritis (RA) in different ethnic populations. Given the genetic heterogeneity of the disease, it is necessary to replicate these susceptibility loci in other populations. In this case, we investigate the analysis of two SNPs, rs13192471 and rs6457617, from the human leukocyte antigen (HLA) region with the risk of RA in Tunisian population. These SNPs were previously identified to have a strong RA association signal in several GWAS studies. A case-control sample composed of 142 RA patients and 123 healthy controls was analysed. Genotyping of rs13192471 and rs6457617 was carried out using real-time PCR methods by TaqMan allelic discrimination assay. A trend of significant association was found in rs6457617 TT genotype with susceptibility to RA (, , ). Moreover, using multivariable analysis, the combination of rs6457617*TT-HLA-DRB1* increased risk of RA (), which suggest a gene-gene interaction event between rs6457617 located within the HLA-DQB1 and HLA-DRB1. Additionally, haplotypic analysis highlighted a significant association of rs6457617*T-HLA-DRB1* haplotype with susceptibility to RA (, , ). An evidence of association was shown subsequently in subgroup with rs6457617 both in T allele and TT genotype (, , and , , , respectively). However, no association was shown for rs13192471 polymorphism with susceptibility and severity to RA. This study suggests the involvement of rs6457617 locus as risk variant for susceptibility/severity to RA in Tunisian population. Secondly, it highlights the gene-gene interaction between HLA-DQB1 and HLA-DRB1.
机译:先前的基因组结合研究(GWAS)和荟萃分析列在主要组织相容性复杂区中的几个基因/基因座,其与不同种族群体中的类风湿性关节炎(RA)一致。鉴于疾病的遗传异质性,有必要在其他群体中复制这些易感性基因座。在这种情况下,我们研究了来自人白细胞抗原(HLA)区域的两个SNP,RS13192471和RS6457617的分析,突尼斯人口中的RA风险。先前,这些SNP已经识别出在几个GWAS研究中具有强烈的RA关联信号。分析了由142例患者和123例健康对照组成的病例对照样品。使用Taqman等位基因辨别测定法使用实时PCR方法进行RS13192471和RS6457617的基因分型。在RS6457617 TT基因型中发现了一个重要关联的趋势,对Ra(,)易感性。此外,使用多变量分析,RS6457617 * TT-HLA-DRB1 *的组合增加了RA()的风险,这表明位于HLA-DQB1和HLA-DRB1内的RS6457617之间的基因基因相互作用事件。此外,单倍型分析强调了RS6457617 * T-HLA-DRB1 *单倍型的显着关联,易受RA(,)的易感性。随后在T visele和TT基因型中的亚组中显示了关联的证据,其副组和TT基因型(以及分别)。然而,对于Rs13192471多态性没有任何关联,易感性和严重程度对Ra。本研究表明RS6457617基因座作为突尼斯人群中RA的易感性/严重程度的风险变量。其次,它突出了HLA-DQB1和HLA-DRB1之间的基因基因相互作用。

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