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首页> 外文期刊>International journal of immunogenetics >Associative role of HLA-DRB1 SNP genotypes as risk factors for susceptibility and severity of rheumatoid arthritis: A North-east Indian population-based study
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Associative role of HLA-DRB1 SNP genotypes as risk factors for susceptibility and severity of rheumatoid arthritis: A North-east Indian population-based study

机译:HLA-DRB1 SNP基因型作为类风湿性关节炎易感性和严重程度的危险因素的关联作用:基于东北印度人的研究

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Rheumatoid arthritis (RA) is a complex, multifactorial, systemic autoimmune disease. Reports are suggestive of the role of HLA especially HLA-DRB1 alterations in RA pathogenesis. Existing data involving different geographical populations on the role of alterations in specific locus of HLA-DRB1 in RA susceptibility and severity are equivocal, with no data available from ethnically distinct North-east Indian population, where RA cases are alarmingly increasing. This study aimed to evaluate the association of HLA-DRB1 gene SNPs (rs13192471, rs660895 and rs6457617) with susceptibility and severity of RA in an ethnically distinct North-east Indian population. Whole blood was collected from clinically characterized RA cases (satisfying the American College of Rheumatology 1987 criteria) (n=123) and community-based age and sex-matched healthy controls (n=156) with informed consent. The HLA-DRB1 SNP analysis was performed for all the RA and control cases using ARMS-PCR using case and control genomic DNA as template. Statistical analysis was performed by SPSSv13.0 software. The HLA-DRB1 rs660895 showed both wild (AA) and heterozygote (AG) genotype but the heterozygote allele was found to be associated with reduced risk of RA compared to controls [OR=0.531, p=.024]. The difference in distribution of rs6457617 polymorphism between RA and control cases was comparable [OR=0.525, p=.079]. Significantly higher distribution of variant rs13192471 genotype was observed in RA cases (69.92%) compared to controls (46.75%) (p.001) and was associated with increased risk of susceptibility to RA [OR=2.576, p.001] compared to controls, as well as progression to severity in RA cases [OR=2.404, p=.048]. Combinatorially also, the presence of rs13192471 variant genotype was associated with increased risk of RA susceptibility [OR=8.267, p=.026] and RA severity [OR=3.647, p=.280]. Alterations in HLA-DRB1 are associated with RA susceptibility. HLA-DRB1 rs13192471 SNP plays a critical role in RA susceptibility and severity in North-east Indian cases and has prognostic significance in RA.
机译:类风湿性关节炎(RA)是一种复杂,多因素,全身自身免疫疾病。报告旨在提示HLA尤其是RA发病机制中的HLA-DRB1改变的作用。涉及不同地理群体的现有数据对RA易感性和严重程度的HLA-DRB1特定轨迹的改变的作用是等偶数的,没有任何基于西北印度人群可获得的数据,其中RA病例令人惊讶地增加。本研究旨在评估HLA-DRB1基因SNP(RS13192471,RS660895和RS6457617)的关联,在广泛的东北印度人口中的敏感性和严重程度。从临床表征的RA病例(满足美国风湿病学院校的标准)(n = 123)和社区年龄和性别匹配的健康控制(n = 156),从临床表征中收集了全血。使用案例和对照基因组DNA作为模板对所有RA和控制病例进行HLA-DRB1 SNP分析。 SPSSv13.0软件执行统计分析。 HLA-DRB1 RS660895显示野生(AA)和杂合子(AG)基因型,但发现与对照[或= 0.531,p = .024]相比,杂合子等位基因与Ra的风险降低相关。 RA和控制壳体之间的Rs6457617多态性的分布差异是可比的[或= 0.525,p = .079]。在RA病例(69.92%)与对照(46.75%)(P <0.001)相比,在RA病例(69.92%)中观察到显着较高的变异RS13192471基因型,并且与Ra [或= 2.576,P& .001]的易感性的风险增加相关控制,以及RA病例中的严重性的进展[或= 2.404,p = .048]。组合也,RS13192471变体基因型的存在与Ra敏感性的风险增加有关[或= 8.267,p = .026]和Ra严重性[或= 3.647,p = .280]。 HLA-DRB1中的改变与RA易感性有关。 HLA-DRB1 RS13192471 SNP在东北印度病例的RA易感性和严重程度中发挥着关键作用,在RA中具有预后意义。

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