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首页> 外文期刊>Arthritis and Rheumatism >A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians
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A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians

机译:全基因组关联研究揭示了北印度人类风湿关节炎的新型非HLA易感性基因ARL15

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摘要

Objective: Genome-wide association studies (GWAS) and their subsequent meta-analyses have changed the landscape of genetics in rheumatoid arthritis (RA) by uncovering several novel genes. Such studies are heavily weighted by samples from Caucasian populations, but they explain only a small proportion of total heritability. Our previous studies in genetically distinct North Indian RA cohorts have demonstrated apparent allelic/genetic heterogeneity between North Indian and Western populations, warranting GWAS in non-European populations. We undertook this study to detect additional disease-associated loci that may be collectively important in the presence or absence of genes with a major effect. Methods: High-quality genotypes for 600,000 single-nucleotide polymorphisms (SNPs) in 706 RA patients and 761 controls from North India were generated in the discovery stage. Twelve SNPs showing suggestive association (P 5 × 10-5) were then tested in an independent cohort of 927 RA patients and 1,148 controls. Additional disease-associated loci were determined using support vector machine (SVM) analyses. Fine-mapping of novel loci was performed by using imputation. Results: In addition to the expected association of the HLA locus with RA, we identified association with a novel intronic SNP of ARL15 (rs255758) on chromosome 5 (Pcombined = 6.57 × 10 -6; odds ratio 1.42). Genotype-phenotype correlation by assaying adiponectin levels demonstrated the functional significance of this novel gene in disease pathogenesis. SVM analysis confirmed this association along with that of a few more replication stage genes. Conclusion: In this first GWAS of RA among North Indians, ARL15 emerged as a novel genetic risk factor in addition to the classic HLA locus, which suggests that population-specific genetic loci as well as those shared between Asian and European populations contribute to RA etiology. Furthermore, our study reveals the potential of machine learning methods in unraveling gene-gene interactions using GWAS data.
机译:目的:全基因组关联研究(GWAS)及其后续的荟萃分析通过发现一些新基因,改变了类风湿关节炎(RA)的遗传学格局。这些研究在高加索人群中获得了很大的权重,但它们仅解释了总遗传力的一小部分。我们先前在遗传上不同的北印度RA队列研究表明,北印度和西方人群之间存在明显的等位基因/遗传异质性,因此有必要在非欧洲人群中使用GWAS。我们进行了这项研究,以检测其他与疾病相关的基因座,这些基因座在存在或不存在具有重大影响的基因时可能共同重要。方法:在发现阶段,产生了来自印度北部的706名RA患者和761名对照的> 600,000个单核苷酸多态性(SNP)的高质量基因型。然后在927名RA患者和1,148名对照的独立队列中测试了十二个提示性关联的SNP(P <5×10-5)。使用支持向量机(SVM)分析确定了其他与疾病相关的基因座。新的基因座的精细映射是通过使用插补进行的。结果:除了预期的HLA基因座与RA的关联外,我们还鉴定了与5号染色体上ARL15的新型内含子SNP(rs255758)的关联(组合= 6.57×10 -6;优势比1.42)。通过检测脂联素水平的基因型与表型相关性证明了该新基因在疾病发病机理中的功能意义。 SVM分析证实了这种关联以及更多复制阶段基因的关联。结论:在北印第安人中,RA的第一个GWAS中,除了经典的HLA基因座外,ARL15还作为一种新的遗传危险因素出现,这表明特定人群的遗传基因座以及亚洲和欧洲人群之间共有的基因座也有助于RA的病因学。此外,我们的研究揭示了使用GWAS数据揭示机器学习方法在揭示基因与基因相互作用中的潜力。

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