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高密度遗传图谱分析确定类风湿关节炎的新易感位点。

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis.

机构信息

Arthritis Research UK Epidemiology Unit, Centre for Musculoskeletal Research, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.

出版信息

Nat Genet. 2012 Dec;44(12):1336-40. doi: 10.1038/ng.2462. Epub 2012 Nov 11.

Abstract

Using the Immunochip custom SNP array, which was designed for dense genotyping of 186 loci identified through genome-wide association studies (GWAS), we analyzed 11,475 individuals with rheumatoid arthritis (cases) of European ancestry and 15,870 controls for 129,464 markers. We combined these data in a meta-analysis with GWAS data from additional independent cases (n = 2,363) and controls (n = 17,872). We identified 14 new susceptibility loci, 9 of which were associated with rheumatoid arthritis overall and five of which were specifically associated with disease that was positive for anticitrullinated peptide antibodies, bringing the number of confirmed rheumatoid arthritis risk loci in individuals of European ancestry to 46. We refined the peak of association to a single gene for 19 loci, identified secondary independent effects at 6 loci and identified association to low-frequency variants at 4 loci. Bioinformatic analyses generated strong hypotheses for the causal SNP at seven loci. This study illustrates the advantages of dense SNP mapping analysis to inform subsequent functional investigations.

摘要

我们使用了 Immunochip 定制 SNP 芯片,该芯片是专门为通过全基因组关联研究(GWAS)鉴定的 186 个基因座的高密度基因分型而设计的,对 11475 名欧洲血统的类风湿关节炎(病例)患者和 15870 名对照者的 129464 个标记物进行了分析。我们将这些数据与来自其他独立病例(n=2363)和对照者(n=17872)的 GWAS 数据进行了荟萃分析。我们确定了 14 个新的易感基因座,其中 9 个与类风湿关节炎总体相关,5 个与抗瓜氨酸肽抗体阳性的疾病相关,使在欧洲血统人群中确认的类风湿关节炎风险基因座数量达到 46 个。我们将 19 个基因座的关联峰细化到单个基因,在 6 个基因座上确定了次要的独立效应,并在 4 个基因座上确定了与低频变异体的关联。生物信息学分析为 7 个基因座的因果 SNP 生成了强有力的假说。本研究说明了密集 SNP 图谱分析在随后的功能研究中的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803c/3605761/397cc7b0366c/emss-50373-f0001.jpg

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