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调查青少年特发性关节炎的类风湿关节炎易感基因座证实高度重叠。

Investigation of rheumatoid arthritis susceptibility loci in juvenile idiopathic arthritis confirms high degree of overlap.

机构信息

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

出版信息

Ann Rheum Dis. 2012 Jul;71(7):1117-21. doi: 10.1136/annrheumdis-2011-200814. Epub 2012 Jan 31.

Abstract

OBJECTIVES

Rheumatoid arthritis (RA) shares some similar clinical and pathological features with juvenile idiopathic arthritis (JIA); indeed, the strategy of investigating whether RA susceptibility loci also confer susceptibility to JIA has already proved highly successful in identifying novel JIA loci. A plethora of newly validated RA loci has been reported in the past year. Therefore, the aim of this study was to investigate these single nucleotide polymorphisms (SNP) to determine if they were also associated with JIA.

METHODS

Thirty-four SNP that showed validated association with RA and had not been investigated previously in the UK JIA cohort were genotyped in JIA cases (n=1242), healthy controls (n=4281), and data were extracted for approximately 5380 UK Caucasian controls from the Wellcome Trust Case-Control Consortium 2. Genotype and allele frequencies were compared between cases with JIA and controls using PLINK. A replication cohort of 813 JIA cases and 3058 controls from the USA was available for validation of any significant findings.

RESULTS

Thirteen SNP showed significant association (p<0.05) with JIA and for all but one the direction of association was the same as in RA. Of the eight loci that were tested, three showed significant association in the US cohort.

CONCLUSIONS

A novel JIA susceptibility locus was identified, CD247, which represents another JIA susceptibility gene whose protein product is important in T-cell activation and signalling. The authors have also confirmed association of the PTPN2 and IL2RA genes with JIA, both reaching genome-wide significance in the combined analysis.

摘要

目的

类风湿关节炎(RA)与幼年特发性关节炎(JIA)具有一些相似的临床和病理学特征;事实上,研究 RA 易感基因是否也会导致 JIA 易感性的策略已经在确定新的 JIA 基因座方面取得了巨大成功。过去一年中已经报道了大量新验证的 RA 基因座。因此,本研究旨在研究这些单核苷酸多态性(SNP),以确定它们是否也与 JIA 相关。

方法

在 JIA 病例(n=1242)、健康对照(n=4281)中对 34 个与 RA 有明确关联且之前未在英国 JIA 队列中进行研究的 SNP 进行基因分型,并从英国 Wellcome Trust 病例对照联盟 2 中提取了大约 5380 名英国白种人对照的数据。使用 PLINK 比较病例组与对照组之间的 JIA 基因型和等位基因频率。来自美国的 813 例 JIA 病例和 3058 例对照的复制队列可用于验证任何显著发现。

结果

13 个 SNP 与 JIA 显著相关(p<0.05),除一个外,所有 SNP 的关联方向与 RA 相同。在测试的 8 个基因座中,有 3 个在美国队列中显示出显著关联。

结论

确定了一个新的 JIA 易感基因座 CD247,这代表了另一个 JIA 易感基因,其蛋白质产物在 T 细胞激活和信号转导中很重要。作者还证实了 PTPN2 和 IL2RA 基因与 JIA 的关联,这两个基因在联合分析中均达到全基因组显著水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644a/3375583/634c31a0f45d/ard-71-7-1117-fig1.jpg

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