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类风湿关节炎表达数量性状基因座分析确定与严重程度和结局相关的组织特异性变异。

Expression quantitative trait loci analysis in rheumatoid arthritis identifies tissue specific variants associated with severity and outcome.

机构信息

Centre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Queen Mary University of London, London, UK.

Centre for Population Health Sciences, Usher Institute, University of Edinburgh, Edinburgh, UK.

出版信息

Ann Rheum Dis. 2024 Feb 15;83(3):288-299. doi: 10.1136/ard-2023-224540.

DOI:10.1136/ard-2023-224540
PMID:37979960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10894812/
Abstract

OBJECTIVE

Genome-wide association studies have successfully identified more than 100 loci associated with susceptibility to rheumatoid arthritis (RA). However, our understanding of the functional effects of genetic variants in causing RA and their effects on disease severity and response to treatment remains limited.

METHODS

In this study, we conducted expression quantitative trait locus (eQTL) analysis to dissect the link between genetic variants and gene expression comparing the disease tissue against blood using RNA-Sequencing of synovial biopsies (n=85) and blood samples (n=51) from treatment-naïve patients with RA from the Pathobiology of Early Arthritis Cohort.

RESULTS

This identified 898 eQTL genes in synovium and genes loci in blood, with 232 genes in common to both synovium and blood, although notably many eQTL were tissue specific. Examining the HLA region, we uncovered a specific eQTL at with the critical triad of single-nucleotide polymorphisms (SNPs) rs3128921 driving synovial expression, and both rs3128921 and gene expression correlating with clinical severity and increasing probability of the lympho-myeloid pathotype.

CONCLUSIONS

This analysis highlights the need to explore functional consequences of genetic associations in disease tissue. SNP rs3128921 could potentially be used to stratify patients to more aggressive treatment immediately at diagnosis.

摘要

目的

全基因组关联研究已成功鉴定出 100 多个与类风湿关节炎(RA)易感性相关的位点。然而,我们对遗传变异导致 RA 的功能效应及其对疾病严重程度和治疗反应的影响的理解仍然有限。

方法

在这项研究中,我们进行了表达数量性状基因座(eQTL)分析,以剖析遗传变异与基因表达之间的联系,比较了来自未经治疗的 RA 患者的滑膜活检(n=85)和血液样本(n=51)的疾病组织与血液,使用 RNA 测序。

结果

这在滑膜中鉴定出了 898 个 eQTL 基因和血液中的基因座,其中 232 个基因在滑膜和血液中都有,尽管许多 eQTL 是组织特异性的。在检查 HLA 区域时,我们在 发现了一个特定的 eQTL,其中关键的三核苷酸多态性(SNP)rs3128921 驱动滑膜中的 表达,rs3128921 和 基因表达与临床严重程度和淋巴髓样表型的概率增加相关。

结论

这项分析强调了需要在疾病组织中探索遗传关联的功能后果。SNP rs3128921 可用于在诊断时立即对患者进行更积极的治疗分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b51/10894812/989d81ec80d2/ard-2023-224540f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b51/10894812/989d81ec80d2/ard-2023-224540f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b51/10894812/989d81ec80d2/ard-2023-224540f01.jpg

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