表达数量性状基因座
单核苷酸多态性
医学
全基因组关联研究
类风湿性关节炎
数量性状位点
SNP公司
人类白细胞抗原
遗传关联
基因
遗传学
免疫学
生物
基因型
抗原
作者
Katriona Goldmann,Athina Spiliopoulou,Andrii Iakovliev,Darren Plant,Nisha Nair,Cankut Çubuk,Paul McKeigue,Michael R. Barnes,Anne Barton,Costantino Pitzalis,Myles Lewis
标识
DOI:10.1136/ard-2023-224540
摘要
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.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.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 HLA-DPB2 with the critical triad of single-nucleotide polymorphisms (SNPs) rs3128921 driving synovial HLA-DPB2 expression, and both rs3128921 and HLA-DPB2 gene expression correlating with clinical severity and increasing probability of the lympho-myeloid pathotype.This analysis highlights the need to explore functional consequences of genetic associations in disease tissue. HLA-DPB2 SNP rs3128921 could potentially be used to stratify patients to more aggressive treatment immediately at diagnosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI