TY - JOUR T1 - Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms JF - Annals of the Rheumatic Diseases JO - Ann Rheum Dis SP - 321 LP - 328 DO - 10.1136/annrheumdis-2020-218481 VL - 80 IS - 3 AU - Elena López-Isac AU - Samantha L Smith AU - Miranda C Marion AU - Abigail Wood AU - Marc Sudman AU - Annie Yarwood AU - Chenfu Shi AU - Vasanthi Priyadarshini Gaddi AU - Paul Martin AU - Sampath Prahalad AU - Stephen Eyre AU - Gisela Orozco AU - Andrew P Morris AU - Carl D Langefeld AU - Susan D Thompson AU - Wendy Thomson AU - John Bowes Y1 - 2021/03/01 UR - http://ard.bmj.com/content/80/3/321.abstract N2 - Objectives Juvenile idiopathic arthritis (JIA) is the most prevalent form of juvenile rheumatic disease. Our understanding of the genetic risk factors for this disease is limited due to low disease prevalence and extensive clinical heterogeneity. The objective of this research is to identify novel JIA susceptibility variants and link these variants to target genes, which is essential to facilitate the translation of genetic discoveries to clinical benefit.Methods We performed a genome-wide association study (GWAS) in 3305 patients and 9196 healthy controls, and used a Bayesian model selection approach to systematically investigate specificity and sharing of associated loci across JIA clinical subtypes. Suggestive signals were followed-up for meta-analysis with a previous GWAS (2751 cases/15 886 controls). We tested for enrichment of association signals in a broad range of functional annotations, and integrated statistical fine-mapping and experimental data to identify target genes.Results Our analysis provides evidence to support joint analysis of all JIA subtypes with the identification of five novel significant loci. Fine-mapping nominated causal single nucleotide polymorphisms with posterior inclusion probabilities ≥50% in five JIA loci. Enrichment analysis identified RELA and EBF1 as key transcription factors contributing to disease risk. Our integrative approach provided compelling evidence to prioritise target genes at six loci, highlighting mechanistic insights for the disease biology and IL6ST as a potential drug target.Conclusions In a large JIA GWAS, we identify five novel risk loci and describe potential function of JIA association signals that will be informative for future experimental works and therapeutic strategies. ER -