Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients

BACKGROUND: Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic condition of childhood. Genetic association studies have revealed several JIA susceptibility loci with the strongest effect size observed in the human leukocyte antigen (HLA) region. Genome-wide association studies have augmented the number of JIA-associated loci, particularly for non-HLA genes. The aim of this study was to identify new associations at non-HLA loci predisposing to the risk of JIA development in Estonian patients. METHODS: We performed genome-wide association analyses in an entire JIA case–control sample (All-JIA) and in a case–control sample for oligoarticular JIA, the most prevalent JIA subtype. The entire cohort was genotyped using the Illumina HumanOmniExpress BeadChip arrays. After imputation, 16,583,468 variants were analyzed in 263 cases and 6956 controls. RESULTS: We demonstrated nominal evidence of association for 12 novel non-HLA loci not previously implicated in JIA predisposition. We replicated known JIA associations in CLEC16A and VCTN1 regions in the oligoarticular JIA sample. The strongest associations in the All-JIA analysis were identified at PRKG1 (P = 2,54 × 10(−6)), LTBP1 (P = 9,45 × 10(−6)), and ELMO1 (P = 1,05 × 10(−5)). In the oligoarticular JIA analysis, the strongest associations were identified at NFIA (P = 5,05 × 10(−6)), LTBP1 (P = 9,95 × 10(−6)), MX1 (P = 1,65 × 10(−5)), and CD200R1 (P = 2,59 × 10(−5)). CONCLUSION: This study increases the number of known JIA risk loci and provides additional evidence for the existence of overlapping genetic risk loci between JIA and other autoimmune diseases, particularly rheumatoid arthritis. The reported loci are involved in molecular pathways of immunological relevance and likely represent genomic regions that confer susceptibility to JIA in Estonian patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10067-021-05756-x.