Open AccessAutoinflammatory genes and susceptibility to psoriatic juvenile idiopathic arthritis
Author(s) -
Day T. G.,
Ramanan A. V.,
Hinks A.,
Lamb R.,
Packham J.,
Wise C.,
Punaro M.,
Donn R. P.
Publication year - 2008
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.23604
Subject(s) - mefv , single nucleotide polymorphism , psoriatic arthritis , medicine , snp , bonferroni correction , genotype , genotyping , arthritis , genetic association , genetics , gene , biology , gene mutation , mutation , statistics , mathematics
Objective To investigate the association of NLRP3, NOD2, MEFV, and PSTPIP1 , genes that cause 4 of the autoinflammatory hereditary periodic fever syndromes (HPFS), with juvenile idiopathic arthritis (JIA). Methods Fifty‐one single‐nucleotide polymorphisms (SNPs) across the 4 loci were investigated using MassArray genotyping in 950 Caucasian patients with JIA living in the UK and 728 ethnically matched healthy controls. Results Prior to Bonferroni correction for multiple testing, significant genotype associations between 6 SNPs in MEFV and JIA were observed and, in subgroup analysis, associations between 12 SNPs across all 4 loci and the subgroup of patients with psoriatic JIA were found. After Bonferroni correction for multiple testing, 2 genotype associations remained significant in the subgroup of patients with psoriatic JIA ( MEFV SNP rs224204 [corrected P = 0.025] and NLRP3 SNP rs3806265 [corrected P = 0.04]). Conclusion These findings support the use of monogenic loci as candidates for investigating the genetic component of complex disease and provide preliminary evidence of association between SNPs in autoinflammatory genes and psoriatic JIA. Our findings raise the interesting possibility of a shared disease mechanism between the HPFS and psoriatic JIA, potentially involving abnormal production of interleukin‐1β.