PT - JOURNAL ARTICLE AU - YONATAN AVIEL BUTBUL AU - PASCAL N. TYRRELL AU - RAYFEL SCHNEIDER AU - SANDEEP DHILLON AU - BRIAN M. FELDMAN AU - RONALD M. LAXER AU - ROTRAUD K. SAURENMANN AU - LYNN SPIEGEL AU - BONNIE CAMERON AU - SHIRLEY M. TSE AU - EARL D. SILVERMAN TI - Comparison of Patients with Juvenile Psoriatic Arthritis and Nonpsoriatic Juvenile Idiopathic Arthritis: How Different Are They? AID - 10.3899/jrheum.080674 DP - 2009 Sep 01 TA - The Journal of Rheumatology PG - 2033--2041 VI - 36 IP - 9 4099 - http://www.jrheum.org/content/36/9/2033.short 4100 - http://www.jrheum.org/content/36/9/2033.full SO - J Rheumatol2009 Sep 01; 36 AB - Objective. To compare the clinical features and outcome between patients with juvenile psoriatic arthritis (JPsA) and non-JPsA juvenile idiopathic arthritis (JIA). Methods. Fifty-three children with JPsA, 32 with < 5 joints in the first 6 months of disease (oligo–JPsA) and 21 (≥ 5 joints) polyarticular-onset (poly-JPsA) were compared to 53 patients with JIA who were matched by sex, age, date of diagnosis, and articular onset pattern. Results. There was no difference in the percentage of patients between the oligoarticular groups who developed extended oligoarthritis or in the percentage of patients who were positive for antinuclear antibodies. The only differences were that 25% of patients with oligo-JPsA had dactylitis compared to 0% of patients with oligo-JIA (p < 0.01) and 50% had nail pitting as compared to 18.7% (p < 0.05). In polyarticular patients the percentages with dactylitis were similar (19% vs 38%; p = 0.25). The frequency of uveitis was identical in the oligoarticular patients but a higher rate was seen in poly-JPsA compared to poly-JIA (23.8% vs 0%; p = 0.02), while contractures were more frequent in poly-JIA compared to poly-JPsA during the course of the illness (47.6% vs 14.3%; p = 0.03) but not at last followup (14.3% vs 4.7%; p = 0.6). At last followup the mean Childhood Health Assessment Questionnaire scores were similar in both the polyarticular and oligoarticular groups. Conclusion. There were only a few differences between patients with JPsA and JIA regarding disease onset, disease course, and outcome. We suggest that large, longterm prospective studies are required to accurately determine whether subdividing JIA according to psoriasis is worthwhile.