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Juvenile Psoriatic Arthritis (JPsA): juvenile arthritis with psoriasis?
Yonatan Butbul Aviel1, Pascal Tyrrell, Rayfel Schneider
1Division of Rheumatology, SickKids Hospital, Hospital for Sick Children Research Institute, University of Toronto, Toronto, ON, Canada. earl.silverman@sickkids.ca.
Insights
Juvenile psoriatic arthritis (JPsA) generally has a good long-term outcome. Patients with JPsA do not form distinct subgroups but resemble other juvenile idiopathic arthritis (JIA) subtypes without psoriasis.
Area of Science:
- Pediatric Rheumatology
- Inflammatory Arthritis
- Childhood Rheumatic Diseases
Background:
- Juvenile psoriatic arthritis (JPsA) is an increasingly recognized inflammatory arthritis in children.
- Limited data exists on the long-term characteristics and outcomes of JPsA compared to other juvenile idiopathic arthritis (JIA) subtypes.
Purpose of the Study:
- To investigate the long-term outcomes and clinical course of pediatric patients diagnosed with JPsA.
- To identify potential distinct subgroups within the JPsA patient population.
Main Methods:
- Retrospective review of clinical records for 119 patients meeting JPsA criteria.
- Classification into four groups based on clinical features and onset type.
- Analysis of patient characteristics, clinical features at onset, and during follow-up.
Main Results:
- The cohort included oligoarticular-onset (55%), polyarticular (33%), and enthesitis-related arthritis (ERA) (13%) JPsA.
- ERA patients were older and more frequently male at diagnosis.
- Nail and distal interphalangeal (DIP) joint involvement were common, particularly in polyarticular JPsA.
Conclusions:
- The long-term prognosis for JPsA is generally favorable.
- JPsA patients do not appear to represent a unique subgroup but rather share characteristics with JIA subtypes lacking psoriasis.
Background:
Following the introduction of the ILAR criteria for juvenile idiopathic arthritis, juvenile psoriatic arthritis (JPsA) has become a better recognized category within the inflammatory arthritides of childhood. There are fewer reports describing the characteristics and long-term outcome of patients with JPsA than other subtypes of JIA.The aim of our study was to determine the long-term outcome and clinical course of patients with juvenile psoriatic arthritis (JPsA) and to define subgroups of JPsA.
Methods:
Clinical records of all patients meeting criteria for JPsA were reviewed and divided into 4 groups depending on their clinical features and onset type. Patient characteristics and clinical features at onset and during follow-up were determined.
Results:
The cohort consisted of 119 patients: 65 with oligoarticular-onset (55%; persistent 44 and extended 21), 34 (29%) with RF(-) and 4 (3%) RF(+) polyarticular and 16 (13%) enthesitis-related arthritis (ERA). At diagnosis patients with ERA were oldest and more commonly male (p=0.001 and =0.01 respectively). Patients with a polyarticular course had more involvement of small joints of the hands and wrist when compared to patients with persistent oligoarticular and ERA (p<0.001) while patients with ERA had more hip and sacroiliac arthritis (p<0.001 for both). Nail changes were seen in 66 patients (57%) and were associated with DIP involvement (p=0.0034).
Outcome:
Time to first inactive disease on, but not off, therapy was significantly longer among patients with polyarticular course when compared to oligoarticular and ERA (p=0.016 and p=0.48 respectively). Patients with polyarticular course more frequently had contractures during follow-up than other groups (p=0.01).
Conclusion:
The long-term outcome of with JPsA was generally good. Patients with JPsA did not appear to form distinct sub-group of patients but rather resembled JIA patients with onset types without psoriasis.
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