Systemic juvenile idiopathic arthritis: are there any predictors of disease course?

Clicks: 1
ID: 320613
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal

Ranked #137 of 197 articles by views in Lara D. Veeken

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 197 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Abstract Background Systemic juvenile idiopathic arthritis (sJIA) is an autoinflammatory disorder with a variable disease course presenting either as monophasic or non-monophasic (polycyclic or persistent) course. Identifying clinical and laboratory features at presentation predicting these trajectories may guide early therapeutic decisions. This study aimed to evaluate predictors of disease course in children. Methods We conducted a retrospective observational study of children with sJIA over 18 years. Clinical features, laboratory parameters, treatment and disease outcomes were reviewed. Children with sJIA were classified as having monophasic, polycyclic or persistent disease based on clinical course. Logistic regression analysis, adjusted for age, gender, year of diagnosis, was performed to evaluate predictors of non-monophasic disease. Results Eighty children with sJIA were included, median age at diagnosis was 8 years (IQR 3.5-11) with median follow-up of 6 years (IQR 3-10). 34 (42.5%) monophasic, 8 (10%) polycyclic, and 38(47.5%) had persistent course. Rash (83.8%) followed by arthritis (66.3%) were most common presenting features, while macrophage activation syndrome (MAS) occurred in 18.8%. Polyarthritis at presentation was independently associated with non-monophasic disease (OR 12.68, 95% CI 2.69-59.90, p = 0.001). There was weak evidence to support an association between the clinical features and laboratory parameters, including MAS at presentation and disease trajectory. Conclusion sJIA is heterogenous and difficult to predict disease course at initial presentation. Polyarthritis identified children at high risk of a non-monophasic disease course in this study population. Early identification of these high-risk children may support timely escalation of targeted biologic therapy and improved long-term outcomes.
Reference Key
openalex_W7168050160 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Ashwini Prithvi, Chaitra Govardhan, Bushra Aladaileh, Florence Z. Martin, Athimalaipet V Ramanan
Journal Lara D. Veeken
Year 2026
DOI
10.1093/rheumatology/keag366
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.