Disease activity trajectories from childhood to adulthood in the population-based Nordic juvenile idiopathic arthritis cohort
View abstract on PubMed
Summary
This summary is machine-generated.Four long-term juvenile idiopathic arthritis (JIA) disease activity trajectories were identified. Patient
Area Of Science
- Pediatric Rheumatology
- Longitudinal Disease Trajectory Analysis
- Juvenile Idiopathic Arthritis (JIA)
Background
- Juvenile idiopathic arthritis (JIA) requires understanding long-term disease activity.
- The clinical Juvenile Arthritis Disease Activity Score (cJADAS10) is a key metric.
- Identifying distinct disease trajectories is crucial for patient management.
Purpose Of The Study
- To identify long-term disease activity trajectories in JIA patients from childhood to adulthood.
- To evaluate the contribution of cJADAS10 components to disease activity.
- To explore factors associated with active disease at 18-year follow-up.
Main Methods
- Utilized a population-based Nordic JIA cohort with 18-year follow-up.
- Employed discrete mixture models for longitudinal clustering of cJADAS10 and its components.
- Assessed patient's global assessment of well-being (PaGA) using hierarchical clustering and correlation analysis.
Main Results
- Identified four distinct cJADAS10-based disease activity trajectories in 427 JIA patients.
- Observed significant increases in PaGA and physician's global assessment (PhGA) in one trajectory group, without increased joint counts.
- Higher PaGA scores correlated with unfavorable patient-reported outcomes, indicating its significant impact.
Conclusions
- Identified distinct long-term disease activity trajectories in JIA.
- Patient's global assessment (PaGA) emerged as the primary driver of disease activity into adulthood.
- Emphasized the need for strategies to achieve patient- and physician-perceived inactive disease.
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