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Methotrexate therapy may prevent the onset of uveitis in juvenile idiopathic arthritis
Charalampia Papadopoulou1, Mikhail Kostik, Marek Böhm
1Istituto Giannina Gaslini, Genova, Italy.
Insights
Early methotrexate (MTX) treatment may prevent uveitis in children with juvenile idiopathic arthritis. Further randomized controlled trials are needed to confirm MTX
Area of Science:
- Pediatric Rheumatology
- Ophthalmology
Background:
- Juvenile idiopathic arthritis (JIA) is a common cause of pediatric uveitis.
- Uveitis in JIA can lead to significant vision loss if not managed promptly.
Purpose of the Study:
- To determine if early methotrexate (MTX) treatment can prevent the onset of uveitis in pediatric patients with JIA.
- To analyze the incidence of uveitis in JIA patients treated with and without MTX.
Main Methods:
- Retrospective review of clinical charts for 254 JIA patients with disease duration under 1 year.
- Patients received stable management for 2 years with or without MTX; exclusions applied for other systemic medications or specific JIA subtypes.
- Uveitis onset was monitored over a 2-year follow-up period.
Main Results:
- Of 254 patients, 86 received MTX and 168 did not. Uveitis developed in 16.9% of patients overall.
- The incidence of uveitis was significantly lower in the MTX-treated group (10.5%) compared to the untreated group (20.2%) (P = .049).
- Survival analysis indicated a reduced probability of developing uveitis with early MTX treatment.
Conclusions:
- Early MTX therapy shows potential in preventing uveitis in children with JIA.
- Confounding by indication necessitates further investigation via randomized controlled trials to confirm MTX's efficacy in reducing ocular disease incidence.
Objective:
To evaluate whether early treatment with methotrexate (MTX) prevents the onset of uveitis in children with juvenile idiopathic arthritis.
Study Design:
The clinical charts of all consecutive patients seen between January 2002 and February 2011 who had a disease duration <1 year at first visit and had received a stable management for at least 2 years with or without MTX were reviewed. Patients who were given systemic medications other than MTX (except nonsteroidal anti-inflammatory drugs) were excluded. Patients with systemic arthritis, rheumatoid factor-positive arthritis, or enthesitis-related arthritis were also excluded. In each patient, the 2-year follow-up period after first visit was examined to establish whether uveitis had occurred.
Results:
A total of 254 patients with a median disease duration of 0.3 year were included. Eighty-six patients (33.9%) were treated with MTX, whereas 168 patients (66.1%) did not receive MTX. During the 2-year follow-up, 211 patients (83.1%) did not develop uveitis, whereas 43 patients (16.9%) had uveitis a median of 1.0 year after the first visit. The frequency of uveitis was lower in MTX-treated than in MTX-untreated patients (10.5% vs 20.2%, respectively, P = .049). Survival analysis confirmed that patients treated with MTX had a lower probability of developing uveitis.
Conclusion:
Early MTX therapy may prevent the onset of uveitis in children with juvenile idiopathic arthritis. Because our study may be affected by confounding by indication, the potential of MTX to reduce the incidence of ocular disease should be investigated in a randomized controlled trial.
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