ArticleACR open rheumatology2026
Methotrexate Therapy in Juvenile Idiopathic Arthritis: No Clinically Relevant Pulmonary Impairment but Frequent Transient Liver Enzyme Elevations in a Longitudinal Single-Center Pediatric Cohort of 274 Children Over 30 Years.
Article in ACR open rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
- Erratum issued
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveMethotrexate (MTX) is a cornerstone in treating juvenile idiopathic arthritis (JIA). The long-term impact of MTX, particularly on pulmonary and liver function, remains a concern. We longitudinally examined the effects of MTX on pulmonary and hepatic function in the largest reported cohort to date.
methodsIn this retrospective, single-center study, patients with JIA receiving MTX (10-15 mg/m
resultsA total of 274 patients with JIA (189 female patients and 85 male patients) with a mean age at disease onset of 7.8 years were treated with MTX for a mean duration of 42.7 months (maximum 14.3 years), corresponding to 918 treatment-years. No clinically relevant MTX-associated lung disease occurred, and spirometric, lung volume, and diffusion parameters remained stable over time. One-third of the 274 pt hat RANSIENT liver enzyme elevations in liver enzyme levels that resolved after dose adjustment or temporary interruption; only 17 of 63 affected patients required permanent discontinuation due to recurrent transaminase elevations. No structural hepatic pathology was detected. Overall, MTX was discontinued in 59% of patients, most commonly due to sustained remission (53%). Other reasons included GPT elevation, nausea, cytopenia, inefficacy, and noncompliance and accounted for only a small minority of patients.
conclusionIn children with JIA, long-term treatment with MTX appears to be safe regarding the pulmonary outcome. Hepatic involvement was frequent but transient, occasionally requiring dose adjustment or discontinuation without long-term complications.
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