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Lung function in children and adolescents with juvenile idiopathic arthritis during long-term treatment with
Christoph Leiskau1, Angelika Thon, Monika Gappa
1Division of Pediatric Pneumology, Allergology and Neonatology, Dept. of Pediatrics, Hannover Medical School, Hannover, Germany. christoph-leiskau@gmx.de
Objectives:
Methotrexate may cause severe adverse pulmonary side-effects in adults with rheumatoid arthritis. Our aim was to examine the long-term effect of MTX on lung function in patients with juvenile idiopathic arthritis (JIA).
Methods:
We retrospectively reviewed the charts of all 68 patients with JIA treated with MTX at our centre over a 14-year period. Results of annual pulmonary function tests (PFT) were compared using paired t-tests adjusted by Bonferroni correction and by linear regression analysis.
Results:
The patients in our study had taken MTX for a median of 6.7 years with a median cumulative dose of 3219 mg. In a subgroup of 37 patients PFT had been performed before the onset of MTX. In this subgroup there was a significant decrease of mean mid-expiratory flow (MMEF) after 3 years (-14.0%, p<0.001) of MTX. Diffusion capacity of the lung for carbon monoxide (DLCO) was reduced after the third year (-12.4%, p=0.001). In the total group there was a decrease in MMEF between years 3 and 4 after MTX onset (-13.5%, p=0.001). Forced expiratory volume (FEV1) showed a slight rise between years 4 and 5 (+5.5%, p=0.003). All other parameters remained without significant changes. There was no correlation of PFT results and cumulative MTX dose or JIA subtype. None of our patients developed clinically relevant lung disease.
Conclusions:
In summary we found some declines of MMEF and DLCO during long-term treatment with MTX. Overall our data confirm the relative safety of long-term MTX treatment in patients with JIA. We conclude that further data on the development of pulmonary function in patients receiving MTX therapy would be helpful.
Insights
Long-term methotrexate (MTX) treatment in juvenile idiopathic arthritis (JIA) patients showed some decline in lung function, specifically MMEF and DLCO. However, overall safety was confirmed, with no clinically significant lung disease observed.
Area of Science:
- Pediatric Rheumatology
- Pulmonary Medicine
- Pharmacology
Background:
- Methotrexate (MTX) is associated with pulmonary adverse events in adults with rheumatoid arthritis.
- Long-term effects of MTX on lung function in juvenile idiopathic arthritis (JIA) require further investigation.
Purpose of the Study:
- To evaluate the long-term impact of MTX on pulmonary function tests (PFTs) in patients diagnosed with JIA.
- To assess the safety profile of MTX concerning respiratory health in a pediatric population.
Main Methods:
- Retrospective chart review of 68 JIA patients treated with MTX over 14 years.
- Analysis of annual PFT results using paired t-tests and linear regression.
- Comparison of PFTs before MTX initiation and at various time points during treatment.
Main Results:
- A subgroup of 37 patients showed significant decreases in mean mid-expiratory flow (MMEF) by -14.0% and diffusion capacity (DLCO) by -12.4% after 3 years of MTX.
- The total group exhibited a -13.5% decrease in MMEF between years 3 and 4.
- Forced expiratory volume (FEV1) slightly increased (+5.5%) between years 4 and 5; no correlation found between PFT changes, cumulative MTX dose, or JIA subtype. No patients developed clinically significant lung disease.
Conclusions:
- Long-term MTX treatment in JIA patients may lead to modest declines in MMEF and DLCO.
- The study supports the relative safety of long-term MTX therapy in JIA patients regarding pulmonary function.
- Further research is recommended to monitor pulmonary function development in patients undergoing MTX therapy.
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