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Methotrexate hepatotoxicity in patients with rheumatoid arthritis
R Sotoudehmanesh1, B Anvari1, M Akhlaghi1
1Digestive Disease Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Abstract:
BACKGROUND Increases in aminotransferases (transaminitis) are potential major adverse reactions seen with long-term use of methotrexate (MTX). The aim of this study, therefore was to evaluate the incidence of MTX induced hepatotoxicity and its risk factors among rheumatoid arthritis (RA) patients. METHODS This retrospective study described 286 patients with RA who received ≥ 7.5 mg MTX weekly in an academic rheumatology clinic over a 15 year period. The results of serial liver function tests, concurrent MTX dose, cumulative dose and use of hepatotoxic drugs were collected and statistically analyzed according to a consecutive elevation in aminotransferases which occurred over at least a two week interval. RESULTS During the study period, 286 patients (84.4% female) with mean age of 46.6±12.7 years (18-84 years) were enrolled. Transaminitis occurred among 23.7% of patients (incidence: 6.9 per 100 person-years) during 40.5±34.6 month's exposure to MTX (989.6 person-years). The time difference between onset of therapy and occurrence of transaminitis was 22.1±22.0 months. The only significant factor related to the occurrence of transaminitis was the duration of MTX therapy. The average duration of treatment among patients with transaminitis (59.6±42.3 months) was greater than those with no transaminitis (p<0.001). The cumulative dose of MTX was significantly related to the occurrence of transaminitis (p<0.001). CONCLUSION MTX hepatotoxicity is a common complication of long-term treatment with MTX. It is associated with mild liver enzyme elevation and related to the duration of therapy.
Insights
Methotrexate (MTX) can cause liver damage (hepatotoxicity) in rheumatoid arthritis patients, particularly with long-term use. Duration of therapy and cumulative dose are key risk factors for elevated liver enzymes.
Area of Science:
- Rheumatology
- Hepatology
- Clinical Pharmacology
Background:
- Long-term methotrexate (MTX) use in rheumatoid arthritis (RA) is associated with potential aminotransferase elevations (transaminitis).
- Understanding the incidence and risk factors for MTX-induced hepatotoxicity is crucial for patient management.
Purpose of the Study:
- To evaluate the incidence of methotrexate-induced hepatotoxicity in rheumatoid arthritis patients.
- To identify risk factors associated with MTX-induced liver enzyme elevations.
Main Methods:
- Retrospective study of 286 RA patients treated with MTX (≥ 7.5 mg/week) over 15 years.
- Analysis of serial liver function tests, MTX dose (concurrent and cumulative), and concurrent hepatotoxic drug use.
- Statistical analysis focused on consecutive aminotransferase elevations over at least two weeks.
Main Results:
- Transaminitis occurred in 23.7% of patients (6.9 per 100 person-years) after a mean MTX exposure of 40.5 months.
- Significant risk factors for transaminitis included longer duration of MTX therapy (59.6 months vs. no transaminitis) and higher cumulative MTX dose.
- The average time to transaminitis onset was 22.1 months.
Conclusions:
- Methotrexate hepatotoxicity is a common complication in long-term RA treatment.
- Elevated liver enzymes are typically mild and directly related to the duration of MTX therapy and cumulative dose.
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