Busting the myth of methotrexate chronic hepatotoxicity.
Vincent Di MartinoDelphine Weil VerhoevenFrank VerhoevenFrançois AubinJerome AvouacLucine VuittonFrédéric LiotéThierry ThevenotDaniel WendlingPublished in: Nature reviews. Rheumatology (2022)
Methotrexate is a key component of the treatment of inflammatory rheumatic diseases and the mainstay of therapy in rheumatoid arthritis. Hepatotoxicity has long been a concern for prescribers envisaging long-term treatment with methotrexate for their patients. However, the putative liver toxicity of methotrexate should be evaluated in the context of advances in our knowledge of the pathogenesis and natural history of liver disease, especially non-alcoholic fatty liver disease (NAFLD). Notably, patients with NAFLD are at increased risk for methotrexate hepatotoxicity, and methotrexate can worsen the course of NAFLD. Understanding the mechanisms of acute hepatotoxicity can facilitate the interpretation of elevated concentrations of liver enzymes in this context. Liver fibrosis and the mechanisms of fibrogenesis also need to be considered in relation to chronic exposure to methotrexate. A number of non-invasive tests for liver fibrosis are available for use in patients with rheumatic disease, in addition to liver biopsy, which can be appropriate for particular individuals. On the basis of the available evidence, practical suggestions for pretreatment screening and long-term monitoring of methotrexate therapy can be made for patients who have (or are at risk for) chronic liver disease.
Keyphrases
- liver fibrosis
- high dose
- drug induced
- end stage renal disease
- rheumatoid arthritis
- ejection fraction
- newly diagnosed
- chronic kidney disease
- peritoneal dialysis
- oxidative stress
- prognostic factors
- stem cells
- patient reported outcomes
- mesenchymal stem cells
- bone marrow
- hepatitis b virus
- intensive care unit
- disease activity
- acute respiratory distress syndrome
- cell therapy
- aortic dissection