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Liver biopsy in methotrexate-treated psoriatics-a re-evalution
Acta Dermato-Venereologica
|January 1, 1975
Summary
Methotrexate treatment for psoriasis can lead to liver damage, including fatty infiltration and fibrosis. Regular liver biopsies are crucial for monitoring patients on long-term methotrexate therapy due to potential early signs of damage.
Area of Science:
- Hepatology
- Dermatology
- Pharmacology
Background:
- Methotrexate is a common treatment for psoriasis.
- Long-term methotrexate use is associated with potential liver toxicity.
- Monitoring liver health in psoriatic patients undergoing methotrexate therapy is essential.
Purpose of the Study:
- To evaluate the effects of methotrexate on liver biopsies in psoriatic patients.
- To identify risk factors associated with methotrexate-induced liver damage.
- To determine the necessity of liver biopsies for monitoring psoriatic patients on methotrexate.
Main Methods:
- Performed 286 liver biopsies in 139 psoriatic patients.
- Conducted pre- and post-methotrexate biopsies in 56 patients.
- Analyzed biopsy data for signs of fatty infiltration, fibrosis, and cirrhosis.
- Correlated liver damage with methotrexate dosage, alcohol consumption, and potassium arsenite use.
Main Results:
- A statistically significant increase in fatty infiltration was observed post-methotrexate treatment.
- Alcohol consumption was significantly associated with liver fibrosis.
- Potassium arsenite use showed a potential association with liver fibrosis.
- Three cases of liver cirrhosis appeared in patients with pre-existing fibrosis, despite intermittent methotrexate dosage.
Conclusions:
- Long-term methotrexate therapy in psoriatic patients can cause liver damage, including fatty infiltration and fibrosis.
- Early detection of liver damage is possible through liver biopsies, even with minor laboratory abnormalities.
- Regular liver biopsies are necessary for monitoring psoriatic patients on long-term methotrexate treatment.
- Disease severity may be a complicating factor in methotrexate-induced liver damage.