• 1 January 1976
    • journal article
    • research article
    • Vol. 84 (3), 262-270
Abstract
Eighty-eight patients with severe, recalcitrant psoriasis had liver biopsies performed before and after methotrexate (MTX) therapy. MTX was given for an average of 26 mo. as a single, weekly, oral dose of 25 mg maximum. The mean cumulative dose was 1733 mg (range 175-4590 mg). A statistically significant increase in the number of pathological post-MTX liver biopsies was found (P < 0.0001). Of the 88 patients 6 developed cirrhosis and another 5 developed fibrosis, a total of 12.5%, during MTX therapy (95% confidence limits for cirrhosis: 3-14%). There was no statistically significant correlation between the number of pathological post-MTX liver biopsy findings in the 88 patients and the following variables: cumulative dose of MTX, duration of MTX therapy and admitted alcoholic intake during MTX therapy. Cirrhosis and fibrosis did not develop statistically more frequently from pathological than normal pre-MTX liver histology (P = 0.062). The liver damage appeared to be due to a multifactorial interaction of straining factors on the liver during MTX therapy. A multifactorial index comprising cumulative dose of MTX, admitted alcoholic intake during MTX therapy, age, obesity and, if available, pre-MTX liver histology gave an estimate of the probability of developing cirrhosis or fibrosis during treatment of psoriasis with weekly, oral doses of MTX. For use of MTX therapy in psoriasis the following precautions are suggested: MTX therapy should be used only in disabling cases, a pre-MTX liver biopsy and repeat liver biopsies at regular intervals of 1/2-1 yr should be performed, alcohol should be prohibited and frequent inquiries should be made about the patient''s alcoholic intake and strong reliance should not be placed on the SGOT [serum glutamic oxalacetic transaminase] as an indicator of abnormal liver histology.