Aponte J, Petrelli M
Department of Medicine, Cleveland Metropolitan General Hospital, Case Western Reserve University, Ohio.
Arthritis Rheum. 1988 Dec;31(12):1457-64. doi: 10.1002/art.1780311201.
Twenty-three patients with severe rheumatoid arthritis were treated with oral methotrexate (MTX) for more than 10 years. MTX was given as a bolus of 5-15 mg/week; the total cumulative dose ranged from 4,690 mg to 10,230 mg. Liver biopsies were performed on 21 of the patients to assess possible fibrosis and cirrhosis. Grade I histopathologic changes were found in 13 of the 21 biopsy samples, grade II changes were found in 3, and grade IIIA changes (mild fibrosis) were found in 5 specimens. None of the biopsy samples showed cirrhosis. Repeat biopsies were performed on the 5 patients with grade IIIA changes while they were still taking MTX. No progression of the fibrosis was noted. Two of the 5 samples, however, were graded IIIB because of portal and perilobular inflammation. Our findings support the premise that prolonged administration of oral MTX, when given as a weekly bolus at a low dose, does not cause cirrhosis or severe fibrosis in the rheumatoid arthritis patient who does not abuse alcohol.
23例重症类风湿关节炎患者接受口服甲氨蝶呤(MTX)治疗超过10年。MTX以每周5 - 15mg的剂量推注给药;累积总剂量为4690mg至10230mg。对其中21例患者进行了肝脏活检以评估可能的纤维化和肝硬化情况。在21份活检样本中,13份发现有I级组织病理学改变,3份发现有II级改变,5份标本发现有IIIA级改变(轻度纤维化)。所有活检样本均未显示肝硬化。对5例有IIIA级改变的患者在仍服用MTX期间进行了重复活检。未发现纤维化进展。然而,5份样本中有2份因门脉和小叶周围炎症而被评为IIIB级。我们的研究结果支持这样一个前提,即对于不酗酒的类风湿关节炎患者,以低剂量每周推注的方式长期口服MTX不会导致肝硬化或严重纤维化。