Tolman K G, Clegg D O, Lee R G, Ward J R
J Rheumatol Suppl. 1985 Dec;12 Suppl 12:29-34.
The findings of liver studies in 29 patients who were treated with low dose pulse methotrexate for rheumatoid arthritis (RA) are described. The biopsy specimens of 22 patients (76%) showed liver abnormalities, but cirrhosis did not develop in any patient. There were no statistically significant differences in age, duration of treatment, or cumulative dose between patients in whom abnormal liver histology developed and those in whom it did not. Our findings showed that isolated elevations of the aminotransferase enzymes or alkaline phosphatase levels did not predict liver disease, nor did the absence of elevation of these enzymes assure the absence of liver disease. Serial elevations of the aminotransferase and/or alkaline phosphatase enzyme levels and the development of hypoalbuminemia during treatment were specific indicators of the development of liver disease. In the patients studied, significant liver disease did not develop before 2 years of therapy or with a cumulative dose of methotrexate of less than 1500 mg.
本文描述了29例接受低剂量脉冲甲氨蝶呤治疗类风湿关节炎(RA)患者的肝脏研究结果。22例患者(76%)的活检标本显示肝脏异常,但无一例患者发展为肝硬化。肝脏组织学出现异常的患者与未出现异常的患者在年龄、治疗时间或累积剂量方面无统计学显著差异。我们的研究结果表明,单独的转氨酶或碱性磷酸酶水平升高并不能预测肝脏疾病,这些酶水平未升高也不能确保没有肝脏疾病。治疗期间转氨酶和/或碱性磷酸酶水平的持续升高以及低白蛋白血症的出现是肝脏疾病发展的特异性指标。在本研究的患者中,治疗2年之前或甲氨蝶呤累积剂量小于1500 mg时,未出现严重肝脏疾病。