Hashkes P J, Balistreri W F, Bove K E, Ballard E T, Passo M H
Department of Pediatrics, Rebecca Sieff and Poriah Hospitals, Safed and Tiberias, Israel.
J Pediatr. 1999 Jan;134(1):47-52. doi: 10.1016/s0022-3476(99)70371-9.
To examine the relationship between hepatotoxic risk factors and liver histopathology in patients with juvenile rheumatoid arthritis (JRA) treated with methotrexate (MTX).
We graded the histology of 33 percutaneous liver biopsy specimens from 25 patients with JRA treated at Children's Hospital Medical Center, Cincinnati, Ohio, using the Roenigk Classification Scale. Stepwise linear and logistic regression analyses were performed to examine the relationship of the Roenigk grade and presence of liver fibrosis of biopsy specimens with potential risk factors.
Twenty-seven biopsy specimens (82%) were classified as grade I, 4 (12%) as grade II, and 2 (6%) as grade IIIA; none demonstrated significant fibrosis. The frequency of biochemical abnormalities (P <.001) and body mass index (P =.05) were the only risk factors found to significantly relate to the Roenigk grade. The following factors were not significantly associated with the Roenigk grade: age, gender, disease duration, JRA subtype and course, duration of MTX administration, weekly MTX dose, cumulative dose of MTX, route of MTX administration, use of folic acid supplementation, concurrent use of other medications, and potential hepatotoxic comorbidities.
Serial biochemical abnormalities are significantly associated with Roenigk grade and the presence of liver fibrosis. These findings concur with studies of patients with rheumatoid arthritis, suggesting that guidelines for monitoring MTX hepatotoxicity in rheumatoid arthritis may be applicable to patients with JRA.
探讨接受甲氨蝶呤(MTX)治疗的幼年类风湿关节炎(JRA)患者肝毒性危险因素与肝脏组织病理学之间的关系。
我们使用罗宁克分类量表对俄亥俄州辛辛那提儿童医院医疗中心收治的25例JRA患者的33份经皮肝活检标本的组织学进行分级。进行逐步线性和逻辑回归分析,以检验活检标本的罗宁克分级和肝纤维化与潜在危险因素之间的关系。
27份活检标本(82%)被分类为I级,4份(12%)为II级,2份(6%)为IIIA级;均未显示明显纤维化。生化异常频率(P<.001)和体重指数(P =.05)是仅有的与罗宁克分级显著相关的危险因素。以下因素与罗宁克分级无显著关联:年龄、性别、病程、JRA亚型和病程、MTX给药持续时间、每周MTX剂量、MTX累积剂量、MTX给药途径、叶酸补充剂的使用、其他药物的同时使用以及潜在的肝毒性合并症。
连续生化异常与罗宁克分级及肝纤维化显著相关。这些发现与类风湿关节炎患者的研究结果一致,提示类风湿关节炎中监测MTX肝毒性的指南可能适用于JRA患者。