Thiele D L, DuCharme L, Cunningham M R, Mimms L T, Cuthbert J A, Lee W M, Combes B
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, USA.
Am J Gastroenterol. 1996 Feb;91(2):300-8.
The goals of this study were to examine responses to corticosteroid-containing therapy in non-B chronic hepatitis patients with different anti-hepatitis C virus (HCV), autoantibody, and biochemical test results and to determine what factors correlate with response.
Patients with a prior or current history of steroid therapy for putative autoimmune or chronic non-A, non-B hepatitis were assessed. Responses during the first 6 months of therapy were categorized as "complete" (normal aminotransferases for > or = 1 month), "partial" ( > 50% reduction), or "no response."
Sufficient data available to permit evaluation in 32 patients. Complete responses were noted in 17, partial responses in 12, and no response in three subjects. By multivariate analysis, only absence of anti-HCV and presence of cirrhosis were independent predictors of response. Nonresponders were found to have lower scores in a proposed autoimmune hepatitis scoring system, but scores of complete and partial responders were not significantly different. Despite a lower likelihood of a complete response, 80% (12/15) of patients with multiantigen positive anti-HCV tests had either partial or complete initial responses to corticosteroid-containing therapy, and, in nine patients, aminotransferases fell to < 2 times the upper limit of normal. All 15 anti-HCV-negative patients, but only three of 15 anti-HCV-positive patients, entered complete responses that were sustained (aminotransferases < twofold abnormal) on regimens containing < 20 mg/day or prednisolone or prednisone.
Although anti-HCV-positive patients frequently exhibit partial initial responses to immunosuppressive therapy, the absence of specific anti-HCV antibodies was better as a predictor of completeness of response than assessment of autoantibodies or degree of biochemical abnormalities.
本研究的目的是检查不同抗丙型肝炎病毒(HCV)、自身抗体和生化检测结果的非B型慢性肝炎患者对含皮质类固醇疗法的反应,并确定哪些因素与反应相关。
对曾接受或正在接受类固醇疗法治疗疑似自身免疫性或慢性非甲非乙型肝炎的患者进行评估。将治疗前6个月的反应分为“完全”(转氨酶正常≥1个月)、“部分”(降低>50%)或“无反应”。
有足够数据可供评估的患者有32例。17例有完全反应,12例有部分反应,3例无反应。通过多变量分析,只有抗HCV阴性和肝硬化是反应的独立预测因素。在拟议的自身免疫性肝炎评分系统中,无反应者得分较低,但完全反应者和部分反应者的得分无显著差异。尽管完全反应的可能性较低,但抗HCV检测多抗原阳性的患者中有80%(12/15)对含皮质类固醇疗法有部分或完全的初始反应,且有9例患者的转氨酶降至正常上限的<2倍。所有15例抗HCV阴性患者,但15例抗HCV阳性患者中只有3例,在接受<20mg/天泼尼松龙或泼尼松的方案治疗时进入完全反应且反应持续(转氨酶<正常上限的两倍)。
尽管抗HCV阳性患者对免疫抑制疗法经常表现出部分初始反应,但与评估自身抗体或生化异常程度相比,缺乏特异性抗HCV抗体更能预测反应的完全性。