Miyake Yasuhiro, Iwasaki Yoshiaki, Terada Ryo, Takagi Shinjiro, Okamaoto Ryoichi, Ikeda Hiroshi, Sakai Nobuyuki, Makino Yasuhiro, Kobashi Haruhiko, Takaguchi Kouichi, Sakaguchi Kohsaku, Shiratori Yasushi
Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine and Dentistry, 2-5-1, Shikata-cho, Okayama 700-8558, Japan.
J Hepatol. 2005 Dec;43(6):951-7. doi: 10.1016/j.jhep.2005.06.006. Epub 2005 Jul 7.
BACKGROUND/AIMS: Autoimmune hepatitis shows a good response to immunosuppressive treatment, and the prognosis may be determined by the clinical course. The present study was conducted in order to analyze the factors contributing to the outcomes of patients with type 1 autoimmune hepatitis.
Eighty-four consecutive patients with type 1 autoimmune hepatitis were followed up regularly for a median follow-up period of 70.5 months (16.2-163 months). We analyzed the prognostic factors using time-fixed and time-dependent Cox proportional hazard models. The end point was progression of the disease to decompensated liver cirrhosis.
Seventy-seven patients (92%) were treated with prednisolone during the follow-up period, and 11 patients (13%) developed decompensated liver cirrhosis. Using a time-dependent multivariate model, the starting dose of corticosteroid (dose of prednisolone <20 mg/day), relapse within 3 months after the normalization of serum alanine aminotransferase levels with initial treatment, and elevated serum alanine aminotransferase levels during the follow-up period (>40 IU/L), all showed a significant association with progression of the disease.
The prognosis of type 1 autoimmune hepatitis on adequate immunosuppressive treatment improves when the serum alanine aminotransferase level persists at < or = 40 IU/L. Factors existing prior to medical treatment may not affect the prognosis.
背景/目的:自身免疫性肝炎对免疫抑制治疗反应良好,其预后可能由临床病程决定。本研究旨在分析影响1型自身免疫性肝炎患者预后的因素。
对84例连续的1型自身免疫性肝炎患者进行定期随访,中位随访期为70.5个月(16.2 - 163个月)。我们使用时间固定和时间依赖的Cox比例风险模型分析预后因素。终点为疾病进展至失代偿期肝硬化。
77例患者(92%)在随访期间接受了泼尼松龙治疗,11例患者(13%)发展为失代偿期肝硬化。使用时间依赖多变量模型,皮质类固醇起始剂量(泼尼松龙剂量<20mg/天)、初始治疗血清丙氨酸氨基转移酶水平正常化后3个月内复发以及随访期间血清丙氨酸氨基转移酶水平升高(>40IU/L)均与疾病进展显著相关。
当血清丙氨酸氨基转移酶水平持续≤40IU/L时,1型自身免疫性肝炎在充分免疫抑制治疗下的预后改善。治疗前存在的因素可能不影响预后。