Liver Research Center, Beijing Friendship Hospital, Capital Medical University, National Clinical Research Center for Digestive Diseases, Beijing, China.
Department of Pathology, Yong Loo Lin School of Medicine, National University of Singapore, National University Hospital, Singapore, Singapore.
Mod Pathol. 2019 Dec;32(12):1795-1805. doi: 10.1038/s41379-019-0314-9. Epub 2019 Jul 12.
Histologically, drug-induced liver injury could be classified into acute hepatitis, chronic hepatitis, acute cholestasis, chronic cholestasis, and cholestatic hepatitis. The correlation between these histologic patterns and long-term clinical outcomes has not been well established. Therefore, we conducted a retrospective cohort study to investigate the association of histologic patterns and long-term clinical outcomes defined as biochemical normalization, persistent abnormal liver biochemistry or death at designated time points. In this study, biochemical classification was determined by R-values; histologic injury pattern was determined by morphological features. Predictive ability of clinical outcomes by these two classifications was assessed using Receiver Operating Characteristic Curves. Logistic regression was performed to identify histologic factors associated with outcomes. Totally, 88 patients with drug-induced liver injury were included for final analysis. Biochemical and histologic classification were consistent in 50 (57%) cases. 53 (60%) cases showed biochemical normalization within 6 months, and a further 11 (13%), 16 (18%), and 6 (7%) cases within 1, 2, and 3 years, respectively. Compared with biochemical classification, histologic injury pattern had better predictive ability for abnormal biochemistry at 6 months (Areas under Receiver Operating Characteristic Curves 0.92 versus 0.60, P < 0.001) and 1 year (Areas under Receiver Operating Characteristic Curves 0.94 versus 0.69, P < 0.001). Interlobular bile duct loss in >25% portal areas was independently associated with abnormal biochemistry at 6 months, 1 year, and 2 years. In conclusion, histologic injury pattern is better correlated with clinical outcome at 6 months and 1 year than biochemical classification. Moderate bile duct loss is an important histologic feature associated with persistent biochemical abnormality at 6 months, 1 year, and 2 years.
从组织学角度来看,药物性肝损伤可分为急性肝炎、慢性肝炎、急性胆汁淤积、慢性胆汁淤积和胆汁淤积性肝炎。这些组织学模式与长期临床结局之间的相关性尚未得到很好的确定。因此,我们进行了一项回顾性队列研究,以调查组织学模式与长期临床结局(定义为指定时间点的生化正常化、持续异常肝功能或死亡)之间的关系。在这项研究中,生化分类由 R 值确定;组织学损伤模式由形态特征确定。使用受试者工作特征曲线评估这两种分类对临床结局的预测能力。使用逻辑回归确定与结局相关的组织学因素。总共纳入 88 例药物性肝损伤患者进行最终分析。50 例(57%)患者的生化和组织学分类一致。53 例(60%)患者在 6 个月内生化正常化,进一步分别有 11 例(13%)、16 例(18%)和 6 例(7%)在 1、2 和 3 年内生化正常化。与生化分类相比,组织学损伤模式对 6 个月(受试者工作特征曲线下面积 0.92 对 0.60,P<0.001)和 1 年(受试者工作特征曲线下面积 0.94 对 0.69,P<0.001)异常肝功能具有更好的预测能力。>25%门管区的小叶间胆管缺失与 6 个月、1 年和 2 年的异常肝功能独立相关。总之,组织学损伤模式与 6 个月和 1 年的临床结局相关性优于生化分类。中度胆管缺失是与 6 个月、1 年和 2 年持续生化异常相关的重要组织学特征。