Kaplowitz Neil
Gastroenterology/Liver Division, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Clin Infect Dis. 2004 Mar 1;38 Suppl 2:S44-8. doi: 10.1086/381446.
Drug-induced hepatotoxicity is a frequent cause of liver injury. The predominant clinical presentation is acute hepatitis and/or cholestasis, although almost any clinical pathological pattern of acute or chronic liver disease can occur. The pathogenesis of drug-induced liver disease usually involves the participation of the parent drug or metabolites that either directly affect the cell biochemistry or elicit an immune response. Each hepatotoxin is associated with a characteristic signature regarding the pattern of injury and latency. However, some drugs may exhibit >1 signature. Susceptibility to drug-induced hepatotoxicity is also influenced by genetic and environmental risk factors. Unpredictable, low-frequency, idiosyncratic reactions often occur on a background of a higher rate of mild asymptomatic liver injury and, although difficult to predict, they may be detected by monitoring serum alanine aminotransferase levels. Recent and future advances in toxicogenomics and proteomics should improve the identification of risk factors and the understanding of idiosyncratic hepatotoxicity.
药物性肝毒性是肝损伤的常见原因。主要临床表现为急性肝炎和/或胆汁淤积,尽管几乎任何急性或慢性肝病的临床病理模式都可能出现。药物性肝病的发病机制通常涉及母体药物或代谢产物的参与,它们要么直接影响细胞生物化学,要么引发免疫反应。每种肝毒素都与损伤模式和潜伏期的特征性标志相关。然而,一些药物可能表现出>1种标志。药物性肝毒性的易感性也受遗传和环境风险因素影响。不可预测的、低频的特异质性反应通常发生在轻度无症状肝损伤发生率较高的背景下,虽然难以预测,但可通过监测血清丙氨酸转氨酶水平来检测。毒理基因组学和蛋白质组学的最新及未来进展应能改进风险因素的识别并增进对特异质性肝毒性的理解。