药物诱发的胆汁淤积性肝病。

IF 15.8 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Hepatology Pub Date : 2025-10-01 Epub Date: 2024-08-08 DOI:10.1097/HEP.0000000000001052
Einar S Bjornsson, Harshad C Devarbhavi
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引用次数: 0

摘要

对于出现以碱性磷酸酶(ALP)升高为主的肝脏化验指标升高的患者,胆汁淤积性药物引起的肝损伤是一个重要且经常具有挑战性的鉴别诊断。需要排除多种病因,如肝脏恶性肿瘤、胆总管结石、病毒性肝炎胆汁淤积症、败血症胆汁淤积症、原发性和继发性胆管炎以及右侧心力衰竭等。自 2011 年《肝脏病学》杂志发表上一篇关于药物性胆汁淤积的综述以来,人们对药物性胆汁淤积的临床表型、新病因、风险因素、病理生理学和遗传决定因素的理解和认识取得了重大进展。药物引起的继发性硬化性胆管炎(SSC)在几种不同的药物中都有详细的记录。检查点抑制剂(CPIs)是已证实可导致 SSC 的药物类型之一。最近,一些新的草药和膳食补充剂也被证明会导致胆汁淤积性肝损伤。在过去的十年中,人们发现了许多药物导致胆汁淤积的遗传风险因素,胆汁淤积性肝损伤背后的发病机制也得到了更好的界定。本综述的重点是诊断方法、新临床表型(如 SSC 和胆管消失综合征)的描述。此外,综述还概述了导致胆汁淤积的风险因素、遗传决定因素和肝胆转运体的病理生理学。还介绍了管理、不确定领域和未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug-induced cholestatic liver diseases.

Cholestatic DILI is an important and frequently challenging differential diagnosis in patients presenting with elevated liver tests with predominant elevation in alkaline phosphatase. A number of competing etiologies need to be ruled out, such as hepatobiliary malignancy, choledocholithiasis, cholestatic forms of viral hepatitis, cholestasis of sepsis, primary and secondary cholangitis, and right-sided cardiac failure to name a few. Important advances have occurred in the understanding and knowledge of the clinical phenotypes, new etiological agents, risk factors, pathophysiology, and genetic determinants of drug-induced cholestasis since the last review on drug-induced cholestasis was published in Hepatology in 2011. Secondary sclerosing cholangitis (SSC) due to drugs has been well documented for several different drugs. Checkpoint inhibitors are one of the types of drugs shown to lead to secondary sclerosing cholangitis. Several new herbal and dietary supplements have recently been shown to lead to cholestatic liver injury. A number of genetic risk factors for cholestasis due to drugs have been identified in the last decade, and the pathogenesis behind cholestatic injury is better defined. In this review, the focus is on diagnostic approach and description of new clinical phenotypes such as secondary sclerosing cholangitis and vanishing bile duct syndrome. Furthermore, the review provides an overview of the risk factors, genetic determinants, and the pathophysiology of hepatobiliary transporters leading to cholestasis. Management, areas of uncertainty, and future direction are also presented.

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来源期刊
Hepatology
Hepatology 医学-胃肠肝病学
CiteScore
27.50
自引率
3.70%
发文量
609
审稿时长
1 months
期刊介绍: HEPATOLOGY is recognized as the leading publication in the field of liver disease. It features original, peer-reviewed articles covering various aspects of liver structure, function, and disease. The journal's distinguished Editorial Board carefully selects the best articles each month, focusing on topics including immunology, chronic hepatitis, viral hepatitis, cirrhosis, genetic and metabolic liver diseases, liver cancer, and drug metabolism.
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