Department of Internal Medicine, MedStar Georgetown University Hospital, Washington, DC, USA.
Department of Gastroenterology, MedStar Georgetown University Hospital, Washington, DC, USA.
Expert Rev Gastroenterol Hepatol. 2022 Aug;16(8):767-785. doi: 10.1080/17474124.2022.2101996. Epub 2022 Jul 22.
In 2021, over 3,000 articles on Drug-Induced Liver Injury (DILI) were published, nearly doubling the annual number compared to 2011. This review selected DILI articles from 2021 we felt held the greatest interest and clinical relevance.
A literature search was conducted using PubMed between 1 March 2021 and 28 February 2022. 86 articles were included. This review discusses new and established cases of hepatotoxins, including new FDA approvals and COVID-19 therapeutics. Developments in biomarkers and causality assessment methods are discussed. Updates from registries are also explored.
DILI diagnosis and prognostication remain challenging. Roussel Uclaf Causality Assessment Method (RUCAM) is the best option for determining causality and has been increasingly accepted by clinicians. Revised Electronic Causality Assessment Method (RECAM) may be more user-friendly and accurate but requires further validation. Quantitative systems pharmacology methods, such as DILIsym, are increasingly used to predict hepatotoxicity. Oncotherapeutic agents represent many newly approved and described causes of DILI. Such hepatotoxicity is deemed acceptable relative to the benefit these drugs offer. Drugs developed for non-life-threatening disorders may not show a favorable benefit-to-risk ratio and will be more difficult to approve. As the COVID-19 landscape evolves, its effect on DILI deserves further investigation.
2021 年,发表了超过 3000 篇关于药物性肝损伤(DILI)的文章,与 2011 年相比,几乎翻了一番。本篇综述选择了我们认为最具兴趣和临床相关性的 2021 年 DILI 文章。
使用 PubMed 进行了文献检索,检索时间为 2021 年 3 月 1 日至 2022 年 2 月 28 日。共纳入 86 篇文章。本文讨论了新的和已确立的肝毒素病例,包括新的 FDA 批准和 COVID-19 治疗方法。讨论了生物标志物和因果关系评估方法的发展。还探讨了来自登记处的更新。
DILI 的诊断和预后仍然具有挑战性。Roussel Uclaf 因果关系评估方法(RUCAM)是确定因果关系的最佳选择,已越来越被临床医生所接受。修订后的电子因果关系评估方法(RECAM)可能更易用且准确,但需要进一步验证。定量系统药理学方法,如 DILIsym,越来越多地用于预测肝毒性。肿瘤治疗剂代表了许多新批准和描述的 DILI 原因。与这些药物带来的益处相比,这种肝毒性被认为是可以接受的。为非危及生命的疾病开发的药物可能不会显示出有利的获益-风险比,因此更难获得批准。随着 COVID-19 形势的发展,其对 DILI 的影响值得进一步研究。