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托伐普坦在常染色体显性多囊肾病中的安全性;聚焦于特异质性药物性肝损伤风险。

Tolvaptan safety in autosomal-dominant polycystic kidney disease; a focus on idiosyncratic drug-induced liver injury liabilities.

作者信息

Hammond Sean, Meng Xiaoli, Barber Jane, Mosedale Merrie, Chadwick Amy, Watkins Paul B, Naisbitt Dean J

机构信息

Department of Pharmacology and Therapeutics, Centre for Drug Safety Science, University of Liverpool, Liverpool, L69 3GE, United Kingdom.

ApconiX, Alderley Edge, SK10 4TG, United Kingdom.

出版信息

Toxicol Sci. 2025 Jan 1;203(1):11-27. doi: 10.1093/toxsci/kfae142.

Abstract

Tolvaptan is a vasopressin V2 receptor antagonist which has proven to be an effective and mostly well-tolerated agent for the treatment of autosomal-dominant polycystic kidney disease. However, its administration is associated with rare but serious idiosyncratic liver injury, which has warranted a black box warning on the drug labels and frequent monitoring of liver blood tests in the clinic. This review outlines mechanistic investigations that have been conducted to date and constructs a working narrative as an explanation for the idiosyncratic drug-induced liver injury (IDILI) events that have occurred thus far. Potential risk factors which may contribute to individual susceptibility to DILI reactions are addressed, and key areas for future investigative/clinical development are highlighted.

摘要

托伐普坦是一种血管加压素V2受体拮抗剂,已被证明是治疗常染色体显性多囊肾病的一种有效且大多耐受性良好的药物。然而,其使用与罕见但严重的特异质性肝损伤有关,这使得药物标签上有黑框警告,并且在临床中需要频繁监测肝脏血液检查。本综述概述了迄今为止所进行的机制研究,并构建了一个可行的叙述,以解释迄今为止发生的特异质性药物性肝损伤(IDILI)事件。文中探讨了可能导致个体对药物性肝损伤反应易感性的潜在风险因素,并突出了未来研究/临床开发的关键领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10f9/11664107/4085bb14f886/kfae142f1.jpg

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