Recovery from liraglutide-induced acute liver injury assessed for causality using the updated RUCAM as global gold standard: A case report and literature review.

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Fenli Su, WeiChi Lu
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引用次数: 0

Abstract

Liraglutide is a glucagon-like peptide-1 receptor agonist (GLP-1RA) widely used for managing type 2 diabetes mellitus (T2DM) and obesity. Reports of liraglutide-associated hepatotoxicity are exceedingly rare. To our knowledge, this is the 9th case of drug-induced liver injury (DILI) caused by liraglutide to be reported. We present a case of a 40-year-old Chinese woman who developed acute liver injury with elevated liver enzymes following 2 weeks of liraglutide treatment for T2DM. Causality was assessed using the updated RUCAM scale, yielding a score of 7, indicating probable DILI, and the diagnosis was further confirmed by liver biopsy. Liver enzyme levels normalized after discontinuing the drug and administering liver-protective treatment within 3 weeks. Furthermore, this case report includes a comprehensive review of all published cases of liraglutide-associated DILI, emphasizing the necessity of regular hepatic-biochemistry monitoring in patients receiving GLP-1 receptor agonists such as liraglutide and providing meaningful evidence regarding their hepatotoxic risk.

使用更新的RUCAM作为全球金标准评估利拉鲁肽诱导的急性肝损伤恢复的因果关系:一份病例报告和文献回顾。
利拉鲁肽是一种胰高血糖素样肽-1受体激动剂(GLP-1RA),广泛用于治疗2型糖尿病(T2DM)和肥胖。利拉鲁肽相关肝毒性的报道极为罕见。据我们所知,这是第9例利拉鲁肽引起的药物性肝损伤(DILI)的报道。我们报告了一例40岁的中国女性,她在接受利拉鲁肽治疗2周后出现急性肝损伤,肝酶升高。使用更新的RUCAM量表评估因果关系,得分为7分,表明可能存在DILI,并通过肝活检进一步证实诊断。停药并给予保肝治疗后3周内肝酶水平恢复正常。此外,本病例报告包括对所有已发表的利拉鲁肽相关DILI病例的全面回顾,强调对接受GLP-1受体激动剂(如利拉鲁肽)治疗的患者进行定期肝生化监测的必要性,并提供有关其肝毒性风险的有意义的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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