新型酒精性肝病干预措施。
Novel intervention for alcohol-associated liver disease.
机构信息
Department of Endocrinology, The Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou 310003, Zhejiang Province, China.
Laboratory Medicine Center, Department of Clinical Laboratory, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou 310014, Zhejiang Province, China.
出版信息
World J Gastroenterol. 2024 Oct 21;30(39):4308-4312. doi: 10.3748/wjg.v30.i39.4308.
A recently published article in the clarified that elafibranor, a dual peroxisome proliferator activated receptor α/δ (PPARα/δ) agonist, reduced inflammation and fibrosis in alcohol-associated liver disease (ALD). This letter aims to discuss the findings presented in that article. ALD is a global health problem, and no effective drugs has been approved by the Food and Drug Administration to cure it. Thus, finding targeted therapies is of great urgency. Herein, we focus on the pathogenesis of ALD and the role of PPARα/δ in its development. Consistent with the conclusion of the article of interest, we think that elafibranor may be a promising therapeutic option for ALD, due to the pivotal involvement of PPARα/δ in the pathogenesis of the disease. However, its treatment dose, timing, and side effects need to be further investigated in future studies.
最近发表在《》的一篇文章阐明,双过氧化物酶体增殖物激活受体α/δ(PPARα/δ)激动剂 Elafibranor 可减轻酒精性肝病(ALD)中的炎症和纤维化。本函旨在讨论该文章中提出的研究结果。ALD 是一个全球性的健康问题,美国食品和药物管理局尚未批准任何有效的药物来治愈它。因此,寻找有针对性的治疗方法迫在眉睫。在此,我们重点介绍 ALD 的发病机制以及 PPARα/δ 在其发病过程中的作用。与感兴趣的文章的结论一致,我们认为 Elafibranor 可能是治疗 ALD 的一种有前途的治疗选择,因为 PPARα/δ 在该疾病的发病机制中起着关键作用。然而,其治疗剂量、时间和副作用需要在未来的研究中进一步探讨。