Department of Cardiology, National University Heart Centre, National University Hospital, Singapore, Singapore.
Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Semin Liver Dis. 2022 Aug;42(3):379-400. doi: 10.1055/a-1877-9656. Epub 2022 Jun 16.
Nonalcoholic steatohepatitis (NASH) is a burgeoning global health crisis that mirrors the obesity pandemic. This global health crisis has stimulated active research to develop novel NASH pharmacotherapies targeting dysregulated inflammatory, cellular stress, and fibrogenetic processes that include (1) metabolic pathways to improve insulin sensitivity, de novo lipogenesis, and mitochondrial utilization of fatty acids; (2) cellular injury or inflammatory targets that reduce inflammatory cell recruitment and signaling; (3) liver-gut axis targets that influence bile acid enterohepatic circulation and signaling; and (4) antifibrotic targets. In this review, we summarize several of the therapeutic agents that have been studied in phase 2 and 3 randomized trials. In addition to reviewing novel therapeutic drugs targeting nuclear receptor pathways, liver chemokine receptors, liver lipid metabolism, lipotoxicity or cell death, and glucagon-like peptide-1 receptors, we also discuss the rationale behind the use of combination therapy and the lessons learned from unsuccessful or negative clinical trials.
非酒精性脂肪性肝炎(NASH)是一场正在迅速蔓延的全球健康危机,与肥胖症大流行如出一辙。这场全球健康危机刺激了人们积极开展研究,以开发针对失调的炎症、细胞应激和纤维发生过程的新型 NASH 药物疗法,其中包括:(1) 改善胰岛素敏感性、从头合成脂肪和脂肪酸线粒体利用的代谢途径;(2) 减少炎症细胞募集和信号转导的细胞损伤或炎症靶点;(3) 影响胆汁酸肠肝循环和信号转导的肝肠轴靶点;以及 (4) 抗纤维化靶点。在这篇综述中,我们总结了一些已在 2 期和 3 期随机临床试验中研究过的治疗药物。除了审查针对核受体途径、肝趋化因子受体、肝脂质代谢、脂毒性或细胞死亡以及胰高血糖素样肽-1 受体的新型治疗药物外,我们还讨论了联合治疗的应用原理以及从不成功或负面临床试验中吸取的教训。