Ciardullo Stefano, Muraca Emanuele, Vergani Michela, Invernizzi Pietro, Perseghin Gianluca
Department of Medicine and Rehabilitation, Policlinico di Monza, Monza, Italy.
Department of Medicine and Surgery, University of Milano Bicocca, Milan, Italy.
Gastroenterol Rep (Oxf). 2024 Apr 26;12:goae029. doi: 10.1093/gastro/goae029. eCollection 2024.
In the present narrative review, we have summarized evidence on the pharmacological treatment of non-alcoholic fatty liver disease (NAFLD)/metabolic dysfunction-associated steatotic liver disease (MASLD). We start by reviewing the epidemiology of the condition and its close association with obesity and type 2 diabetes. We then discuss how randomized-controlled trials are performed following guidance from regulatory agencies, including differences and similarities between requirements of the US Food and Drug Administration and the European Medicine Agency. Difficulties and hurdles related to limitations of liver biopsy, a large number of screening failures in recruiting patients, as well as unpredictable response rates in the placebo group are evaluated. Finally, we recapitulate the strategies employed for potential drug treatments of this orphan condition. The first is to repurpose drugs that originally targeted T2DM and/or obesity, such as pioglitazone, glucagon-like peptide 1 receptor agonists (liraglutide and semaglutide), multi-agonists (tirzepatide and retatrutide), and sodium-glucose transporter 2 inhibitors. The second is to develop drugs specifically targeting NAFLD/MASLD. Among those, we focused on resmetirom, fibroblast growth factor 21 analogs, and lanifibranor, as they are currently in Phase 3 of their clinical trial development. While many failures have characterized the field of pharmacological treatment of NAFLD/MASLD in the past, it is likely that approval of the first treatments is near. As occurs in many chronic conditions, combination therapy might lead to better outcomes. In the case of non-alcoholic steatohepatitis, we speculate that drugs treating underlying metabolic co-morbidities might play a bigger role in the earlier stages of disease, while liver-targeting molecules will become vital in patients with more advanced disease in terms of inflammation and fibrosis.
在本叙述性综述中,我们总结了关于非酒精性脂肪性肝病(NAFLD)/代谢功能障碍相关脂肪性肝病(MASLD)药物治疗的证据。我们首先回顾该疾病的流行病学及其与肥胖和2型糖尿病的密切关联。然后,我们讨论如何根据监管机构的指导进行随机对照试验,包括美国食品药品监督管理局和欧洲药品管理局要求之间的异同。评估了与肝活检局限性、招募患者时大量筛选失败以及安慰剂组不可预测的反应率相关的困难和障碍。最后,我们概括了针对这种罕见病潜在药物治疗所采用的策略。第一种是重新利用最初针对2型糖尿病和/或肥胖的药物,如吡格列酮、胰高血糖素样肽1受体激动剂(利拉鲁肽和司美格鲁肽)、多靶点激动剂(替尔泊肽和雷特鲁肽)以及钠-葡萄糖协同转运蛋白2抑制剂。第二种是开发专门针对NAFLD/MASLD的药物。其中,我们重点关注瑞美替昂、成纤维细胞生长因子21类似物和拉尼非诺,因为它们目前正处于临床试验开发的3期阶段。虽然过去NAFLD/MASLD药物治疗领域有许多失败案例,但首批治疗药物的获批可能已为期不远。正如在许多慢性病中一样,联合治疗可能会带来更好的结果。对于非酒精性脂肪性肝炎,我们推测治疗潜在代谢合并症的药物可能在疾病早期发挥更大作用,而在炎症和纤维化更严重的疾病阶段,靶向肝脏的分子将变得至关重要。