Combination therapies for metabolic dysfunction-associated steatohepatitis: challenges and opportunities

医学 胰岛素抵抗 耐受性 脂肪性肝炎 背景(考古学) 生物信息学 联合疗法 脂肪肝 药理学 不利影响 纤维化 FGF21型 2型糖尿病 代谢综合征 肝病 临床试验 胰岛素
作者
Xiao-Dong Zhou,Qi Fan,C Byrne,Giovanni Targher,Mark Muthiah,Daniel Q Huang,Qin-Fen Chen,Mazen Noureddin,Wenhao Li,Vlad Ratziu,Rohit Loomba,S. Francque,Arun J Sanyal,MING-HUA ZHENG
出处
期刊:Gut [BMJ]
卷期号:75 (4): 815-825 被引量:15
标识
DOI:10.1136/gutjnl-2025-337431
摘要

Metabolic dysfunction-associated steatohepatitis (MASH) is a multifactorial metabolic liver disease that occurs in the context of obesity, insulin resistance and cardiometabolic comorbidities. Monotherapy targeting single pathways often provides only partial improvements in histological liver fibrosis and systemic metabolic parameters, prompting growing interest in multitargeted combination therapies. Multitargeted and combination strategies for MASH can modulate multiple and complementary pathogenic processes, potentially improving efficacy, promoting liver fibrosis regression, optimising systemic metabolic outcomes and reducing treatment-related adverse effects. Liver-directed combination therapies, such as thyroid hormone receptor-beta (THR-β) agonists along with acetyl-CoA carboxylase (ACC) inhibitors or peroxisome proliferator-activated receptor agonists, aim to improve histological features of MASH. Regimens combining systemic metabolic and liver-specific agents, such as glucagon-like peptide-1 (GLP-1) receptor agonists with fibroblast growth factor-21 analogues or THR-β agonists, aim to optimise metabolic outcomes, including body weight, insulin resistance and plasma lipids. Thoughtfully designed drug pairings, such as diacylglycerol O-acyltransferase 2 inhibitors combined with ACC inhibitors or GLP-1 and glucagon receptor dual agonists, could improve safety and tolerability by leveraging complementary mechanisms that may mitigate adverse effects. These therapeutic strategies aim to achieve more comprehensive and durable improvements in both liver pathology and systemic health than single-agent therapy alone. This review integrates current knowledge on multitargeted and combination therapies for MASH, examines mechanistic rationales and emerging clinical evidence and addresses practical considerations for patient-centred implementation. Therefore, we aim to provide clinicians and researchers with a comprehensive framework to optimise individualised management and improve both hepatic and systemic outcomes in individuals living with MASH.
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