Byrne Christopher D, Armandi Angelo, Pellegrinelli Vanessa, Vidal-Puig Antonio, Bugianesi Elisabetta
National Institute for Health and Care Research, Southampton Biomedical Research Centre, University Hospital Southampton and University of Southampton, Southampton, UK.
Division of Gastroenterology and Hepatology, Department of Medical Sciences, University of Turin, Turin, Italy.
Nat Rev Gastroenterol Hepatol. 2025 May;22(5):314-328. doi: 10.1038/s41575-025-01045-z. Epub 2025 Feb 17.
Μetabolic dysfunction-associated steatotic liver disease (MASLD) comprises a heterogeneous condition in the presence of steatotic liver. There can be a hierarchy of metabolic risk factors contributing to the severity of metabolic dysfunction and, thereby, the associated risk of both liver and extrahepatic outcomes, but the precise ranking and combination of metabolic syndrome (MetS) traits that convey the highest risk of major adverse liver outcomes and extrahepatic disease complications remains uncertain. Insulin resistance, low-grade inflammation, atherogenic dyslipidaemia and hypertension are key to the mechanisms of liver and extrahepatic complications. The liver is pivotal in MetS progression as it regulates lipoprotein metabolism and secretes substances that affect insulin sensitivity and inflammation. MASLD affects the kidneys, heart and the vascular system, contributing to hypertension and oxidative stress. To address the global health burden of MASLD, intensified by obesity and type 2 diabetes mellitus epidemics, a holistic, multidisciplinary approach is essential. This approach should focus on both liver disease management and cardiometabolic risk factors. This Review examines the link between metabolic dysfunction and liver dysfunction and extrahepatic disease outcomes, the diverse mechanisms in MASLD due to metabolic dysfunction, and a comprehensive, personalized management model for patients with MASLD.
代谢功能障碍相关脂肪性肝病(MASLD)是一种在存在脂肪性肝病情况下的异质性疾病。导致代谢功能障碍严重程度进而影响肝脏及肝外结局相关风险的代谢危险因素可能存在层级关系,但对于传达主要不良肝脏结局和肝外疾病并发症最高风险的代谢综合征(MetS)特征的确切排序和组合仍不确定。胰岛素抵抗、低度炎症、致动脉粥样硬化性血脂异常和高血压是肝脏及肝外并发症机制的关键因素。肝脏在MetS进展中起关键作用,因为它调节脂蛋白代谢并分泌影响胰岛素敏感性和炎症的物质。MASLD会影响肾脏、心脏和血管系统,导致高血压和氧化应激。为应对因肥胖和2型糖尿病流行而加剧的MASLD全球健康负担,采用整体、多学科方法至关重要。这种方法应同时关注肝脏疾病管理和心脏代谢危险因素。本综述探讨了代谢功能障碍与肝功能障碍及肝外疾病结局之间的联系、代谢功能障碍导致MASLD的多种机制,以及针对MASLD患者的全面、个性化管理模式。