Liu Hanyang, Lefere Sander, Guillot Adrien, Zheng Ming-Hua, Tacke Frank
Department of Hepatology and Gastroenterology, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum and Campus Charité Mitte, Berlin, Germany.
Cell Biology and Imaging Section, Thoracic and GI Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Hepatology. 2025 May 30. doi: 10.1097/HEP.0000000000001417.
Metabolic dysfunction-associated steatotic liver diseases (MASLDs) encompass a spectrum of liver disorders primarily defined by hepatic steatosis and cardiometabolic risk factors. MASLD affects over 30% of the global adult population, representing a substantial risk for public health. MASLD can progress from simple steatosis to steatohepatitis (termed MASH), marked by inflammation and fibrosis, potentially leading to cirrhosis and liver cancer. Obesity has been identified as one of the leading risk factors for MASLD, fueling the concept that efficient anti-obesity therapy will halt MASLD progression. Bariatric surgery (also termed metabolic and bariatric surgery, MBS) has become a well-established intervention for class III obesity and class II obesity with comorbidities, offering significant and sustained weight loss. The common MBS procedures (eg, Roux-en-Y gastric bypass and sleeve gastrectomy) were indeed found to improve MASLD by ameliorating hepatic steatosis, inflammation, fibrosis, and reducing cancer risk in patients with MASLD/MASH. These effects may go beyond a simple consequence of restricted dietary intake, as illustrated by a growing body of studies showing MBS-induced transcriptional program changes in the liver. Given the mounting evidence from preclinical research, clinical trials, and advanced biotechnologies emerging in recent years, refined histological and cellular in-depth characterization in MBS-treated MASLD is anticipated. This review summarizes the current knowledge on the pathogenic and therapeutic effects of MBS on MASLD, with the hope of inspiring further mechanistic and translational studies.
代谢功能障碍相关脂肪性肝病(MASLD)涵盖一系列主要由肝脂肪变性和心脏代谢危险因素定义的肝脏疾病。MASLD影响全球超过30%的成年人口,对公共卫生构成重大风险。MASLD可从单纯性脂肪变性发展为脂肪性肝炎(称为MASH),其特征为炎症和纤维化,可能导致肝硬化和肝癌。肥胖已被确定为MASLD的主要危险因素之一,这强化了高效抗肥胖治疗将阻止MASLD进展的观念。减重手术(也称为代谢和减重手术,MBS)已成为治疗III级肥胖和伴有合并症的II级肥胖的成熟干预措施,可实现显著且持续的体重减轻。常见的MBS手术(如Roux-en-Y胃旁路术和袖状胃切除术)确实被发现可通过改善肝脂肪变性、炎症、纤维化以及降低MASLD/MASH患者的癌症风险来改善MASLD。这些作用可能不仅仅是饮食摄入受限的简单结果,越来越多的研究表明MBS可诱导肝脏转录程序改变就说明了这一点。鉴于近年来临床前研究、临床试验和先进生物技术提供越来越多的证据,预计对接受MBS治疗的MASLD进行更精细的组织学和细胞深度表征。本综述总结了目前关于MBS对MASLD的致病和治疗作用的知识,希望能激发进一步的机制和转化研究。