Cui Chao, Gao Shuai, Shi Jingfei, Wang Kai
Department of Infectious Disease, Qilu Hospital of Shandong University Dezhou Hospital, Dezhou, China.
Department of Hepatology, Qilu Hospital of Shandong University, Jinan, China, 3Department of Clinical and Basic Medicine, Shandong First Medical University, Jinan, China.
Gut Liver. 2025 May 8. doi: 10.5009/gnl240539.
Metabolic dysfunction-associated steatotic liver disease (MASLD) has emerged as one of the most prevalent chronic liver diseases globally, and its pathogenesis is closely linked to the imbalance of intestinal microbiota and their metabolites. This article reviews the mechanisms through which intestinal microbiota influence the progression of MASLD via the gut-liver axis, elaborating on the complex roles of immune cell hyperactivation, impaired intestinal barrier function, and intestinal microbial metabolites such as short-chain fatty acids and bile acids. The imbalance of intestinal microbiota not only directly promotes the development of MASLD but also further exacerbates disease progression through abnormalities in their metabolites. Various novel therapeutic strategies are being actively developed on the basis of gut-liver axis theory, including probiotic/prebiotic/synbiotic treatment, fecal microbiota transplantation, and targeted drug therapy. These strategies aim to precisely regulate microbial homeostasis and improve glucose and lipid metabolism, thereby alleviating hepatic inflammation and fibrosis and optimizing the therapeutic outcomes of patients with MASLD. In the future, as research progresses, we will further uncover the interaction mechanisms between intestinal microbiota and MASLD and continuously explore more effective treatment methods, with the goal of improving the prognosis and quality of life for MASLD patients.
代谢功能障碍相关脂肪性肝病(MASLD)已成为全球最常见的慢性肝病之一,其发病机制与肠道微生物群及其代谢产物的失衡密切相关。本文综述了肠道微生物群通过肠-肝轴影响MASLD进展的机制,阐述了免疫细胞过度激活、肠道屏障功能受损以及短链脂肪酸和胆汁酸等肠道微生物代谢产物的复杂作用。肠道微生物群的失衡不仅直接促进MASLD的发展,还通过其代谢产物异常进一步加剧疾病进展。基于肠-肝轴理论,正在积极开发各种新型治疗策略,包括益生菌/益生元/合生元治疗、粪便微生物群移植和靶向药物治疗。这些策略旨在精确调节微生物稳态,改善糖脂代谢,从而减轻肝脏炎症和纤维化,优化MASLD患者的治疗效果。未来,随着研究的进展,我们将进一步揭示肠道微生物群与MASLD之间的相互作用机制,并不断探索更有效的治疗方法,以期改善MASLD患者的预后和生活质量。