Shu Jian-Zhong, Huang Yu-Han, He Xiao-Hong, Liu Feng-Ying, Liang Qian-Qian, Yong Xue-Tong, Xie Yong-Fang
Department of Encephalopathy, Chongqing Hospital of Traditional Chinese Medicine, Chongqing 400015, China.
School of Life Health Information Science and Engineering, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.
World J Hepatol. 2025 Mar 27;17(3):103854. doi: 10.4254/wjh.v17.i3.103854.
In the current era, metabolic dysfunction-associated steatotic liver disease (MASLD) has gradually developed into a major type of chronic liver disease that is widespread globally. Numerous studies have shown that the gut microbiota plays a crucial and indispensable role in the progression of MASLD. Currently, the gut microbiota has become one of the important entry points for the research of this disease. Therefore, the aim of this review is to elaborate on the further associations between the gut microbiota and MASLD, including the changes and differences in the microbiota between the healthy liver and the diseased liver. Meanwhile, considering that metabolic dysfunction-associated fatty liver and metabolic dysfunction-associated steatohepatitis are abnormal pathological states in the development of the disease and that the liver exhibits different degrees of fibrosis (such as mild fibrosis and severe fibrosis) during the disease progression, we also conduct a comparison of the microbiota in these states and use them as markers of disease progression. It reveals the changes in the production and action mechanisms of short-chain fatty acids and bile acids brought about by changes in the gut microbiota, and the impact of lipopolysaccharide from Gram-negative bacteria on the disease. In addition, the regulation of the gut microbiota in disease and the production and inhibition of related disease factors by the use of probiotics (including new-generation probiotics) will be explored, which will help to monitor the disease progression of patients with different gut microbiota compositions in the future and carry out personalized targeted therapies for the gut microbiota. This will achieve important progress in preventing and combating this disease.
在当前时代,代谢功能障碍相关脂肪性肝病(MASLD)已逐渐发展成为全球范围内广泛存在的主要慢性肝病类型。众多研究表明,肠道微生物群在MASLD的进展中起着至关重要且不可或缺的作用。目前,肠道微生物群已成为该疾病研究的重要切入点之一。因此,本综述的目的是详细阐述肠道微生物群与MASLD之间的进一步关联,包括健康肝脏与患病肝脏之间微生物群的变化和差异。同时,鉴于代谢功能障碍相关脂肪性肝病和代谢功能障碍相关脂肪性肝炎是该疾病发展过程中的异常病理状态,且肝脏在疾病进展过程中表现出不同程度的纤维化(如轻度纤维化和重度纤维化),我们还对这些状态下的微生物群进行了比较,并将其用作疾病进展的标志物。它揭示了肠道微生物群变化所带来的短链脂肪酸和胆汁酸产生及作用机制的改变,以及革兰氏阴性菌的脂多糖对该疾病的影响。此外,还将探讨肠道微生物群在疾病中的调节作用以及使用益生菌(包括新一代益生菌)对相关疾病因子的产生和抑制作用,这将有助于未来监测不同肠道微生物群组成患者的疾病进展,并针对肠道微生物群进行个性化靶向治疗。这将在预防和对抗该疾病方面取得重要进展。