Wang Shendong, Yin Junhao, Liu Zhaojun, Liu Xin, Tian Ge, Xin Xijian, Qin Yiming, Feng Xiujing
Shandong Provincial Key Laboratory for Rheumatic Disease and Translational Medicine, The First Affiliated Hospital of Shandong First Medical University and Shandong Provincial Qianfoshan Hospital, Jinan, Shandong 250014, China; School of Clinical and Basic Medical Sciences, Shandong First Medical University& Shandong Academy of Medical Sciences, Jinan 250117, Shandong, China.
School of Life Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, Shandong 271000, China.
Life Sci. 2024 Dec 15;359:123211. doi: 10.1016/j.lfs.2024.123211. Epub 2024 Nov 2.
Metabolic dysfunction-associated steatotic liver disease (MASLD) represents a global health concern, affecting over 30 % of adults. It is a principal driver in the development of cirrhosis and hepatocellular carcinoma. The complex pathogenesis of MASLD involves an excessive accumulation of lipids, subsequently disrupting lipid metabolism and prompting inflammation within the liver. This review synthesizes the recent research progress in understanding the mechanisms contributing to MASLD progression, with particular emphasis on metabolic disorders and interorgan crosstalk. We highlight the molecular mechanisms linked to these factors and explore their potential as novel targets for pharmacological intervention. The insights gleaned from this article have important implications for both the prevention and therapeutic management of MASLD.
代谢功能障碍相关脂肪性肝病(MASLD)是一个全球性的健康问题,影响着超过30%的成年人。它是肝硬化和肝细胞癌发展的主要驱动因素。MASLD复杂的发病机制涉及脂质过度积累,随后扰乱脂质代谢并引发肝脏内炎症。本综述综合了在理解促成MASLD进展的机制方面的最新研究进展,特别强调代谢紊乱和器官间串扰。我们突出了与这些因素相关的分子机制,并探讨了它们作为药物干预新靶点的潜力。从本文中获得的见解对MASLD的预防和治疗管理都具有重要意义。