Key result
Lipotoxicity drives MASLD pathogenesis by promoting liver inflammation and fibrogenesis.
This review provides a comprehensive overview of how lipotoxicity drives the pathogenesis of MASLD and highlights potential therapeutic strategies targeting lipid metabolism.
Metabolic dysfunction-associated steatotic liver disease (MASLD) encompasses a spectrum of liver lesions, ranging from simple steatosis to metabolic dysfunction-associated steatohepatitis (MASH), that may further progress to cirrhosis. MASLD is estimated to affect more than one third of the general population and it represents a risk factor for end-stage liver failure and liver cancer, substantially contributing to liver-related morbidity and mortality. Although the pathogenesis of MASLD is incompletely understood, it is known to consist of a multifactorial process influenced by extrinsic and intrinsic factors such as metabolic, environmental and demographic features, gut microbiota and genetics. Dysregulation of both extracellular and intracellular lipid composition is known to promote the generation of toxic lipid species, thereby triggering lipotoxicity and cellular stress. These events ultimately lead to the activation of distinct cell death pathways, resulting in inflammation, fibrogenesis and, eventually, carcinogenesis. In this manuscript, we provide a comprehensive review of the role of lipotoxicity during MASLD pathogenesis, discussing the most relevant lipid species and related molecular mechanisms, summarizing the cell type-specific effects and highlighting the most promising putative therapeutic strategies for modulating lipotoxicity and lipid metabolism in MASLD.
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Iturbe-Rey et al. (2024) conducted a review in Metabolic dysfunction-associated steatotic liver disease (MASLD). Lipotoxicity and dysregulation of lipid composition play a central role in the pathogenesis of metabolic dysfunction-associated steatotic liver disease, driving inflammation and fibrogenesis.
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