Roles of short-chain fatty acids in metabolic dysfunction-associated steatotic liver disease and metabolic dysfunction-associated steatohepatitis
Роли короткоцепочечных жирных кислот при метаболически ассоциированном стеатотическом заболевании печени и метаболически ассоциированном стеатогепатите
2025-11-27
SCID: 54.1/xv9quaq4
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MASHMASLDSCFA modulation clinical trialsSCFAshepatic immune cellsinsulin sensitivitylipid and glucose metabolismliver fibrosisliver inflammationmetabolic dysfunction-associated steatohepatitismetabolic dysfunction-associated steatotic liver diseasemolecular signaling pathwaysshort-chain fatty acids
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Abstract (AI)
Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common chronic liver disease, affecting more than 30% of adults and 7%-14% of youths globally. MASLD and its advanced form of metabolic dysfunction-associated steatohepatitis (MASH) can progress to liver cirrhosis and hepatocellular carcinoma. Despite its growing burden, effective therapies for MASLD and MASH remain limited. Accumulating evidence indicates that short-chain fatty acids (SCFAs) modulate the activation of hepatic innate and adaptive immune cells, influencing liver inflammation and fibrosis. Moreover, SCFAs modulate liver lipid and glucose metabolism and insulin sensitivity, affecting MASLD progression. This review summarizes the cellular and molecular mechanisms through which SCFAs impact liver inflammation, fibrosis, and energy metabolism. Several key molecular signaling pathways are discussed. Clinical trials aiming to modulate SCFA production through different treatments are reviewed. Collectively, emerging evidence supports that targeting SCFA-mediated function represents a promising therapeutic strategy for MASLD and MASH.
Key Findings
1
Clinical trials that aim to modulate SCFA production through various treatments are underway, supporting therapeutic potential.
2
MASLD affects over 30% of adults and 7%-14% of youths worldwide, and can progress to cirrhosis and hepatocellular carcinoma.
3
SCFAs regulate liver lipid and glucose metabolism and insulin sensitivity, thereby affecting MASLD progression.
4
Short-chain fatty acids (SCFAs) modulate activation of hepatic innate and adaptive immune cells, influencing liver inflammation and fibrosis in MASLD/MASH.
5
Targeting SCFA-mediated functions is a promising therapeutic strategy for MASLD and MASH.
6
The review summarizes cellular and molecular mechanisms and key signaling pathways by which SCFAs impact liver inflammation, fibrosis, and energy metabolism.
Research Object
Short-chain fatty acids (SCFAs) in the context of metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH)
Research Subject
Roles and mechanisms by which SCFAs modulate liver inflammation, fibrosis, lipid and glucose metabolism, insulin sensitivity, and related molecular signaling pathways influencing MASLD/MASH progression and therapeutic potential
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2025-11-27
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