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April 26, 2026Journal of Clinical and Translational Hepatology1 citationsOpen Access

The Multifaceted Roles of Gut Microbiota and Their Metabolites in Metabolic Dysfunction-associated Steatotic Liver Disease: A Literature Review

YZYunqi ZhangDWDengqin WangBZBo Zhuang

Key Points

  • This review aims to explore the complex roles of gut microbiota and their metabolites in metabolic dysfunction-associated steatotic liver disease (MASLD).
  • Literature review synthesizing existing evidence on gut microbiota's effects in MASLD.
  • Delineation of the gut-liver axis and its interactions with hepatic metabolism and immune responses.
  • Analysis of both beneficial and detrimental impacts of gut microbial communities on disease progression.
  • Gut microbiota dysbiosis contributes to liver steatosis and has potential implications for disease severity.
  • Evidence supports the gut-liver axis as a critical factor in regulating oxidative stress and metabolic reprogramming.
  • Findings may guide microbiome-based interventions to improve MASLD outcomes.

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) represents a major global health concern and encompasses a spectrum ranging from hepatic steatosis and metabolic dysfunction-associated steatohepatitis to liver fibrosis, cirrhosis, and ultimately hepatocellular carcinoma. Insulin resistance, the pathogenic cornerstone of MASLD, drives enhanced peripheral lipolysis and increased hepatic de novo lipogenesis, thereby overloading the liver with lipids and inducing steatosis. Subsequent lipotoxicity, inflammation, and gut microbiota dysbiosis further exacerbate disease progression. The gut microbiota and their metabolites communicate with the liver via the gut-liver axis, forming a complex signaling network that directly or indirectly modulates hepatic metabolism, systemic immune responses, oxidative stress, and intestinal barrier integrity. In this review, we synthesize evidence for the beneficial and detrimental effects of the major human gut microbial communities and their metabolites during the course of MASLD. We delineate how these gut-derived factors regulate hepatic function through an integrated tripartite “gut-liver axis–oxidative stress–metabolic reprogramming” mechanism. These insights may inform microbiome-based precision interventions and accelerate the development of therapeutic strategies targeting MASLD.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/69edabb84a46254e215b3a44https://doi.org/10.14218/jcth.2025.00605
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