Liver Disease: From Gut Microbiota Dysbiosis and Metabolic Dysfunction to Inflammation, Fibrosis, and Hepatocellular Carcinoma

ABSTRACT BACKGROUND Liver diseases represent a major global health challenge, encompassing a broad spectrum of conditions ranging from metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) to chronic hepatitis, hepatic fibrosis, cirrhosis, and hepatocellular carcinoma. Increasing evidence suggests that liver disease progression involves complex interactions among metabolic disturbances, intestinal microbiota, immune responses, oxidative stress, and alterations in cellular homeostasis. The gut–liver axis represents an important biological interface through which intestinal microbial communities, microbial metabolites, and intestinal barrier integrity may influence hepatic physiology and disease progression. In particular, gut microbiota dysbiosis, increased intestinal permeability, and microbial-derived inflammatory mediators may contribute to chronic hepatic inflammation, metabolic dysfunction, and progressive tissue remodeling. Understanding these interconnected mechanisms may provide new perspectives on liver disease pathogenesis, prevention, and therapeutic strategies.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-11-09
DOI
https://doi.org/10.5281/zenodo.24090002
Primary Topic
Gut microbiota and health
Type
article
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article

Liver Disease: From Gut Microbiota Dysbiosis and Metabolic Dysfunction to Inflammation, Fibrosis, and Hepatocellular Carcinoma

Ivanildo dos Santos
Zenodo (CERN European Organization for Nuclear Research)
Gut microbiota and health
article

Liver Disease: From Gut Microbiota Dysbiosis and Metabolic Dysfunction to Inflammation, Fibrosis, and Hepatocellular Carcinoma

Ivanildo dos Santos
article en

Abstract

ABSTRACT BACKGROUND Liver diseases represent a major global health challenge, encompassing a broad spectrum of conditions ranging from metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) to chronic hepatitis, hepatic fibrosis, cirrhosis, and hepatocellular carcinoma. Increasing evidence suggests that liver disease progression involves complex interactions among metabolic disturbances, intestinal microbiota, immune responses, oxidative stress, and alterations in cellular homeostasis. The gut–liver axis represents an important biological interface through which intestinal microbial communities, microbial metabolites, and intestinal barrier integrity may influence hepatic physiology and disease progression. In particular, gut microbiota dysbiosis, increased intestinal permeability, and microbial-derived inflammatory mediators may contribute to chronic hepatic inflammation, metabolic dysfunction, and progressive tissue remodeling. Understanding these interconnected mechanisms may provide new perspectives on liver disease pathogenesis, prevention, and therapeutic strategies.

Zenodo (CERN European Organization for Nuclear Research)
Instituto Federal do Amapá (BR)
Gut microbiota and health
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