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Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease
Metabolic dysfunction-associated fatty liver disease (MAFLD) is a prevalent and challenging disease associated with a significant health and economic burden. MAFLD has been subjected to and widely investigated in many studies; however, the underlying pathogenesis and its progression have yet to unde...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683522/ https://www.ncbi.nlm.nih.gov/pubmed/38035056 http://dx.doi.org/10.4103/tcmj.tcmj_122_23 |
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author | Dongoran, Rachmad Anres Tu, Fang-Cen Liu, Chin-Hung |
author_facet | Dongoran, Rachmad Anres Tu, Fang-Cen Liu, Chin-Hung |
author_sort | Dongoran, Rachmad Anres |
collection | PubMed |
description | Metabolic dysfunction-associated fatty liver disease (MAFLD) is a prevalent and challenging disease associated with a significant health and economic burden. MAFLD has been subjected to and widely investigated in many studies; however, the underlying pathogenesis and its progression have yet to understand fully. Furthermore, precise biomarkers for diagnosing and specific drugs for treatment are yet to be discovered. Increasing evidence has proven gut microbiota as the neglected endocrine organ that regulates homeostasis and immune response. Targeting gut microbiota is an essential strategy for metabolic diseases, including MAFLD. Gut microbiota in the gut-liver axis is connected through tight bidirectional links through the biliary tract, portal vein, and systemic circulation, producing gut microbiota metabolites. This review focuses on the specific correlation between gut microbiota metabolites and MAFLD. Gut microbiota metabolites are biologically active in the host and, through subsequent changes and biological activities, provide implications for MAFLD. Based on the review studies, gut-liver axis related-metabolites including short-chain fatty acids, bile acids (BAs), lipopolysaccharide, choline and its metabolites, indole and its derivates, branched-chain amino acids, and methionine cycle derivates was associated with MAFLD and could be promising MAFLD diagnosis biomarkers, as well as the targets for MAFLD new drug discovery. |
format | Online Article Text |
id | pubmed-10683522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-106835222023-11-30 Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease Dongoran, Rachmad Anres Tu, Fang-Cen Liu, Chin-Hung Tzu Chi Med J Review Article Metabolic dysfunction-associated fatty liver disease (MAFLD) is a prevalent and challenging disease associated with a significant health and economic burden. MAFLD has been subjected to and widely investigated in many studies; however, the underlying pathogenesis and its progression have yet to understand fully. Furthermore, precise biomarkers for diagnosing and specific drugs for treatment are yet to be discovered. Increasing evidence has proven gut microbiota as the neglected endocrine organ that regulates homeostasis and immune response. Targeting gut microbiota is an essential strategy for metabolic diseases, including MAFLD. Gut microbiota in the gut-liver axis is connected through tight bidirectional links through the biliary tract, portal vein, and systemic circulation, producing gut microbiota metabolites. This review focuses on the specific correlation between gut microbiota metabolites and MAFLD. Gut microbiota metabolites are biologically active in the host and, through subsequent changes and biological activities, provide implications for MAFLD. Based on the review studies, gut-liver axis related-metabolites including short-chain fatty acids, bile acids (BAs), lipopolysaccharide, choline and its metabolites, indole and its derivates, branched-chain amino acids, and methionine cycle derivates was associated with MAFLD and could be promising MAFLD diagnosis biomarkers, as well as the targets for MAFLD new drug discovery. Wolters Kluwer - Medknow 2023-09-07 /pmc/articles/PMC10683522/ /pubmed/38035056 http://dx.doi.org/10.4103/tcmj.tcmj_122_23 Text en Copyright: © 2023 Tzu Chi Medical Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Article Dongoran, Rachmad Anres Tu, Fang-Cen Liu, Chin-Hung Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease |
title | Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease |
title_full | Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease |
title_fullStr | Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease |
title_full_unstemmed | Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease |
title_short | Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease |
title_sort | current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683522/ https://www.ncbi.nlm.nih.gov/pubmed/38035056 http://dx.doi.org/10.4103/tcmj.tcmj_122_23 |
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