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Fecal Microbiota Transplantation in NAFLD Treatment
Introduction: Gut microbiota is not only a taxonomic biologic ecosystem but is also involved in human intestinal and extra-intestinal functions such as immune system modulation, nutrient absorption and digestion, as well as metabolism regulation. The latter is strictly linked to non-alcoholic fatty...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695159/ https://www.ncbi.nlm.nih.gov/pubmed/36363516 http://dx.doi.org/10.3390/medicina58111559 |
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author | Abenavoli, Ludovico Maurizi, Valentina Rinninella, Emanuele Tack, Jan Di Berardino, Arianna Santori, Pierangelo Rasetti, Carlo Procopio, Anna Caterina Boccuto, Luigi Scarpellini, Emidio |
author_facet | Abenavoli, Ludovico Maurizi, Valentina Rinninella, Emanuele Tack, Jan Di Berardino, Arianna Santori, Pierangelo Rasetti, Carlo Procopio, Anna Caterina Boccuto, Luigi Scarpellini, Emidio |
author_sort | Abenavoli, Ludovico |
collection | PubMed |
description | Introduction: Gut microbiota is not only a taxonomic biologic ecosystem but is also involved in human intestinal and extra-intestinal functions such as immune system modulation, nutrient absorption and digestion, as well as metabolism regulation. The latter is strictly linked to non-alcoholic fatty liver disease (NAFLD) pathophysiology. Materials and methods: We reviewed the literature on the definition of gut microbiota, the concepts of “dysbiosis” and “eubiosis”, their role in NAFLD pathogenesis, and the data on fecal microbiota transplantation (FMT) in these patients. We consulted the main medical databases using the following keywords, acronyms, and their associations: gut microbiota, eubiosis, dysbiosis, bile acids, NAFLD, and FMT. Results: Gut microbiota qualitative and quantitative composition is different in healthy subjects vs. NALFD patients. This dysbiosis is associated with and involved in NAFLD pathogenesis and evolution to non-acoholic steatohepatitis (NASH), liver cirrhosis, and hepatocellular carcinoma (HCC). In detail, microbial-driven metabolism of bile acids (BAs) and interaction with hepatic and intestinal farnesoid nuclear X receptor (FXR) have shown a determinant role in liver fat deposition and the development of fibrosis. Over the use of pre- or probiotics, FMT has shown preclinical and initial clinical promising results in NAFLD treatment through re-modulation of microbial dysbiosis. Conclusions: Promising clinical data support a larger investigation of gut microbiota dysbiosis reversion through FMT in NAFLD using randomized clinical trials to design precision-medicine treatments for these patients at different disease stages. |
format | Online Article Text |
id | pubmed-9695159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96951592022-11-26 Fecal Microbiota Transplantation in NAFLD Treatment Abenavoli, Ludovico Maurizi, Valentina Rinninella, Emanuele Tack, Jan Di Berardino, Arianna Santori, Pierangelo Rasetti, Carlo Procopio, Anna Caterina Boccuto, Luigi Scarpellini, Emidio Medicina (Kaunas) Review Introduction: Gut microbiota is not only a taxonomic biologic ecosystem but is also involved in human intestinal and extra-intestinal functions such as immune system modulation, nutrient absorption and digestion, as well as metabolism regulation. The latter is strictly linked to non-alcoholic fatty liver disease (NAFLD) pathophysiology. Materials and methods: We reviewed the literature on the definition of gut microbiota, the concepts of “dysbiosis” and “eubiosis”, their role in NAFLD pathogenesis, and the data on fecal microbiota transplantation (FMT) in these patients. We consulted the main medical databases using the following keywords, acronyms, and their associations: gut microbiota, eubiosis, dysbiosis, bile acids, NAFLD, and FMT. Results: Gut microbiota qualitative and quantitative composition is different in healthy subjects vs. NALFD patients. This dysbiosis is associated with and involved in NAFLD pathogenesis and evolution to non-acoholic steatohepatitis (NASH), liver cirrhosis, and hepatocellular carcinoma (HCC). In detail, microbial-driven metabolism of bile acids (BAs) and interaction with hepatic and intestinal farnesoid nuclear X receptor (FXR) have shown a determinant role in liver fat deposition and the development of fibrosis. Over the use of pre- or probiotics, FMT has shown preclinical and initial clinical promising results in NAFLD treatment through re-modulation of microbial dysbiosis. Conclusions: Promising clinical data support a larger investigation of gut microbiota dysbiosis reversion through FMT in NAFLD using randomized clinical trials to design precision-medicine treatments for these patients at different disease stages. MDPI 2022-10-30 /pmc/articles/PMC9695159/ /pubmed/36363516 http://dx.doi.org/10.3390/medicina58111559 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Abenavoli, Ludovico Maurizi, Valentina Rinninella, Emanuele Tack, Jan Di Berardino, Arianna Santori, Pierangelo Rasetti, Carlo Procopio, Anna Caterina Boccuto, Luigi Scarpellini, Emidio Fecal Microbiota Transplantation in NAFLD Treatment |
title | Fecal Microbiota Transplantation in NAFLD Treatment |
title_full | Fecal Microbiota Transplantation in NAFLD Treatment |
title_fullStr | Fecal Microbiota Transplantation in NAFLD Treatment |
title_full_unstemmed | Fecal Microbiota Transplantation in NAFLD Treatment |
title_short | Fecal Microbiota Transplantation in NAFLD Treatment |
title_sort | fecal microbiota transplantation in nafld treatment |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695159/ https://www.ncbi.nlm.nih.gov/pubmed/36363516 http://dx.doi.org/10.3390/medicina58111559 |
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