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Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis
The intestinal microbiota has been linked to the development and prevalence of steatohepatitis in humans. Interestingly, steatohepatitis is significantly lower in individuals taking a plant‐based, low‐animal‐protein diet, which is thought to be mediated by gut microbiota. However, data on causality...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603524/ https://www.ncbi.nlm.nih.gov/pubmed/33163830 http://dx.doi.org/10.1002/hep4.1601 |
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author | Witjes, Julia J. Smits, Loek P. Pekmez, Ceyda T. Prodan, Andrei Meijnikman, Abraham S. Troelstra, Marian A. Bouter, Kristien E.C. Herrema, Hilde Levin, Evgeni Holleboom, Adriaan G. Winkelmeijer, Maaike Beuers, Ulrich H. van Lienden, Krijn Aron‐Wisnewky, Judith Mannisto, Ville Bergman, Jacques J. Runge, Jurgen H. Nederveen, Aart J. Dragsted, Lars O. Konstanti, Prokopis Zoetendal, Erwin G. de Vos, Willem Verheij, Joanne Groen, Albert K. Nieuwdorp, Max |
author_facet | Witjes, Julia J. Smits, Loek P. Pekmez, Ceyda T. Prodan, Andrei Meijnikman, Abraham S. Troelstra, Marian A. Bouter, Kristien E.C. Herrema, Hilde Levin, Evgeni Holleboom, Adriaan G. Winkelmeijer, Maaike Beuers, Ulrich H. van Lienden, Krijn Aron‐Wisnewky, Judith Mannisto, Ville Bergman, Jacques J. Runge, Jurgen H. Nederveen, Aart J. Dragsted, Lars O. Konstanti, Prokopis Zoetendal, Erwin G. de Vos, Willem Verheij, Joanne Groen, Albert K. Nieuwdorp, Max |
author_sort | Witjes, Julia J. |
collection | PubMed |
description | The intestinal microbiota has been linked to the development and prevalence of steatohepatitis in humans. Interestingly, steatohepatitis is significantly lower in individuals taking a plant‐based, low‐animal‐protein diet, which is thought to be mediated by gut microbiota. However, data on causality between these observations in humans is scarce. In this regard, fecal microbiota transplantation (FMT) using healthy donors is safe and is capable of changing microbial composition in human disease. We therefore performed a double‐blind randomized controlled proof‐of‐principle study in which individuals with hepatic steatosis on ultrasound were randomized to two study arms: lean vegan donor (allogenic n = 10) or own (autologous n = 11) FMT. Both were performed three times at 8‐week intervals. A liver biopsy was performed at baseline and after 24 weeks in every subject to determine histopathology (Nonalcoholic Steatohepatitis Clinical Research Network) classification and changes in hepatic gene expression based on RNA sequencing. Secondary outcome parameters were changes in intestinal microbiota composition and fasting plasma metabolomics. We observed a trend toward improved necro‐inflammatory histology, and found significant changes in expression of hepatic genes involved in inflammation and lipid metabolism following allogenic FMT. Intestinal microbial community structure changed following allogenic FMT, which was associated with changes in plasma metabolites as well as markers of . Conclusion: Allogenic FMT using lean vegan donors in individuals with hepatic steatosis shows an effect on intestinal microbiota composition, which is associated with beneficial changes in plasma metabolites and markers of steatohepatitis. |
format | Online Article Text |
id | pubmed-7603524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76035242020-11-05 Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis Witjes, Julia J. Smits, Loek P. Pekmez, Ceyda T. Prodan, Andrei Meijnikman, Abraham S. Troelstra, Marian A. Bouter, Kristien E.C. Herrema, Hilde Levin, Evgeni Holleboom, Adriaan G. Winkelmeijer, Maaike Beuers, Ulrich H. van Lienden, Krijn Aron‐Wisnewky, Judith Mannisto, Ville Bergman, Jacques J. Runge, Jurgen H. Nederveen, Aart J. Dragsted, Lars O. Konstanti, Prokopis Zoetendal, Erwin G. de Vos, Willem Verheij, Joanne Groen, Albert K. Nieuwdorp, Max Hepatol Commun Original Articles The intestinal microbiota has been linked to the development and prevalence of steatohepatitis in humans. Interestingly, steatohepatitis is significantly lower in individuals taking a plant‐based, low‐animal‐protein diet, which is thought to be mediated by gut microbiota. However, data on causality between these observations in humans is scarce. In this regard, fecal microbiota transplantation (FMT) using healthy donors is safe and is capable of changing microbial composition in human disease. We therefore performed a double‐blind randomized controlled proof‐of‐principle study in which individuals with hepatic steatosis on ultrasound were randomized to two study arms: lean vegan donor (allogenic n = 10) or own (autologous n = 11) FMT. Both were performed three times at 8‐week intervals. A liver biopsy was performed at baseline and after 24 weeks in every subject to determine histopathology (Nonalcoholic Steatohepatitis Clinical Research Network) classification and changes in hepatic gene expression based on RNA sequencing. Secondary outcome parameters were changes in intestinal microbiota composition and fasting plasma metabolomics. We observed a trend toward improved necro‐inflammatory histology, and found significant changes in expression of hepatic genes involved in inflammation and lipid metabolism following allogenic FMT. Intestinal microbial community structure changed following allogenic FMT, which was associated with changes in plasma metabolites as well as markers of . Conclusion: Allogenic FMT using lean vegan donors in individuals with hepatic steatosis shows an effect on intestinal microbiota composition, which is associated with beneficial changes in plasma metabolites and markers of steatohepatitis. John Wiley and Sons Inc. 2020-10-07 /pmc/articles/PMC7603524/ /pubmed/33163830 http://dx.doi.org/10.1002/hep4.1601 Text en © 2020 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Witjes, Julia J. Smits, Loek P. Pekmez, Ceyda T. Prodan, Andrei Meijnikman, Abraham S. Troelstra, Marian A. Bouter, Kristien E.C. Herrema, Hilde Levin, Evgeni Holleboom, Adriaan G. Winkelmeijer, Maaike Beuers, Ulrich H. van Lienden, Krijn Aron‐Wisnewky, Judith Mannisto, Ville Bergman, Jacques J. Runge, Jurgen H. Nederveen, Aart J. Dragsted, Lars O. Konstanti, Prokopis Zoetendal, Erwin G. de Vos, Willem Verheij, Joanne Groen, Albert K. Nieuwdorp, Max Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis |
title | Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis |
title_full | Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis |
title_fullStr | Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis |
title_full_unstemmed | Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis |
title_short | Donor Fecal Microbiota Transplantation Alters Gut Microbiota and Metabolites in Obese Individuals With Steatohepatitis |
title_sort | donor fecal microbiota transplantation alters gut microbiota and metabolites in obese individuals with steatohepatitis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603524/ https://www.ncbi.nlm.nih.gov/pubmed/33163830 http://dx.doi.org/10.1002/hep4.1601 |
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