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A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation
Several characteristic features of the fecal microbiota have been described in primary sclerosing cholangitis (PSC), whereas data on mucosal microbiota are less consistent. We aimed to use a large colonoscopy cohort to investigate key knowledge gaps, including the role of gut microbiota in PSC with...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936983/ https://www.ncbi.nlm.nih.gov/pubmed/36056902 http://dx.doi.org/10.1002/hep.32773 |
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author | Hole, Mikal Jacob Jørgensen, Kristin Kaasen Holm, Kristian Braadland, Peder R. Meyer‐Myklestad, Malin Holm Medhus, Asle Wilhelm Reikvam, Dag Henrik Götz, Alexandra Grzyb, Krzysztof Boberg, Kirsten Muri Karlsen, Tom Hemming Kummen, Martin Hov, Johannes R. |
author_facet | Hole, Mikal Jacob Jørgensen, Kristin Kaasen Holm, Kristian Braadland, Peder R. Meyer‐Myklestad, Malin Holm Medhus, Asle Wilhelm Reikvam, Dag Henrik Götz, Alexandra Grzyb, Krzysztof Boberg, Kirsten Muri Karlsen, Tom Hemming Kummen, Martin Hov, Johannes R. |
author_sort | Hole, Mikal Jacob |
collection | PubMed |
description | Several characteristic features of the fecal microbiota have been described in primary sclerosing cholangitis (PSC), whereas data on mucosal microbiota are less consistent. We aimed to use a large colonoscopy cohort to investigate key knowledge gaps, including the role of gut microbiota in PSC with inflammatory bowel disease (IBD), the effect of liver transplantation (LT), and whether recurrent PSC (rPSC) may be used to define consistent microbiota features in PSC irrespective of LT. APPROACH AND RESULTS: We included 84 PSC and 51 liver transplanted PSC patients (PSC‐LT) and 40 healthy controls (HCs) and performed sequencing of the 16S ribosomal RNA gene (V3–V4) from ileocolonic biopsies. Intraindividual microbial diversity was reduced in both PSC and PSC‐LT versus HCs. An expansion of Proteobacteria was more pronounced in PSC‐LT (up to 19% relative abundance) than in PSC (up to 11%) and HCs (up to 8%; Q(FDR) < 0.05). When investigating PSC before (PSC vs. HC) and after LT (rPSC vs. no‐rPSC), increased variability (dispersion) in the PSC group was found. Five genera were associated with PSC before and after LT. A dysbiosis index calculated from the five genera, and the presence of the potential pathobiont, Klebsiella, were associated with reduced LT‐free survival. Concomitant IBD was associated with reduced Akkermansia. CONCLUSIONS: Consistent mucosal microbiota features associated with PSC, PSC‐IBD, and disease severity, irrespective of LT status, highlight the usefulness of investigating PSC and rPSC in parallel, and suggest that the impact of gut microbiota on posttransplant liver health should be investigated further. |
format | Online Article Text |
id | pubmed-9936983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-99369832023-02-18 A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation Hole, Mikal Jacob Jørgensen, Kristin Kaasen Holm, Kristian Braadland, Peder R. Meyer‐Myklestad, Malin Holm Medhus, Asle Wilhelm Reikvam, Dag Henrik Götz, Alexandra Grzyb, Krzysztof Boberg, Kirsten Muri Karlsen, Tom Hemming Kummen, Martin Hov, Johannes R. Hepatology Original Articles: Immune-Mediated Diseases Several characteristic features of the fecal microbiota have been described in primary sclerosing cholangitis (PSC), whereas data on mucosal microbiota are less consistent. We aimed to use a large colonoscopy cohort to investigate key knowledge gaps, including the role of gut microbiota in PSC with inflammatory bowel disease (IBD), the effect of liver transplantation (LT), and whether recurrent PSC (rPSC) may be used to define consistent microbiota features in PSC irrespective of LT. APPROACH AND RESULTS: We included 84 PSC and 51 liver transplanted PSC patients (PSC‐LT) and 40 healthy controls (HCs) and performed sequencing of the 16S ribosomal RNA gene (V3–V4) from ileocolonic biopsies. Intraindividual microbial diversity was reduced in both PSC and PSC‐LT versus HCs. An expansion of Proteobacteria was more pronounced in PSC‐LT (up to 19% relative abundance) than in PSC (up to 11%) and HCs (up to 8%; Q(FDR) < 0.05). When investigating PSC before (PSC vs. HC) and after LT (rPSC vs. no‐rPSC), increased variability (dispersion) in the PSC group was found. Five genera were associated with PSC before and after LT. A dysbiosis index calculated from the five genera, and the presence of the potential pathobiont, Klebsiella, were associated with reduced LT‐free survival. Concomitant IBD was associated with reduced Akkermansia. CONCLUSIONS: Consistent mucosal microbiota features associated with PSC, PSC‐IBD, and disease severity, irrespective of LT status, highlight the usefulness of investigating PSC and rPSC in parallel, and suggest that the impact of gut microbiota on posttransplant liver health should be investigated further. Lippincott Williams & Wilkins 2023-03 2023-02-17 /pmc/articles/PMC9936983/ /pubmed/36056902 http://dx.doi.org/10.1002/hep.32773 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Articles: Immune-Mediated Diseases Hole, Mikal Jacob Jørgensen, Kristin Kaasen Holm, Kristian Braadland, Peder R. Meyer‐Myklestad, Malin Holm Medhus, Asle Wilhelm Reikvam, Dag Henrik Götz, Alexandra Grzyb, Krzysztof Boberg, Kirsten Muri Karlsen, Tom Hemming Kummen, Martin Hov, Johannes R. A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation |
title | A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation |
title_full | A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation |
title_fullStr | A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation |
title_full_unstemmed | A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation |
title_short | A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation |
title_sort | shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation |
topic | Original Articles: Immune-Mediated Diseases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936983/ https://www.ncbi.nlm.nih.gov/pubmed/36056902 http://dx.doi.org/10.1002/hep.32773 |
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