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Exocrine Pancreatic Function Modulates Plasma Metabolites Through Changes in Gut Microbiota Composition
PURPOSE: Exocrine pancreatic function is critically involved in regulating the gut microbiota composition. At the same time, its impairment acutely affects human metabolism. How these 2 roles are connected is unknown. We studied how the exocrine pancreas contributes to metabolism via modulation of g...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186556/ https://www.ncbi.nlm.nih.gov/pubmed/33462612 http://dx.doi.org/10.1210/clinem/dgaa961 |
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author | Pietzner, Maik Budde, Kathrin Rühlemann, Malte Völzke, Henry Homuth, Georg Weiss, Frank U Lerch, Markus M Frost, Fabian |
author_facet | Pietzner, Maik Budde, Kathrin Rühlemann, Malte Völzke, Henry Homuth, Georg Weiss, Frank U Lerch, Markus M Frost, Fabian |
author_sort | Pietzner, Maik |
collection | PubMed |
description | PURPOSE: Exocrine pancreatic function is critically involved in regulating the gut microbiota composition. At the same time, its impairment acutely affects human metabolism. How these 2 roles are connected is unknown. We studied how the exocrine pancreas contributes to metabolism via modulation of gut microbiota. DESIGN: Fecal samples were collected in 2226 participants of the population-based Study of Health in Pomerania (SHIP/SHIP-TREND) to determine exocrine pancreatic function (pancreatic elastase enzyme-linked immunosorbent assay) and intestinal microbiota profiles (16S ribosomal ribonucleic acid gene sequencing). Plasma metabolite levels were determined by mass spectrometry. RESULTS: Exocrine pancreatic function was associated with changes in the abundance of 28 taxa and, simultaneously, with those of 16 plasma metabolites. Mediation pathway analysis revealed that a significant component of how exocrine pancreatic function affects the blood metabolome is mediated via gut microbiota abundance changes, most prominently, circulating serotonin and lysophosphatidylcholines. CONCLUSION: These results imply that the effect of exocrine pancreatic function on intestinal microbiota composition alters the availability of microbial-derived metabolites in the blood and thus directly contributes to the host metabolic changes associated with exocrine pancreatic dysfunction. |
format | Online Article Text |
id | pubmed-8186556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81865562021-06-10 Exocrine Pancreatic Function Modulates Plasma Metabolites Through Changes in Gut Microbiota Composition Pietzner, Maik Budde, Kathrin Rühlemann, Malte Völzke, Henry Homuth, Georg Weiss, Frank U Lerch, Markus M Frost, Fabian J Clin Endocrinol Metab Clinical Research Articles PURPOSE: Exocrine pancreatic function is critically involved in regulating the gut microbiota composition. At the same time, its impairment acutely affects human metabolism. How these 2 roles are connected is unknown. We studied how the exocrine pancreas contributes to metabolism via modulation of gut microbiota. DESIGN: Fecal samples were collected in 2226 participants of the population-based Study of Health in Pomerania (SHIP/SHIP-TREND) to determine exocrine pancreatic function (pancreatic elastase enzyme-linked immunosorbent assay) and intestinal microbiota profiles (16S ribosomal ribonucleic acid gene sequencing). Plasma metabolite levels were determined by mass spectrometry. RESULTS: Exocrine pancreatic function was associated with changes in the abundance of 28 taxa and, simultaneously, with those of 16 plasma metabolites. Mediation pathway analysis revealed that a significant component of how exocrine pancreatic function affects the blood metabolome is mediated via gut microbiota abundance changes, most prominently, circulating serotonin and lysophosphatidylcholines. CONCLUSION: These results imply that the effect of exocrine pancreatic function on intestinal microbiota composition alters the availability of microbial-derived metabolites in the blood and thus directly contributes to the host metabolic changes associated with exocrine pancreatic dysfunction. Oxford University Press 2021-01-19 /pmc/articles/PMC8186556/ /pubmed/33462612 http://dx.doi.org/10.1210/clinem/dgaa961 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Clinical Research Articles Pietzner, Maik Budde, Kathrin Rühlemann, Malte Völzke, Henry Homuth, Georg Weiss, Frank U Lerch, Markus M Frost, Fabian Exocrine Pancreatic Function Modulates Plasma Metabolites Through Changes in Gut Microbiota Composition |
title | Exocrine Pancreatic Function Modulates Plasma Metabolites Through
Changes in Gut Microbiota Composition |
title_full | Exocrine Pancreatic Function Modulates Plasma Metabolites Through
Changes in Gut Microbiota Composition |
title_fullStr | Exocrine Pancreatic Function Modulates Plasma Metabolites Through
Changes in Gut Microbiota Composition |
title_full_unstemmed | Exocrine Pancreatic Function Modulates Plasma Metabolites Through
Changes in Gut Microbiota Composition |
title_short | Exocrine Pancreatic Function Modulates Plasma Metabolites Through
Changes in Gut Microbiota Composition |
title_sort | exocrine pancreatic function modulates plasma metabolites through
changes in gut microbiota composition |
topic | Clinical Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186556/ https://www.ncbi.nlm.nih.gov/pubmed/33462612 http://dx.doi.org/10.1210/clinem/dgaa961 |
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