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Fecal Enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans

Type 2 diabetes (T2D) has been linked with increased intestinal permeability, but the clinical significance of this phenomenon remains unknown. The objective of this study was to investigate the potential link between glucose control, intestinal permeability, diet and intestinal microbiota in patien...

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Autores principales: Pedersen, Camilla, Ijaz, Umer Z., Gallagher, Edith, Horton, Felicity, Ellis, Richard J., Jaiyeola, Etana, Duparc, Thibaut, Russell‐Jones, David, Hinton, Paul, Cani, Patrice D., La Ragione, Roberto M., Robertson, M. Denise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880877/
https://www.ncbi.nlm.nih.gov/pubmed/29611319
http://dx.doi.org/10.14814/phy2.13649
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author Pedersen, Camilla
Ijaz, Umer Z.
Gallagher, Edith
Horton, Felicity
Ellis, Richard J.
Jaiyeola, Etana
Duparc, Thibaut
Russell‐Jones, David
Hinton, Paul
Cani, Patrice D.
La Ragione, Roberto M.
Robertson, M. Denise
author_facet Pedersen, Camilla
Ijaz, Umer Z.
Gallagher, Edith
Horton, Felicity
Ellis, Richard J.
Jaiyeola, Etana
Duparc, Thibaut
Russell‐Jones, David
Hinton, Paul
Cani, Patrice D.
La Ragione, Roberto M.
Robertson, M. Denise
author_sort Pedersen, Camilla
collection PubMed
description Type 2 diabetes (T2D) has been linked with increased intestinal permeability, but the clinical significance of this phenomenon remains unknown. The objective of this study was to investigate the potential link between glucose control, intestinal permeability, diet and intestinal microbiota in patients with T2D. Thirty‐two males with well‐controlled T2D and 30 age‐matched male controls without diabetes were enrolled in a case–control study. Metabolic parameters, inflammatory markers, endotoxemia, and intestinal microbiota in individuals subdivided into high (HP) and normal (LP) colonic permeability groups, were the main outcomes. In T2D, the HP group had significantly higher fasting glucose (P = 0.034) and plasma nonesterified fatty acid levels (P = 0.049) compared with the LP group. Increased colonic permeability was also linked with altered abundances of selected microbial taxa. The microbiota of both T2D and control HP groups was enriched with Enterobacteriales. In conclusion, high intestinal permeability was associated with poorer fasting glucose control in T2D patients and changes in some microbial taxa in both T2D patients and nondiabetic controls. Therefore, enrichment in the gram‐negative order Enterobacteriales may characterize impaired colonic permeability prior to/independently from a disruption in glucose tolerance.
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spelling pubmed-58808772018-04-04 Fecal Enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans Pedersen, Camilla Ijaz, Umer Z. Gallagher, Edith Horton, Felicity Ellis, Richard J. Jaiyeola, Etana Duparc, Thibaut Russell‐Jones, David Hinton, Paul Cani, Patrice D. La Ragione, Roberto M. Robertson, M. Denise Physiol Rep Original Research Type 2 diabetes (T2D) has been linked with increased intestinal permeability, but the clinical significance of this phenomenon remains unknown. The objective of this study was to investigate the potential link between glucose control, intestinal permeability, diet and intestinal microbiota in patients with T2D. Thirty‐two males with well‐controlled T2D and 30 age‐matched male controls without diabetes were enrolled in a case–control study. Metabolic parameters, inflammatory markers, endotoxemia, and intestinal microbiota in individuals subdivided into high (HP) and normal (LP) colonic permeability groups, were the main outcomes. In T2D, the HP group had significantly higher fasting glucose (P = 0.034) and plasma nonesterified fatty acid levels (P = 0.049) compared with the LP group. Increased colonic permeability was also linked with altered abundances of selected microbial taxa. The microbiota of both T2D and control HP groups was enriched with Enterobacteriales. In conclusion, high intestinal permeability was associated with poorer fasting glucose control in T2D patients and changes in some microbial taxa in both T2D patients and nondiabetic controls. Therefore, enrichment in the gram‐negative order Enterobacteriales may characterize impaired colonic permeability prior to/independently from a disruption in glucose tolerance. John Wiley and Sons Inc. 2018-04-02 /pmc/articles/PMC5880877/ /pubmed/29611319 http://dx.doi.org/10.14814/phy2.13649 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Pedersen, Camilla
Ijaz, Umer Z.
Gallagher, Edith
Horton, Felicity
Ellis, Richard J.
Jaiyeola, Etana
Duparc, Thibaut
Russell‐Jones, David
Hinton, Paul
Cani, Patrice D.
La Ragione, Roberto M.
Robertson, M. Denise
Fecal Enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans
title Fecal Enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans
title_full Fecal Enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans
title_fullStr Fecal Enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans
title_full_unstemmed Fecal Enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans
title_short Fecal Enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans
title_sort fecal enterobacteriales enrichment is associated with increased in vivo intestinal permeability in humans
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880877/
https://www.ncbi.nlm.nih.gov/pubmed/29611319
http://dx.doi.org/10.14814/phy2.13649
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