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Effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit

Acute intake of the wheat bran extract Arabinoxylan-Oligosaccharide (AXOS) modulates the gut microbiota, improves stool characteristics and postprandial glycemia in healthy humans. Yet, little is known on how long-term AXOS intake influences gastrointestinal (GI) functioning, gut microbiota, and met...

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Autores principales: Müller, Mattea, Hermes, Gerben D. A., Emanuel E., Canfora, Holst, Jens J., Zoetendal, Erwin G., Smidt, Hauke, Troost, Freddy, Schaap, Frank G., Damink, Steven Olde, Jocken, Johan W. E., Lenaerts, Kaatje, Masclee, Ad A. M., Blaak, Ellen E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524158/
https://www.ncbi.nlm.nih.gov/pubmed/31983281
http://dx.doi.org/10.1080/19490976.2019.1704141
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author Müller, Mattea
Hermes, Gerben D. A.
Emanuel E., Canfora
Holst, Jens J.
Zoetendal, Erwin G.
Smidt, Hauke
Troost, Freddy
Schaap, Frank G.
Damink, Steven Olde
Jocken, Johan W. E.
Lenaerts, Kaatje
Masclee, Ad A. M.
Blaak, Ellen E.
author_facet Müller, Mattea
Hermes, Gerben D. A.
Emanuel E., Canfora
Holst, Jens J.
Zoetendal, Erwin G.
Smidt, Hauke
Troost, Freddy
Schaap, Frank G.
Damink, Steven Olde
Jocken, Johan W. E.
Lenaerts, Kaatje
Masclee, Ad A. M.
Blaak, Ellen E.
author_sort Müller, Mattea
collection PubMed
description Acute intake of the wheat bran extract Arabinoxylan-Oligosaccharide (AXOS) modulates the gut microbiota, improves stool characteristics and postprandial glycemia in healthy humans. Yet, little is known on how long-term AXOS intake influences gastrointestinal (GI) functioning, gut microbiota, and metabolic health. In this randomized, placebo-controlled, double-blind study, we evaluated the effects of AXOS intake on GI function and metabolic health in adults with slow GI transit without constipation. Forty-eight normoglycemic adults were included with whole-gut transit time (WGTT) of >35 h receiving either 15 g/day AXOS or placebo (maltodextrin) for 12-wks. The primary outcome was WGTT, and secondary outcomes included stool parameters, gut permeability, short-chain fatty acids (SCFA), microbiota composition, energy expenditure, substrate oxidation, glucose, insulin, lipids, gut hormones, and adipose tissue (AT) function. WGTT was unchanged, but stool consistency softened after AXOS. 12-wks of AXOS intake significantly changed the microbiota by increasing Bifidobacterium and decreasing microbial alpha-diversity. With a good classification accuracy, overall microbiota composition classified responders with decreased WGTT after AXOS. The incretin hormone Glucagon-like protein 1 was reduced after AXOS compared to placebo. Energy expenditure, plasma metabolites, AT parameters, SCFA, and gut permeability were unchanged. In conclusion, intake of wheat bran extract increases fecal Bifidobacterium and softens stool consistency without major effects on energy metabolism in healthy humans with a slow GI transit. We show that overall gut microbiota classified responders with decreased WGTT after AXOS highlighting that GI transit and change thereof were associated with gut microbiota independent of Bifidobacterium. NCT02491125
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spelling pubmed-75241582020-10-06 Effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit Müller, Mattea Hermes, Gerben D. A. Emanuel E., Canfora Holst, Jens J. Zoetendal, Erwin G. Smidt, Hauke Troost, Freddy Schaap, Frank G. Damink, Steven Olde Jocken, Johan W. E. Lenaerts, Kaatje Masclee, Ad A. M. Blaak, Ellen E. Gut Microbes Research Paper Acute intake of the wheat bran extract Arabinoxylan-Oligosaccharide (AXOS) modulates the gut microbiota, improves stool characteristics and postprandial glycemia in healthy humans. Yet, little is known on how long-term AXOS intake influences gastrointestinal (GI) functioning, gut microbiota, and metabolic health. In this randomized, placebo-controlled, double-blind study, we evaluated the effects of AXOS intake on GI function and metabolic health in adults with slow GI transit without constipation. Forty-eight normoglycemic adults were included with whole-gut transit time (WGTT) of >35 h receiving either 15 g/day AXOS or placebo (maltodextrin) for 12-wks. The primary outcome was WGTT, and secondary outcomes included stool parameters, gut permeability, short-chain fatty acids (SCFA), microbiota composition, energy expenditure, substrate oxidation, glucose, insulin, lipids, gut hormones, and adipose tissue (AT) function. WGTT was unchanged, but stool consistency softened after AXOS. 12-wks of AXOS intake significantly changed the microbiota by increasing Bifidobacterium and decreasing microbial alpha-diversity. With a good classification accuracy, overall microbiota composition classified responders with decreased WGTT after AXOS. The incretin hormone Glucagon-like protein 1 was reduced after AXOS compared to placebo. Energy expenditure, plasma metabolites, AT parameters, SCFA, and gut permeability were unchanged. In conclusion, intake of wheat bran extract increases fecal Bifidobacterium and softens stool consistency without major effects on energy metabolism in healthy humans with a slow GI transit. We show that overall gut microbiota classified responders with decreased WGTT after AXOS highlighting that GI transit and change thereof were associated with gut microbiota independent of Bifidobacterium. NCT02491125 Taylor & Francis 2020-01-25 /pmc/articles/PMC7524158/ /pubmed/31983281 http://dx.doi.org/10.1080/19490976.2019.1704141 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. 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-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Müller, Mattea
Hermes, Gerben D. A.
Emanuel E., Canfora
Holst, Jens J.
Zoetendal, Erwin G.
Smidt, Hauke
Troost, Freddy
Schaap, Frank G.
Damink, Steven Olde
Jocken, Johan W. E.
Lenaerts, Kaatje
Masclee, Ad A. M.
Blaak, Ellen E.
Effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit
title Effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit
title_full Effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit
title_fullStr Effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit
title_full_unstemmed Effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit
title_short Effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit
title_sort effect of wheat bran derived prebiotic supplementation on gastrointestinal transit, gut microbiota, and metabolic health: a randomized controlled trial in healthy adults with a slow gut transit
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524158/
https://www.ncbi.nlm.nih.gov/pubmed/31983281
http://dx.doi.org/10.1080/19490976.2019.1704141
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