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A study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans

Introduction: A major component of the digesta reaching the colon from the distal ileum is carbohydrate. This carbohydrate is subject to microbial fermentation and can radically change bacterial populations in the colon and the metabolites they produce, particularly short-chain fatty acids (SCFA). H...

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Autores principales: Byrne, Claire S., Blunt, Dominic, Burn, James, Chambers, Edward, Dagbasi, Aygul, Franco Becker, Georgia, Gibson, Glenn, Mendoza, Lilian, Murphy, Kevin, Poveda, Carlos, Ramgulam, Anya, Tashkova, Martina, Walton, Gemma, Washirasaksiri, Chaiwat, Frost, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904985/
https://www.ncbi.nlm.nih.gov/pubmed/31857893
http://dx.doi.org/10.12688/f1000research.17870.2
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author Byrne, Claire S.
Blunt, Dominic
Burn, James
Chambers, Edward
Dagbasi, Aygul
Franco Becker, Georgia
Gibson, Glenn
Mendoza, Lilian
Murphy, Kevin
Poveda, Carlos
Ramgulam, Anya
Tashkova, Martina
Walton, Gemma
Washirasaksiri, Chaiwat
Frost, Gary
author_facet Byrne, Claire S.
Blunt, Dominic
Burn, James
Chambers, Edward
Dagbasi, Aygul
Franco Becker, Georgia
Gibson, Glenn
Mendoza, Lilian
Murphy, Kevin
Poveda, Carlos
Ramgulam, Anya
Tashkova, Martina
Walton, Gemma
Washirasaksiri, Chaiwat
Frost, Gary
author_sort Byrne, Claire S.
collection PubMed
description Introduction: A major component of the digesta reaching the colon from the distal ileum is carbohydrate. This carbohydrate is subject to microbial fermentation and can radically change bacterial populations in the colon and the metabolites they produce, particularly short-chain fatty acids (SCFA). However, very little is currently known about the forms and levels of carbohydrate in the ileum and the composition of the ileal microbiota in humans. Most of our current understanding of carbohydrate that is not absorbed by the small intestine comes from ileostomy models, which may not reflect the physiology of an intact gastrointestinal tract. Methods: We will investigate how ileal content changes depending on diet using a randomised crossover study in healthy humans. Participants will be inpatients at the research facility for three separate 4-day visits. During each visit, participants will consume one of three diets, which differ in carbohydrate quality: 1) low-fibre refined diet; 2) high-fibre diet with intact cellular structures; 3) high-fibre diet where the cellular structures have been disrupted (e.g. milling, blending). On day 1, a nasoenteric tube will be placed into the distal ileum and its position confirmed under fluoroscopy. Ileal samples will be collected via the nasoenteric tube and metabolically profiled, which will determine the amount and type of carbohydrate present, and the composition of the ileal microbiota will be measured. Blood samples will be collected to assess circulating hormones and metabolites. Stool samples will be collected to assess faecal microbiota composition. Subjective appetite measures will be collected using visual analogue scales. Breath hydrogen will be measured in real-time as a marker of intestinal fermentation. Finally, an in vitro continuous fermentation model will be inoculated with ileal fluid in order to understand the shift in microbial composition and SCFA produced in the colon following the different diets. Registration: ISRCTN11327221.
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spelling pubmed-69049852019-12-18 A study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans Byrne, Claire S. Blunt, Dominic Burn, James Chambers, Edward Dagbasi, Aygul Franco Becker, Georgia Gibson, Glenn Mendoza, Lilian Murphy, Kevin Poveda, Carlos Ramgulam, Anya Tashkova, Martina Walton, Gemma Washirasaksiri, Chaiwat Frost, Gary F1000Res Study Protocol Introduction: A major component of the digesta reaching the colon from the distal ileum is carbohydrate. This carbohydrate is subject to microbial fermentation and can radically change bacterial populations in the colon and the metabolites they produce, particularly short-chain fatty acids (SCFA). However, very little is currently known about the forms and levels of carbohydrate in the ileum and the composition of the ileal microbiota in humans. Most of our current understanding of carbohydrate that is not absorbed by the small intestine comes from ileostomy models, which may not reflect the physiology of an intact gastrointestinal tract. Methods: We will investigate how ileal content changes depending on diet using a randomised crossover study in healthy humans. Participants will be inpatients at the research facility for three separate 4-day visits. During each visit, participants will consume one of three diets, which differ in carbohydrate quality: 1) low-fibre refined diet; 2) high-fibre diet with intact cellular structures; 3) high-fibre diet where the cellular structures have been disrupted (e.g. milling, blending). On day 1, a nasoenteric tube will be placed into the distal ileum and its position confirmed under fluoroscopy. Ileal samples will be collected via the nasoenteric tube and metabolically profiled, which will determine the amount and type of carbohydrate present, and the composition of the ileal microbiota will be measured. Blood samples will be collected to assess circulating hormones and metabolites. Stool samples will be collected to assess faecal microbiota composition. Subjective appetite measures will be collected using visual analogue scales. Breath hydrogen will be measured in real-time as a marker of intestinal fermentation. Finally, an in vitro continuous fermentation model will be inoculated with ileal fluid in order to understand the shift in microbial composition and SCFA produced in the colon following the different diets. Registration: ISRCTN11327221. F1000 Research Limited 2019-10-22 /pmc/articles/PMC6904985/ /pubmed/31857893 http://dx.doi.org/10.12688/f1000research.17870.2 Text en Copyright: © 2019 Byrne CS et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Byrne, Claire S.
Blunt, Dominic
Burn, James
Chambers, Edward
Dagbasi, Aygul
Franco Becker, Georgia
Gibson, Glenn
Mendoza, Lilian
Murphy, Kevin
Poveda, Carlos
Ramgulam, Anya
Tashkova, Martina
Walton, Gemma
Washirasaksiri, Chaiwat
Frost, Gary
A study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans
title A study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans
title_full A study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans
title_fullStr A study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans
title_full_unstemmed A study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans
title_short A study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans
title_sort study protocol for a randomised crossover study evaluating the effect of diets differing in carbohydrate quality on ileal content and appetite regulation in healthy humans
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904985/
https://www.ncbi.nlm.nih.gov/pubmed/31857893
http://dx.doi.org/10.12688/f1000research.17870.2
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