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Impact of dietary supplementation with resistant dextrin (NUTRIOSE(®)) on satiety, glycaemia, and related endpoints, in healthy adults

PURPOSE: Resistant dextrin (RD) supplementation has been shown to alter satiety, glycaemia, and body weight, in overweight Chinese men; however, there are limited data on its effects in other demographic groups. Here, we investigated the effects of RD on satiety in healthy adults living in the Unite...

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Autores principales: Hobden, Mark R., Commane, Daniel M., Guérin-Deremaux, Laetitia, Wils, Daniel, Thabuis, Clementine, Martin-Morales, Agustin, Wolfram, Saskia, Dìaz, Antonio, Collins, Sineaid, Morais, Ines, Rowland, Ian R., Gibson, Glenn R., Kennedy, Orla B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572182/
https://www.ncbi.nlm.nih.gov/pubmed/34170392
http://dx.doi.org/10.1007/s00394-021-02618-9
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author Hobden, Mark R.
Commane, Daniel M.
Guérin-Deremaux, Laetitia
Wils, Daniel
Thabuis, Clementine
Martin-Morales, Agustin
Wolfram, Saskia
Dìaz, Antonio
Collins, Sineaid
Morais, Ines
Rowland, Ian R.
Gibson, Glenn R.
Kennedy, Orla B.
author_facet Hobden, Mark R.
Commane, Daniel M.
Guérin-Deremaux, Laetitia
Wils, Daniel
Thabuis, Clementine
Martin-Morales, Agustin
Wolfram, Saskia
Dìaz, Antonio
Collins, Sineaid
Morais, Ines
Rowland, Ian R.
Gibson, Glenn R.
Kennedy, Orla B.
author_sort Hobden, Mark R.
collection PubMed
description PURPOSE: Resistant dextrin (RD) supplementation has been shown to alter satiety, glycaemia, and body weight, in overweight Chinese men; however, there are limited data on its effects in other demographic groups. Here, we investigated the effects of RD on satiety in healthy adults living in the United Kingdom. METHODS: 20 normal weight and 16 overweight adults completed this randomised controlled cross-over study. Either RD (14 g/day NUTRIOSE(®) FB06) or maltodextrin control was consumed in mid-morning and mid-afternoon preload beverages over a 28-day treatment period with crossover after a 28-day washout. During 10-h study visits (on days 1, 14, and 28 of each treatment period), satietogenic, glycaemic and anorectic hormonal responses to provided meals were assessed. RESULTS: Chronic supplementation with RD was associated with higher fasted satiety scores at day 14 (P = 0.006) and day 28 (P = 0.040), compared to control. RD also increased satiety after the mid-morning intervention drink, but it was associated with a reduction in post-meal satiety following both the lunch and evening meals (P < 0.01). The glycaemic response to the mid-morning intervention drink (0–30 min) was attenuated following RD supplementation (P < 0.01). Whilst not a primary endpoint we also observed lower systolic blood pressure at day 14 (P = 0.035) and 28 (P = 0.030), compared to day 1, following RD supplementation in the normal weight group. Energy intake and anthropometrics were unaffected. CONCLUSIONS: RD supplementation modified satiety and glycaemic responses in this cohort, further studies are required to determine longer-term effects on body weight control and metabolic markers. CLINICALTRIALS.GOV REGISTRATION: NCT02041975 (22/01/2014) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00394-021-02618-9.
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spelling pubmed-85721822021-11-15 Impact of dietary supplementation with resistant dextrin (NUTRIOSE(®)) on satiety, glycaemia, and related endpoints, in healthy adults Hobden, Mark R. Commane, Daniel M. Guérin-Deremaux, Laetitia Wils, Daniel Thabuis, Clementine Martin-Morales, Agustin Wolfram, Saskia Dìaz, Antonio Collins, Sineaid Morais, Ines Rowland, Ian R. Gibson, Glenn R. Kennedy, Orla B. Eur J Nutr Original Contribution PURPOSE: Resistant dextrin (RD) supplementation has been shown to alter satiety, glycaemia, and body weight, in overweight Chinese men; however, there are limited data on its effects in other demographic groups. Here, we investigated the effects of RD on satiety in healthy adults living in the United Kingdom. METHODS: 20 normal weight and 16 overweight adults completed this randomised controlled cross-over study. Either RD (14 g/day NUTRIOSE(®) FB06) or maltodextrin control was consumed in mid-morning and mid-afternoon preload beverages over a 28-day treatment period with crossover after a 28-day washout. During 10-h study visits (on days 1, 14, and 28 of each treatment period), satietogenic, glycaemic and anorectic hormonal responses to provided meals were assessed. RESULTS: Chronic supplementation with RD was associated with higher fasted satiety scores at day 14 (P = 0.006) and day 28 (P = 0.040), compared to control. RD also increased satiety after the mid-morning intervention drink, but it was associated with a reduction in post-meal satiety following both the lunch and evening meals (P < 0.01). The glycaemic response to the mid-morning intervention drink (0–30 min) was attenuated following RD supplementation (P < 0.01). Whilst not a primary endpoint we also observed lower systolic blood pressure at day 14 (P = 0.035) and 28 (P = 0.030), compared to day 1, following RD supplementation in the normal weight group. Energy intake and anthropometrics were unaffected. CONCLUSIONS: RD supplementation modified satiety and glycaemic responses in this cohort, further studies are required to determine longer-term effects on body weight control and metabolic markers. CLINICALTRIALS.GOV REGISTRATION: NCT02041975 (22/01/2014) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00394-021-02618-9. Springer Berlin Heidelberg 2021-06-25 2021 /pmc/articles/PMC8572182/ /pubmed/34170392 http://dx.doi.org/10.1007/s00394-021-02618-9 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Contribution
Hobden, Mark R.
Commane, Daniel M.
Guérin-Deremaux, Laetitia
Wils, Daniel
Thabuis, Clementine
Martin-Morales, Agustin
Wolfram, Saskia
Dìaz, Antonio
Collins, Sineaid
Morais, Ines
Rowland, Ian R.
Gibson, Glenn R.
Kennedy, Orla B.
Impact of dietary supplementation with resistant dextrin (NUTRIOSE(®)) on satiety, glycaemia, and related endpoints, in healthy adults
title Impact of dietary supplementation with resistant dextrin (NUTRIOSE(®)) on satiety, glycaemia, and related endpoints, in healthy adults
title_full Impact of dietary supplementation with resistant dextrin (NUTRIOSE(®)) on satiety, glycaemia, and related endpoints, in healthy adults
title_fullStr Impact of dietary supplementation with resistant dextrin (NUTRIOSE(®)) on satiety, glycaemia, and related endpoints, in healthy adults
title_full_unstemmed Impact of dietary supplementation with resistant dextrin (NUTRIOSE(®)) on satiety, glycaemia, and related endpoints, in healthy adults
title_short Impact of dietary supplementation with resistant dextrin (NUTRIOSE(®)) on satiety, glycaemia, and related endpoints, in healthy adults
title_sort impact of dietary supplementation with resistant dextrin (nutriose(®)) on satiety, glycaemia, and related endpoints, in healthy adults
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572182/
https://www.ncbi.nlm.nih.gov/pubmed/34170392
http://dx.doi.org/10.1007/s00394-021-02618-9
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