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Effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial

OBJECTIVE: Large preloads of protein and fat have been shown to lower glucose after a carbohydrate-rich meal in people with type 2 diabetes but add a considerable energy burden. Low calorie preloads [<5% of daily energy intake] have been tested in this study in people with prediabetes and with ty...

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Autores principales: Clifton, Peter M, Galbraith, Claire, Coles, Leah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216833/
https://www.ncbi.nlm.nih.gov/pubmed/25343850
http://dx.doi.org/10.1186/1475-2891-13-103
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author Clifton, Peter M
Galbraith, Claire
Coles, Leah
author_facet Clifton, Peter M
Galbraith, Claire
Coles, Leah
author_sort Clifton, Peter M
collection PubMed
description OBJECTIVE: Large preloads of protein and fat have been shown to lower glucose after a carbohydrate-rich meal in people with type 2 diabetes but add a considerable energy burden. Low calorie preloads [<5% of daily energy intake] have been tested in this study in people with prediabetes and with type 2 diabetes. RESEARCH DESIGN AND METHODS: This was an unblinded randomised crossover study with two placebo days and two active treatment days. Glucose was measured for 3 hours with fingerprick samples as well as continuous glucose monitoring [CGMS]. Twenty-four subjects with pre-diabetes or moderately controlled type 2 diabetes [fasting glucose < 10 and HbA1c < 8.5%] were recruited. The preload contained 17 g whey protein plus 3 g lactose and 5 g guar, and 1 g flavour material [including sucralose] dissolved in 150 ml cold water or 150 ml cold water with no additives. The breakfast test meal consisted of 2 slices of bread, margarine and jam [3 slices for men] with the test drink 15 minutes beforehand. RESULTS: Peak fingerprick glucose was reduced by 2.1 mmol/L at 45 min [p < 0.0001]. Average fingerprick glucose over 3 hours was reduced by 0.8 mmol/L [p = 0.0003]. There was no difference between those with diabetes or prediabetes or those on medication or not on medication. CONCLUSIONS: An 80 kcal whey protein/fibre preload can lower average glucose over 3 hours by 0.8 mmol/L. If used long term before at least two carbohydrate-rich meals/day this preload could lower HbA1c by up to 1%. TRIAL REGISTRATION: The trial was registered with the Australian New Zealand Clinical Trials Registry number ACTRN12612001251819.
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spelling pubmed-42168332014-11-04 Effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial Clifton, Peter M Galbraith, Claire Coles, Leah Nutr J Research OBJECTIVE: Large preloads of protein and fat have been shown to lower glucose after a carbohydrate-rich meal in people with type 2 diabetes but add a considerable energy burden. Low calorie preloads [<5% of daily energy intake] have been tested in this study in people with prediabetes and with type 2 diabetes. RESEARCH DESIGN AND METHODS: This was an unblinded randomised crossover study with two placebo days and two active treatment days. Glucose was measured for 3 hours with fingerprick samples as well as continuous glucose monitoring [CGMS]. Twenty-four subjects with pre-diabetes or moderately controlled type 2 diabetes [fasting glucose < 10 and HbA1c < 8.5%] were recruited. The preload contained 17 g whey protein plus 3 g lactose and 5 g guar, and 1 g flavour material [including sucralose] dissolved in 150 ml cold water or 150 ml cold water with no additives. The breakfast test meal consisted of 2 slices of bread, margarine and jam [3 slices for men] with the test drink 15 minutes beforehand. RESULTS: Peak fingerprick glucose was reduced by 2.1 mmol/L at 45 min [p < 0.0001]. Average fingerprick glucose over 3 hours was reduced by 0.8 mmol/L [p = 0.0003]. There was no difference between those with diabetes or prediabetes or those on medication or not on medication. CONCLUSIONS: An 80 kcal whey protein/fibre preload can lower average glucose over 3 hours by 0.8 mmol/L. If used long term before at least two carbohydrate-rich meals/day this preload could lower HbA1c by up to 1%. TRIAL REGISTRATION: The trial was registered with the Australian New Zealand Clinical Trials Registry number ACTRN12612001251819. BioMed Central 2014-10-25 /pmc/articles/PMC4216833/ /pubmed/25343850 http://dx.doi.org/10.1186/1475-2891-13-103 Text en © Clifton et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Clifton, Peter M
Galbraith, Claire
Coles, Leah
Effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial
title Effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial
title_full Effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial
title_fullStr Effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial
title_full_unstemmed Effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial
title_short Effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial
title_sort effect of a low dose whey/guar preload on glycemic control in people with type 2 diabetes-a randomised controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216833/
https://www.ncbi.nlm.nih.gov/pubmed/25343850
http://dx.doi.org/10.1186/1475-2891-13-103
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