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Efficacy of increased resistant starch consumption in human type 2 diabetes

Resistant starch (RS) has been shown to beneficially affect insulin sensitivity in healthy individuals and those with metabolic syndrome, but its effects on human type 2 diabetes (T2DM) are unknown. This study aimed to determine the effects of increased RS consumption on insulin sensitivity and gluc...

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Autores principales: Bodinham, C L, Smith, L, Thomas, E L, Bell, J D, Swann, J R, Costabile, A, Russell-Jones, D, Umpleby, A M, Robertson, M D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987287/
https://www.ncbi.nlm.nih.gov/pubmed/24671124
http://dx.doi.org/10.1530/EC-14-0036
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author Bodinham, C L
Smith, L
Thomas, E L
Bell, J D
Swann, J R
Costabile, A
Russell-Jones, D
Umpleby, A M
Robertson, M D
author_facet Bodinham, C L
Smith, L
Thomas, E L
Bell, J D
Swann, J R
Costabile, A
Russell-Jones, D
Umpleby, A M
Robertson, M D
author_sort Bodinham, C L
collection PubMed
description Resistant starch (RS) has been shown to beneficially affect insulin sensitivity in healthy individuals and those with metabolic syndrome, but its effects on human type 2 diabetes (T2DM) are unknown. This study aimed to determine the effects of increased RS consumption on insulin sensitivity and glucose control and changes in postprandial metabolites and body fat in T2DM. Seventeen individuals with well-controlled T2DM (HbA1c 46.6±2 mmol/mol) consumed, in a random order, either 40 g of type 2 RS (HAM-RS2) or a placebo, daily for 12 weeks with a 12-week washout period in between. At the end of each intervention period, participants attended for three metabolic investigations: a two-step euglycemic–hyperinsulinemic clamp combined with an infusion of [6,6-(2)H(2)] glucose, a meal tolerance test (MTT) with arterio-venous sampling across the forearm, and whole-body imaging. HAM-RS2 resulted in significantly lower postprandial glucose concentrations (P=0.045) and a trend for greater glucose uptake across the forearm muscle (P=0.077); however, there was no effect of HAM-RS2 on hepatic or peripheral insulin sensitivity, or on HbA1c. Fasting non-esterified fatty acid (NEFA) concentrations were significantly lower (P=0.004) and NEFA suppression was greater during the clamp with HAM-RS2 (P=0.001). Fasting triglyceride (TG) concentrations and soleus intramuscular TG concentrations were significantly higher following the consumption of HAM-RS2 (P=0.039 and P=0.027 respectively). Although fasting GLP1 concentrations were significantly lower following HAM-RS2 consumption (P=0.049), postprandial GLP1 excursions during the MTT were significantly greater (P=0.009). HAM-RS2 did not improve tissue insulin sensitivity in well-controlled T2DM, but demonstrated beneficial effects on meal handling, possibly due to higher postprandial GLP1.
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spelling pubmed-39872872014-04-17 Efficacy of increased resistant starch consumption in human type 2 diabetes Bodinham, C L Smith, L Thomas, E L Bell, J D Swann, J R Costabile, A Russell-Jones, D Umpleby, A M Robertson, M D Endocr Connect Research Resistant starch (RS) has been shown to beneficially affect insulin sensitivity in healthy individuals and those with metabolic syndrome, but its effects on human type 2 diabetes (T2DM) are unknown. This study aimed to determine the effects of increased RS consumption on insulin sensitivity and glucose control and changes in postprandial metabolites and body fat in T2DM. Seventeen individuals with well-controlled T2DM (HbA1c 46.6±2 mmol/mol) consumed, in a random order, either 40 g of type 2 RS (HAM-RS2) or a placebo, daily for 12 weeks with a 12-week washout period in between. At the end of each intervention period, participants attended for three metabolic investigations: a two-step euglycemic–hyperinsulinemic clamp combined with an infusion of [6,6-(2)H(2)] glucose, a meal tolerance test (MTT) with arterio-venous sampling across the forearm, and whole-body imaging. HAM-RS2 resulted in significantly lower postprandial glucose concentrations (P=0.045) and a trend for greater glucose uptake across the forearm muscle (P=0.077); however, there was no effect of HAM-RS2 on hepatic or peripheral insulin sensitivity, or on HbA1c. Fasting non-esterified fatty acid (NEFA) concentrations were significantly lower (P=0.004) and NEFA suppression was greater during the clamp with HAM-RS2 (P=0.001). Fasting triglyceride (TG) concentrations and soleus intramuscular TG concentrations were significantly higher following the consumption of HAM-RS2 (P=0.039 and P=0.027 respectively). Although fasting GLP1 concentrations were significantly lower following HAM-RS2 consumption (P=0.049), postprandial GLP1 excursions during the MTT were significantly greater (P=0.009). HAM-RS2 did not improve tissue insulin sensitivity in well-controlled T2DM, but demonstrated beneficial effects on meal handling, possibly due to higher postprandial GLP1. Bioscientifica Ltd 2014-04-15 /pmc/articles/PMC3987287/ /pubmed/24671124 http://dx.doi.org/10.1530/EC-14-0036 Text en © 2014 The authors http://creativecommons.org/licenses/by/3.0/deed.en_GB This work is licensed under a Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/deed.en_GB)
spellingShingle Research
Bodinham, C L
Smith, L
Thomas, E L
Bell, J D
Swann, J R
Costabile, A
Russell-Jones, D
Umpleby, A M
Robertson, M D
Efficacy of increased resistant starch consumption in human type 2 diabetes
title Efficacy of increased resistant starch consumption in human type 2 diabetes
title_full Efficacy of increased resistant starch consumption in human type 2 diabetes
title_fullStr Efficacy of increased resistant starch consumption in human type 2 diabetes
title_full_unstemmed Efficacy of increased resistant starch consumption in human type 2 diabetes
title_short Efficacy of increased resistant starch consumption in human type 2 diabetes
title_sort efficacy of increased resistant starch consumption in human type 2 diabetes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987287/
https://www.ncbi.nlm.nih.gov/pubmed/24671124
http://dx.doi.org/10.1530/EC-14-0036
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