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A Whole-Grain Diet Increases Glucose-Stimulated Insulin Secretion Independent of Gut Hormones in Adults at Risk for Type 2 Diabetes.

Authors :
Malin SK
Kullman EL
Scelsi AR
Godin JP
Ross AB
Kirwan JP
Source :
Molecular nutrition & food research [Mol Nutr Food Res] 2019 Apr; Vol. 63 (7), pp. e1800967. Date of Electronic Publication: 2019 Mar 20.
Publication Year :
2019

Abstract

Introduction: The effect of whole-grain (WG) versus refined-grain (RG) diets on glucose-stimulated insulin secretion (GSIS) and β-cell function is unclear.<br />Methods: In a double-blind crossover randomized controlled trial, 13 prediabetic adults (37.2 ± 1.8 y, BMI: 33.6 ± 1.4 kg m <superscript>-2</superscript> , 2 h glucose: 146.9 ± 11.6 mg dL <superscript>-1</superscript> ) are provided isocaloric-matched WG and RG diets for 8-weeks each, with an 8-10 week washout between diets. Glucose, insulin, and C-peptide are studied over 240 min following a 75 g OGTT. Incretins (GLP-1 and GIP), PYY, and total ghrelin are assessed at 0, 30, and 60 min. Mixed-meal diets for carbohydrate (54%), fat (28%), and protein (18%) contain either WG (50 g/1000 kcal) or equivalent RG.<br />Results: Both diets induce fat loss (≈2 kg). While neither diet impacts early phase GSIS, the WG diet increases total GSIS (iAUC of C-peptide <subscript>0-240</subscript> /Glc <subscript>0-240</subscript> , p = 0.02) and β-cell function (disposition index; GSIS × insulin sensitivity, p = 0.02). GIP and PYY are unaltered by either diet, but GLP-1 is higher at 30 min following RG versus WG (p = 0.04). Ghrelin levels are higher at 60 min of the OGTT following both interventions (p = 0.01).<br />Conclusion: A WG-rich diet increases β-cell function independent of gut hormones in adults with prediabetes.<br /> (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1613-4133
Volume :
63
Issue :
7
Database :
MEDLINE
Journal :
Molecular nutrition & food research
Publication Type :
Academic Journal
Accession number :
30763457
Full Text :
https://doi.org/10.1002/mnfr.201800967