A whole-grain diet reduces peripheral insulin resistance and improves glucose kinetics in obese adults: A randomized-controlled trial.

Steven K Malin, Emily L Kullman, Amanda R Scelsi, Jacob M Haus, Julianne Filion, Mangesh R Pagadala, Jean-Philippe Godin, Sunil Kochhar, Alastair B Ross, John P Kirwan
Author Information
  1. Steven K Malin: Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States.
  2. Emily L Kullman: Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States.
  3. Amanda R Scelsi: Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States.
  4. Jacob M Haus: Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States.
  5. Julianne Filion: Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States.
  6. Mangesh R Pagadala: Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States.
  7. Jean-Philippe Godin: Analytical Sciences Department, Nestlé Research Center, Lausanne, Switzerland.
  8. Sunil Kochhar: Analytical Sciences Department, Nestlé Research Center, Lausanne, Switzerland.
  9. Alastair B Ross: Analytical Sciences Department, Nestlé Research Center, Lausanne, Switzerland.
  10. John P Kirwan: Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States; Metabolic Research Center, Endocrinology and Metabolism Institute, Cleveland Clinic, Cleveland, OH, United States. Electronic address: kirwanj@ccf.org.

Abstract

BACKGROUND: Whole-grain intake is associated with lower risk of type 2 diabetes but the mechanisms are unclear.
PURPOSE: We tested the hypothesis that a WG diet reduces insulin resistance and improves glucose use in individuals at risk for type 2 diabetes compared with an isocaloric-matched refined-grain diet.
METHODS: A double-blind, randomized, controlled, crossover trial of 14 moderately obese adults (Age, 38 ± 2 y; BMI, 34.0 ± 1.1 kg/m). Insulin resistance and glucose metabolism was assessed using an oral glucose tolerance test combined with isotopic tracers of [6,6-H]-glucose and [U-C]-glucose, and indirect calorimetry. Peripheral and hepatic insulin resistance was assessed as 1/(rate of disposal/insulin), and endogenous glucose rates of appearance (R) iAUC × insulin iAUC, respectively. Both diets met ADA nutritional guidelines and contained either whole-grain (50 g per 1000 kcal) or equivalent refined-grain. All food was provided for 8 wk. with an 8-10 wk. washout period between diets.
RESULTS: Post-prandial glucose tolerance, peripheral insulin sensitivity, and metabolic flexibility (insulin-stimulated - fasting carbohydrate oxidation) improvements were greater after whole-grain compared to the refined-grain diet (P < 0.05). Compared to baseline, body fat (~2 kg) and hepatic R insulin resistance was reduced by both diets, while fasting glucose and exogenous glucose-meal were unchanged after both interventions. Changes in peripheral insulin resistance and metabolic flexibility correlated with improved glucose tolerance (P < 0.05).
CONCLUSION: Whole-grains reduced diabetes risk and the mechanisms appear to work through reduced post-prandial blood glucose and peripheral insulin resistance that were statistically linked to enhanced metabolic flexibility.

Keywords

Associated Data

ClinicalTrials.gov | NCT01411540

References

  1. Am J Clin Nutr. 2013 Jan;97(1):179-87 [PMID: 23235198]
  2. Gastroenterology. 2009 May;136(5):1552-60 [PMID: 19208352]
  3. J Appl Physiol (1985). 2013 Jul 1;115(1):78-83 [PMID: 23599396]
  4. J Nutr Metab. 2012;2012:462967 [PMID: 22363838]
  5. Am J Clin Nutr. 2003 Feb;77(2):385-91 [PMID: 12540398]
  6. Am J Clin Nutr. 2010 Jan;91(1):90-7 [PMID: 19889821]
  7. Obesity (Silver Spring). 2012 Jun;20(6):1313-8 [PMID: 22282048]
  8. Am J Clin Nutr. 2006 Feb;83(2):275-83 [PMID: 16469984]
  9. Am J Clin Nutr. 2005 Dec;82(6):1218-27 [PMID: 16332654]
  10. Med Sci Sports Exerc. 2001 Sep;33(9):1517-23 [PMID: 11528341]
  11. Nutr J. 2009 Sep 25;8:42 [PMID: 19781071]
  12. J Physiol. 1999 Mar 1;515 ( Pt 2):579-89 [PMID: 10050023]
  13. Obesity (Silver Spring). 2008 Feb;16(2):298-305 [PMID: 18239636]
  14. J Nutr. 2010 Nov;140(11):1932-6 [PMID: 20810606]
  15. Arch Intern Med. 2010 Jun 14;170(11):961-9 [PMID: 20548009]
  16. J Nutr. 2012 Apr;142(4):710-6 [PMID: 22357746]
  17. J Nutr. 2012 Jul;142(7):1304-13 [PMID: 22649266]
  18. Br J Nutr. 2010 Jul;104(1):125-34 [PMID: 20307353]
  19. Am J Clin Nutr. 2008 Jan;87(1):79-90 [PMID: 18175740]
  20. J Nutr. 2007 Jun;137(6):1401-7 [PMID: 17513398]
  21. Am J Clin Nutr. 2002 May;75(5):848-55 [PMID: 11976158]
  22. Am J Clin Nutr. 2012 Nov;96(5):1017-24 [PMID: 22990033]
  23. J Appl Physiol Respir Environ Exerc Physiol. 1983 Aug;55(2):628-34 [PMID: 6618956]
  24. Anal Biochem. 2009 Feb 1;385(1):7-12 [PMID: 19010298]
  25. Am J Clin Nutr. 2003 Nov;78(5):965-71 [PMID: 14594783]
  26. Am J Clin Nutr. 2005 Sep;82(3):559-67 [PMID: 16155268]
  27. Endocr Pract. 2016 Jul;22 Suppl 3:1-203 [PMID: 27219496]
  28. Am J Physiol Endocrinol Metab. 2013 Nov 15;305(10):E1292-8 [PMID: 24064339]
  29. Diabetes. 2009 Jul;58(7):1509-17 [PMID: 19366864]
  30. Br J Nutr. 2007 Nov;98(5):929-36 [PMID: 17562226]
  31. Am J Clin Nutr. 2014 Aug;100(2):577-86 [PMID: 24944054]
  32. Metabolism. 1993 Jun;42(6):780-5 [PMID: 8510524]
  33. J Nutr. 2016 Nov;146(11):2244-2251 [PMID: 27798329]
  34. Diabetologia. 2010 May;53(5):858-65 [PMID: 20182862]
  35. Am J Clin Nutr. 2003 Apr;77(4):967-74 [PMID: 12663299]
  36. J Nutr. 2015 Feb;145(2):199-206 [PMID: 25644338]
  37. Diabetes. 2000 May;49(5):677-83 [PMID: 10905472]

Grants

  1. P30 DK020572/NIDDK NIH HHS
  2. T32 DK007319/NIDDK NIH HHS
  3. UL1 RR024989/NCRR NIH HHS
  4. UL1 TR000439/NCATS NIH HHS

MeSH Term

Adult
Blood Glucose
Cross-Over Studies
Dietary Fiber
Double-Blind Method
Female
Glucose
Humans
Insulin Resistance
Male
Obesity
Treatment Outcome
Whole Grains

Chemicals

Blood Glucose
Dietary Fiber
Glucose

Word Cloud

Created with Highcharts 10.0.0glucoseinsulinresistancediettoleranceperipheralriskdiabetesrefined-graindietswhole-grainmetabolicflexibilityreducedtype2mechanismsreducesimprovescomparedtrialobeseInsulinassessedhepaticRfastingP < 005BACKGROUND:Whole-grainintakeassociatedlowerunclearPURPOSE:testedhypothesisWGuseindividualsisocaloric-matchedMETHODS:double-blindrandomizedcontrolledcrossover14moderatelyadultsAge38 ± 2 yBMI340 ± 11 kg/mmetabolismusingoraltestcombinedisotopictracers[66-H]-glucose[U-C]-glucoseindirectcalorimetryPeripheral1/ratedisposal/insulinendogenousratesappearanceiAUC × insuliniAUCrespectivelymetADAnutritionalguidelinescontainedeither50 gper1000 kcalequivalentfoodprovided8 wk8-10 wkwashoutperiodRESULTS:Post-prandialsensitivityinsulin-stimulated-carbohydrateoxidationimprovementsgreaterComparedbaselinebodyfat~2 kgexogenousglucose-mealunchangedinterventionsChangescorrelatedimprovedCONCLUSION:Whole-grainsappearworkpost-prandialbloodstatisticallylinkedenhancedkineticsadults:randomized-controlledAlkylresorcinolsGlucoseLow-glycemicObesity

Similar Articles

Cited By