A wheat aleurone-rich diet improves oxidative stress but does not influence glucose metabolism in overweight/obese individuals: Results from a randomized controlled trial.


Journal

Nutrition, metabolism, and cardiovascular diseases : NMCD
ISSN: 1590-3729
Titre abrégé: Nutr Metab Cardiovasc Dis
Pays: Netherlands
ID NLM: 9111474

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 15 09 2021
revised: 16 12 2021
accepted: 17 12 2021
pubmed: 7 2 2022
medline: 11 3 2022
entrez: 6 2 2022
Statut: ppublish

Résumé

Aleurone is the innermost layer of wheat bran, rich in fiber, minerals, vitamins, phenolic compounds, and betaine. The metabolic effects of aleurone rich foods are still unknown. Our aim was to investigate the effects of consuming a Wheat Aleurone rich diet vs. a Refined Wheat diet for 8 weeks on fasting and postprandial glycemic and lipid metabolism, inflammation, and oxidative stress in overweight/obese individuals. According to a randomized cross-over study design, 23 overweight/obese individuals, age 56 ± 9 years (M±SD), were assigned to two isoenergetic diet - Wheat Aleurone and Refined Wheat diets - for 8 weeks. The diets were similar for macronutrient composition but different for the aleurone content (40-50 g/day in the Wheat Aleurone diet). After each diet, fasting and postprandial plasma metabolic profile, ferulic acid metabolites and 8-isoprostane concentrations in 24-h urine samples were evaluated. Compared with the Refined Wheat Diet, the Wheat Aleurone Diet increased fasting plasma concentrations of betaine by 15% (p = 0.042) and decreased the excretion of 8-isoprostane by 33% (p = 0.035). Conversely, it did not affect the fasting and postprandial glucose, insulin and triglyceride responses, homocysteine, and C-Reactive Protein concentrations, nor excretion of phenolic metabolites. An 8-week Wheat Aleurone Diet improves the oxidative stress and increases plasma betaine levels in overweight/obese individuals with an increased cardiometabolic risk. However, further studies with longer duration and larger sample size are needed to evaluate the benefits of aleurone-rich foods on glucose and lipid metabolism in individuals with more severe metabolic abnormalities. NCT02150356, (https://clinicaltrials.gov).

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Aleurone is the innermost layer of wheat bran, rich in fiber, minerals, vitamins, phenolic compounds, and betaine. The metabolic effects of aleurone rich foods are still unknown. Our aim was to investigate the effects of consuming a Wheat Aleurone rich diet vs. a Refined Wheat diet for 8 weeks on fasting and postprandial glycemic and lipid metabolism, inflammation, and oxidative stress in overweight/obese individuals.
METHODS AND RESULTS RESULTS
According to a randomized cross-over study design, 23 overweight/obese individuals, age 56 ± 9 years (M±SD), were assigned to two isoenergetic diet - Wheat Aleurone and Refined Wheat diets - for 8 weeks. The diets were similar for macronutrient composition but different for the aleurone content (40-50 g/day in the Wheat Aleurone diet). After each diet, fasting and postprandial plasma metabolic profile, ferulic acid metabolites and 8-isoprostane concentrations in 24-h urine samples were evaluated. Compared with the Refined Wheat Diet, the Wheat Aleurone Diet increased fasting plasma concentrations of betaine by 15% (p = 0.042) and decreased the excretion of 8-isoprostane by 33% (p = 0.035). Conversely, it did not affect the fasting and postprandial glucose, insulin and triglyceride responses, homocysteine, and C-Reactive Protein concentrations, nor excretion of phenolic metabolites.
CONCLUSION CONCLUSIONS
An 8-week Wheat Aleurone Diet improves the oxidative stress and increases plasma betaine levels in overweight/obese individuals with an increased cardiometabolic risk. However, further studies with longer duration and larger sample size are needed to evaluate the benefits of aleurone-rich foods on glucose and lipid metabolism in individuals with more severe metabolic abnormalities.
CLINICAL TRIAL REGISTRY NUMBER BACKGROUND
NCT02150356, (https://clinicaltrials.gov).

Identifiants

pubmed: 35123855
pii: S0939-4753(21)00594-9
doi: 10.1016/j.numecd.2021.12.016
pii:
doi:

Substances chimiques

Blood Glucose 0
Dietary Fiber 0
Plant Proteins 0
aleurone 0

Banques de données

ClinicalTrials.gov
['NCT02150356']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

715-726

Informations de copyright

Copyright © 2021 The Italian Diabetes Society, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Gabriele Riccardi is member of the Health and Wellbeing Advisory Board of the Barilla company; remuneration for this activity goes to his University Department. All other authors declare no conflict of interest.

Auteurs

Giuseppina Costabile (G)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy. Electronic address: giuseppina.costabile@unina.it.

Marilena Vitale (M)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy.

Giuseppe Della Pepa (G)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy.

Paola Cipriano (P)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy.

Claudia Vetrani (C)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy.

Roberta Testa (R)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy.

Pedro Mena (P)

Human Nutrition Unit, Department of Food and Drug, University of Parma, Via Volturno, 39, 43125, Parma, Italy.

Letizia Bresciani (L)

Human Nutrition Unit, Department of Food and Drug, University of Parma, Via Volturno, 39, 43125, Parma, Italy.

Michele Tassotti (M)

Human Nutrition Unit, Department of Food and Drug, University of Parma, Via Volturno, 39, 43125, Parma, Italy.

Luca Calani (L)

Human Nutrition Unit, Department of Food and Drug, University of Parma, Via Volturno, 39, 43125, Parma, Italy.

Daniele Del Rio (D)

Human Nutrition Unit, Department of Food and Drug, University of Parma, Via Volturno, 39, 43125, Parma, Italy.

Furio Brighenti (F)

Human Nutrition Unit, Department of Food and Drug, University of Parma, Via Volturno, 39, 43125, Parma, Italy.

Raffaele Napoli (R)

Department of Translational Medical Sciences, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy.

Angela A Rivellese (AA)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy.

Gabriele Riccardi (G)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini, 5, 80131 Naples, Italy.

Rosalba Giacco (R)

Institute of Food Sciences, National Research Council, Via Roma 64, 8 Avellino, Italy.

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Classifications MeSH