An extra virgin olive oil-enriched chocolate spread positively modulates insulin-resistance markers compared with a palm oil-enriched one in healthy young adults: A double-blind, cross-over, randomised controlled trial.


Journal

Diabetes/metabolism research and reviews
ISSN: 1520-7560
Titre abrégé: Diabetes Metab Res Rev
Pays: England
ID NLM: 100883450

Informations de publication

Date de publication:
02 2022
Historique:
revised: 19 07 2021
received: 11 06 2021
accepted: 16 08 2021
pubmed: 27 8 2021
medline: 1 4 2022
entrez: 26 8 2021
Statut: ppublish

Résumé

To investigate if extra virgin olive oil (EVOO) or palm oil enriched chocolate spreads consumption leads to different results in terms of plasma ceramides concentration, glucose and lipid metabolism, inflammatory markers and appetite regulation in young healthy subjects. In a 2-week, double-blind, cross-over, randomised controlled trial, 20 healthy, normal-weight subjects with a mean age of 24.2 years (SD: 1.2), consumed chocolate spread snacks (73% of energy [%E] from fat, 20% from carbohydrates and 7% from proteins), providing 570 Kcal/day added to an isocaloric diet. The chocolate spreads were identical, except for the type of fat: EVOO oil, rich in monounsaturated fatty acids (MUFAs), or palm oil, rich in Saturated Fatty Acids (SFAs). EVOO-enriched chocolate spread consumption led to better circulating sphingolipids and glucose profile, with reduced plasma ceramide C16:0, ceramide C16:0/ceramide C22:0-ceramide C24:0 ratio and sphingomyelin C18:0 (P = 0.030, P= 0.032 and P = 0.042, respectively) compared to the palm oil-enriched chocolate spread diet. HOMA-IR and plasma insulin were lower, while the Quicki and the McAuley Index were higher after the EVOO diet compared to the palm oil diet (P = 0.046, P = 0.045, P = 0.018 and P = 0.039 respectively). Subjects maintained a stable weight throughout the study. No major significant changes in total cholesterol, triglycerides, HDL, inflammatory markers, and appetite-regulating hormones/visual analogue scale were observed between the groups. Partially replacing SFAs with MUFAs in a chocolate-based snack as part of a short-term isocaloric diet in healthy individuals may limit SFAs detrimental effects on insulin sensitivity and decrease circulating harmful sphingolipids in young adults.

Identifiants

pubmed: 34435429
doi: 10.1002/dmrr.3492
pmc: PMC9286378
doi:

Substances chimiques

Insulins 0
Olive Oil 0
Palm Oil 5QUO05548Z

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e3492

Informations de copyright

© 2021 VENCHI SpA. Diabetes/Metabolism Research and Reviews published by John Wiley & Sons Ltd.

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Auteurs

Dario Tuccinardi (D)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Antonio Di Mauro (A)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Greta Lattanzi (G)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Giovanni Rossini (G)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Lavinia Monte (L)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Ivan Beato (I)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Chiara Spiezia (C)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Maria Bravo (M)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Mikiko Watanabe (M)

Department of Experimental Medicine, Section of Medical Pathophysiology, Food Science and Endocrinology, Sapienza University of Rome, Rome, Italy.

Andreea Soare (A)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Shadi Kyanvash (S)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Andrea Armirotti (A)

Analytical Chemistry Lab, Fondazione Istituto Italiano di Tecnologia, Genova, Italy.

Sine Mandrup Bertozzi (SM)

Analytical Chemistry Lab, Fondazione Istituto Italiano di Tecnologia, Genova, Italy.

Amalia Gastaldelli (A)

Institute of Clinical Physiology, National Research Council, Pisa, Italy.

Claudio Pedone (C)

Department of Medicine, Unit of Geriatrics, Biomedical Campus of Rome, Rome, Italy.

Yeganeh Manon Khazrai (YM)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

Paolo Pozzilli (P)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.
Centre of Immunobiology, Barts and London School of Medicine and Dentistry, Queen Mary University of London, London, UK.

Silvia Manfrini (S)

Department of Medicine, Unit of Endocrinology and Diabetes, Campus Bio-Medico of Rome, Rome, Italy.

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Classifications MeSH