Mechanisms underlying the cardiometabolic protective effect of walnut consumption in obese people: A cross-over, randomized, double-blind, controlled inpatient physiology study.


Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
09 2019
Historique:
received: 12 03 2019
revised: 05 05 2019
accepted: 09 05 2019
pubmed: 16 5 2019
medline: 14 7 2020
entrez: 16 5 2019
Statut: ppublish

Résumé

To assess the effects of walnuts on cardiometabolic outcomes in obese people and to explore the underlying mechanisms using novel methods including metabolomic, lipidomic, glycomic and microbiome analysis, integrated with lipid particle fractionation, appetite-regulating hormones and haemodynamic measurements. A total of 10 obese individuals were enrolled in this cross-over, randomized, double-blind, placebo-controlled clinical trial. The participants had two 5-day inpatient stays, during which they consumed a smoothie containing 48 g walnuts or a macronutrient-matched placebo smoothie without nuts, with a 1-month washout period between the two visits. Walnut consumption improved aspects of the lipid profile; it reduced fasting small and dense LDL particles (P < 0.02) and increased postprandial large HDL particles (P < 0.01). Lipoprotein insulin resistance score, glucose and the insulin area under the curve (AUC) decreased significantly after walnut consumption (P < 0.01, P < 0.02 and P < 0.04, respectively). Consuming walnuts significantly increased 10 N-glycans, with eight of them carrying a fucose core. Lipidomic analysis showed a robust reduction in harmful ceramides, hexosylceramides and sphingomyelins, which have been shown to mediate effects on cardiometabolic risk. The peptide YY AUC significantly increased after walnut consumption (P < 0.03). No major significant changes in haemodynamic or metabolomic analysis or in microbiome host health-promoting bacteria such as Faecalibacterium were found. These data provide a more comprehensive mechanistic perspective of the effect of dietary walnut consumption on cardiometabolic variables. Lipidomic and lipid nuclear magnetic resonance spectroscopy analysis showed an early but significant reduction in ceramides and other atherogenic lipids with walnut consumption, which may explain the longer-term benefits of walnuts or other nuts on insulin resistance, cardiovascular risk and mortality.

Identifiants

pubmed: 31087608
doi: 10.1111/dom.13773
pmc: PMC6684390
mid: NIHMS1040757
doi:

Substances chimiques

Lipids 0
Peptide YY 106388-42-5

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2086-2095

Subventions

Organisme : NIDDK NIH HHS
ID : K24 DK081913
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR025758
Pays : United States

Informations de copyright

Published 2019. This article is a U.S. Government work and is in the public domain in the USA.

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Auteurs

Dario Tuccinardi (D)

Division of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.
Unit of Endocrinology and Diabetes, Department of Medicine, Campus Bio-Medico University of Rome, Rome, Italy.

Olivia M Farr (OM)

Division of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.

Jagriti Upadhyay (J)

Division of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.

Sabrina M Oussaada (SM)

Division of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.

Maria I Klapa (MI)

Department of Chemical & Biomolecular Engineering & Bioengineering, Metabolic Engineering and Systems Biology Laboratory, Institute of Chemical Engineering Sciences, Foundation for Research and Technology-Hellas, Patras, Greece.

Marco Candela (M)

Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.

Simone Rampelli (S)

Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.

Sylvain Lehoux (S)

Department of Surgery, Beth Israel Deaconess Medical Centre, Harvard Medical School, Boston, Massachusetts.
Department of Surgery, Beth Israel Deaconess Medical Centre Glycomics Core, Boston, Massachusetts.

Iolanda Lázaro (I)

CIBERde Fisiopatología de la Obesidad y la Nutrición (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain.
Lipid Clinic, Department of Endocrinology and Nutrition, Institut d'Investigacions Biomediques August PiSunyer (IDIBAPS), Hospital Clinic, University of Barcelona, Barcelona, Spain.

Aleix Sala-Vila (A)

CIBERde Fisiopatología de la Obesidad y la Nutrición (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain.
Lipid Clinic, Department of Endocrinology and Nutrition, Institut d'Investigacions Biomediques August PiSunyer (IDIBAPS), Hospital Clinic, University of Barcelona, Barcelona, Spain.

Patrizia Brigidi (P)

Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.

Richard D Cummings (RD)

Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.

Christos S Mantzoros (CS)

Division of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.
Section of Endocrinology, Department of Medicine, VA Boston Healthcare System, Boston, Massachusetts.

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