Dietary carbohydrate restriction improves metabolic syndrome independent of weight loss.


Journal

JCI insight
ISSN: 2379-3708
Titre abrégé: JCI Insight
Pays: United States
ID NLM: 101676073

Informations de publication

Date de publication:
20 06 2019
Historique:
received: 20 02 2019
accepted: 01 05 2019
entrez: 21 6 2019
pubmed: 21 6 2019
medline: 25 8 2020
Statut: epublish

Résumé

BACKGROUNDMetabolic syndrome (MetS) is highly correlated with obesity and cardiovascular risk, but the importance of dietary carbohydrate independent of weight loss in MetS treatment remains controversial. Here, we test the theory that dietary carbohydrate intolerance (i.e., the inability to process carbohydrate in a healthy manner) rather than obesity per se is a fundamental feature of MetS.METHODSIndividuals who were obese with a diagnosis of MetS were fed three 4-week weight-maintenance diets that were low, moderate, and high in carbohydrate. Protein was constant and fat was exchanged isocalorically for carbohydrate across all diets.RESULTSDespite maintaining body mass, low-carbohydrate (LC) intake enhanced fat oxidation and was more effective in reversing MetS, especially high triglycerides, low HDL-C, and the small LDL subclass phenotype. Carbohydrate restriction also improved abnormal fatty acid composition, an emerging MetS feature. Despite containing 2.5 times more saturated fat than the high-carbohydrate diet, an LC diet decreased plasma total saturated fat and palmitoleate and increased arachidonate.CONCLUSIONConsistent with the perspective that MetS is a pathologic state that manifests as dietary carbohydrate intolerance, these results show that compared with eucaloric high-carbohydrate intake, LC/high-fat diets benefit MetS independent of whole-body or fat mass.TRIAL REGISTRATIONClinicalTrials.gov Identifier: NCT02918422.FUNDINGDairy Management Inc. and the Dutch Dairy Association.

Identifiants

pubmed: 31217353
pii: 128308
doi: 10.1172/jci.insight.128308
pmc: PMC6629108
doi:
pii:

Substances chimiques

Cholesterol, LDL 0
Dietary Carbohydrates 0
Arachidonic Acid 27YG812J1I
8,11,14-Eicosatrienoic Acid FC398RK06S

Banques de données

ClinicalTrials.gov
['NCT02918422']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Parker N Hyde (PN)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Teryn N Sapper (TN)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Christopher D Crabtree (CD)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Richard A LaFountain (RA)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Madison L Bowling (ML)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Alex Buga (A)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Brandon Fell (B)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Fionn T McSwiney (FT)

Department of Sport and Exercise Science, Waterford Institute of Technology, Waterford, Ireland.

Ryan M Dickerson (RM)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Vincent J Miller (VJ)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Debbie Scandling (D)

Davis Heart & Lung Research Institute, Department of Radiology; Department of Internal Medicine, Division of Cardiovascular Medicine; Wexner Medical Center, The Ohio State University, Columbus, Ohio, USA.

Orlando P Simonetti (OP)

Davis Heart & Lung Research Institute, Department of Radiology; Department of Internal Medicine, Division of Cardiovascular Medicine; Wexner Medical Center, The Ohio State University, Columbus, Ohio, USA.

Stephen D Phinney (SD)

Virta Health, San Francisco, California, USA.

William J Kraemer (WJ)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

Sarah A King (SA)

Department of Atherosclerosis Research, Children's Hospital Oakland Research Institute, Oakland, California, USA.

Ronald M Krauss (RM)

Department of Atherosclerosis Research, Children's Hospital Oakland Research Institute, Oakland, California, USA.

Jeff S Volek (JS)

Department of Human Sciences, The Ohio State University, Columbus, Ohio, USA.

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Classifications MeSH