Fasting and diurnal blood ketonemia and glycemia responses to a six-week, energy-controlled ketogenic diet, supplemented with racemic R/S-BHB salts.


Journal

Clinical nutrition ESPEN
ISSN: 2405-4577
Titre abrégé: Clin Nutr ESPEN
Pays: England
ID NLM: 101654592

Informations de publication

Date de publication:
04 2023
Historique:
received: 28 11 2022
revised: 20 01 2023
accepted: 25 01 2023
medline: 28 3 2023
entrez: 24 3 2023
pubmed: 25 3 2023
Statut: ppublish

Résumé

Single doses of exogenous ketone salts (KS) transiently increase circulating beta-hydroxybutyrate (BHB) (∼1 mM; 1-2 h) regardless of starting levels of ketosis; however, no studies have explored how sustained use of KS influences measures of ketonemia and glycemia. To determine the response to a hypocaloric, well-formulated ketogenic diet (KD), with and without the inclusion of two daily racemic KS doses (6 g R-BHB + 6 g S-BHB per serving) on 1) daily fasting capillary R-BHB and glucose (R-BHB/GLU Non-diabetic adults with overweight and obesity were randomized to receive a precisely measured hypocaloric KD (∼75 %en of maintenance) for six weeks, supplemented twice-daily with KS or placebo (PL). A non-randomized comparison group was provided an isonitrogenous/isoenergetic low-fat diet (LFD). All meals were provided to subjects. Capillary blood was collected daily to measure R-BHB/GLU Mean R-BHB A hypocaloric KD was effective at reducing diurnal glucose compared to a LFD independent of weight loss, but twice-daily racemic KS ingestion during KD augmented ketonemia, both as R- and S-BHB, and decreased mean fasting glucose beyond a KD alone. The hypoglycemic effects of KD in combination with exogenous ketones merit further investigation.

Sections du résumé

BACKGROUND
Single doses of exogenous ketone salts (KS) transiently increase circulating beta-hydroxybutyrate (BHB) (∼1 mM; 1-2 h) regardless of starting levels of ketosis; however, no studies have explored how sustained use of KS influences measures of ketonemia and glycemia.
OBJECTIVES
To determine the response to a hypocaloric, well-formulated ketogenic diet (KD), with and without the inclusion of two daily racemic KS doses (6 g R-BHB + 6 g S-BHB per serving) on 1) daily fasting capillary R-BHB and glucose (R-BHB/GLU
METHODS
Non-diabetic adults with overweight and obesity were randomized to receive a precisely measured hypocaloric KD (∼75 %en of maintenance) for six weeks, supplemented twice-daily with KS or placebo (PL). A non-randomized comparison group was provided an isonitrogenous/isoenergetic low-fat diet (LFD). All meals were provided to subjects. Capillary blood was collected daily to measure R-BHB/GLU
RESULTS
Mean R-BHB
CONCLUSIONS
A hypocaloric KD was effective at reducing diurnal glucose compared to a LFD independent of weight loss, but twice-daily racemic KS ingestion during KD augmented ketonemia, both as R- and S-BHB, and decreased mean fasting glucose beyond a KD alone. The hypoglycemic effects of KD in combination with exogenous ketones merit further investigation.

Identifiants

pubmed: 36963874
pii: S2405-4577(23)00032-3
doi: 10.1016/j.clnesp.2023.01.030
pii:
doi:

Substances chimiques

3-Hydroxybutyric Acid TZP1275679
Salts 0
Ketone Bodies 0
Ketones 0
Glucose IY9XDZ35W2
Insulin 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

277-287

Informations de copyright

Copyright © 2023 European Society for Clinical Nutrition and Metabolism. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest JV receives royalties for low-carbohydrate nutrition books; is founder, consultant, and stockholder of Virta Health, Inc. and is a member of the advisory boards for Simply Good Foods. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Alex Buga (A)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA.

Madison L Kackley (ML)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA.

Christopher D Crabtree (CD)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA.

Teryn N Bedell (TN)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA.

Bradley T Robinson (BT)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA.

Justen T Stoner (JT)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA.

Drew D Decker (DD)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA.

Parker N Hyde (PN)

Department of Kinesiology, University of Northern Georgia, Dahlonega, GA 30597, USA.

Rich A LaFountain (RA)

Big Sky Health, Big Sky, MT 59716, USA.

Milene L Brownlow (ML)

National Institute of Environmental Health Sciences, Durham, NC 27709, USA.

Annalouise O'Connor (A)

Danone, Inc., Broomfield, CO 80021, USA.

Deepa Krishnan (D)

College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.

Craig A McElroy (CA)

College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.

William J Kraemer (WJ)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA.

Jeff S Volek (JS)

Department of Human Sciences, The Ohio State University, Columbus, OH 43210, USA. Electronic address: volek.1@osu.edu.

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Classifications MeSH