Evidence map›Paper›PMID 31599919›Full record

Trial reportThe American journal of clinical nutrition2019

A ketone monoester drink reduces the glycemic response to an oral glucose challenge in individuals with obesity: a randomized trial.

Étienne Myette-Côté, Hannah G Caldwell, Philip N Ainslie, Kieran Clarke, Jonathan P Little

2 registry-linked trialsOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The American journal of clinical nutrition, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
5.1field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03461068 phase1completednot on this map

The Effect of Exogenous Ketone Monoester Supplement on Glycemic Response to an Oral Glucose Tolerance Test

TypeinterventionalSponsorUniversity of British ColumbiaRan2018 to 2018Enrolled15ConditionsKetones, Dietary SupplementsArmsKetone monoester, Placebo
NCT07364162 phase2recruitingnot on this mapstarted 2026, after this paper: background citation

Exogenous Ketone Ester Supplementation in ICU Delirium (KETONES ICU)

TypeinterventionalSponsorVanderbilt University Medical CenterRan2026 to 2027Enrolled40ConditionsICU Delirium, Critical IllnessArmsKetone monoester, Placebo
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 87 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Étienne Myette-CôtéSchool of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, British Columbia, Canada.
Hannah G CaldwellSchool of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, British Columbia, Canada.
Philip N AinslieSchool of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, British Columbia, Canada.
Kieran ClarkeDepartment of Physiology, Anatomy, and Genetics, University of Oxford, Oxford, United Kingdom.
Jonathan P LittleSchool of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, British Columbia, Canada.
University of British Columbia · CAUniversity of Oxford · GB

Funding

CIHR MSH-141980
6 · The paper itself

Abstract

backgroundExogenous ketones make it possible to reach a state of ketosis that may improve metabolic control in humans.

objectivesThe main objective of this study was to determine whether the ingestion of a ketone monoester (KE) drink before a 2-h oral-glucose-tolerance test (OGTT) would lower blood glucose concentrations. Secondary objectives were to determine the impact of KE on nonesterified fatty acid (NEFA) concentration and glucoregulatory hormones.

methodsWe conducted a randomized controlled crossover experiment in 15 individuals with obesity (mean ± SD age: 47 ± 10 y; BMI: 34 ± 5 kg/m2). After an overnight fast, participants consumed a KE drink [(R)-3-hydroxybutyl (R)-3-hydroxybutyrate; 0.45 mL/kg body weight] or taste-matched control drink 30 min before completing a 75-g OGTT. Participants and study personnel performing laboratory analyses were blinded to each condition.

resultsThe KE increased d-β-hydroxybutyrate to a maximum of ∼3.4 mM (P < 0.001) during the OGTT. Compared with the control drink, KE reduced glucose (-11%, P = 0.002), NEFA (-21%, P = 0.009), and glucagon-like peptide 1 (-31%, P = 0.001) areas under the curve (AUCs), whereas glucagon AUC increased (+11%, P = 0.030). No differences in triglyceride, C-peptide, and insulin AUCs were observed after the KE drink. Mean arterial blood pressure decreased and heart rate increased after the KE drink (both P < 0.01).

conclusionsA KE drink consumed before an OGTT lowered glucose and NEFA AUCs with no increase in circulating insulin. Our results suggest that a single drink of KE may acutely improve metabolic control in individuals with obesity. Future research is warranted to examine whether KE could be used safely to have longer-term effects on metabolic control. This trial was registered at clinicaltrials.gov as NCT03461068.

Indexed as

3-Hydroxybutyric AcidAdultBlood GlucoseDietary SupplementsFemaleGlucagonGlucagon-Like Peptide 1Glucose Tolerance TestGlycemic IndexHumansKetonesMaleMiddle AgedObesity3-Hydroxybutyric AcidBlood GlucoseGlucagonGlucagon-Like Peptide 1Ketonescarbohydrate metabolismglycemic controlinsulin resistanceketone supplementobesityβ-hydroxybutyrate

Identifiers

PMID31599919
PMCPMC6885474
OpenAlexW2979390634

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.