Evidence map›Paper›PMID 33410985›Full record

ArticlePsychopharmacology2021

Effects of ketogenic diet and ketone monoester supplement on acute alcohol withdrawal symptoms in male mice.

Annika Billefeld Bornebusch, Graeme F Mason, Simone Tonetto, Jakob Damsgaard, Albert Gjedde, Anders Fink-Jensen, Morgane Thomsen

2 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in Psychopharmacology, 2021. 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.0field-weighted citation impact, top 8% 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.

NCT03255031 nacompletednot on this map

Ketogenic Diet (KD) in Alcoholism

TypeinterventionalSponsorNational Institute on Alcohol Abuse and Alcoholism (NIAAA)Ran2017 to 2023Enrolled53ConditionsAlcoholismArmsKetogenic Diet (KD), Standard American (SA) Meals and Shakes
NCT03878225 naunknown statusnot on this map

The Ketone Mono Ester Study - Does a Ketogenic Dietary Supplement Reduce Alcohol Withdrawal Symptoms in Humans

TypeinterventionalSponsorAnders Fink-Jensen, MD, DMSciRan2020 to 2022Enrolled36ConditionsAlcohol Use Disorder, Alcohol Withdrawal, KetosisArmsH.V.M.N. Ketone Ester, Placebo
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 29 citations in OpenAlex.

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  3. Reversible alterations of brain acetate metabolism associated with alcohol consumption.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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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

7 authors at 4 institutions in 2 countries.

Annika Billefeld BornebuschLaboratory of Neuropsychiatry, Psychiatric Center Copenhagen, Rigshospitalet, Mental Health Services-Capital Region of Denmark, Edel Sauntes Allé 10, DK-2100, Copenhagen, Denmark.
Graeme F MasonDepartments of Radiology & Biomedical Imaging, Psychiatry, and Biomedical Engineering, Yale University, New Haven, CT, USA.
Simone TonettoLaboratory of Neuropsychiatry, Psychiatric Center Copenhagen, Rigshospitalet, Mental Health Services-Capital Region of Denmark, Edel Sauntes Allé 10, DK-2100, Copenhagen, Denmark.
Jakob DamsgaardLaboratory of Neuropsychiatry, Psychiatric Center Copenhagen, Rigshospitalet, Mental Health Services-Capital Region of Denmark, Edel Sauntes Allé 10, DK-2100, Copenhagen, Denmark.
Albert GjeddeDepartment of Nuclear Medicine, Odense University Hospital, University of Southern Denmark, Odense, Denmark.
Anders Fink-JensenLaboratory of Neuropsychiatry, Psychiatric Center Copenhagen, Rigshospitalet, Mental Health Services-Capital Region of Denmark, Edel Sauntes Allé 10, DK-2100, Copenhagen, Denmark.
Morgane ThomsenLaboratory of Neuropsychiatry, Psychiatric Center Copenhagen, Rigshospitalet, Mental Health Services-Capital Region of Denmark, Edel Sauntes Allé 10, DK-2100, Copenhagen, Denmark. morgane.hermann.thomsen@regionh.dk.ORCID http://orcid.org/0000-0002-7250-6006
Mental Health Services · DKUniversity of Copenhagen · DKUniversity of Southern Denmark · DKYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Brain Acetate and Ethanol Metabolism in Alcohol Dependence and AbuseR01AA021984 · NIAAA · YALE UNIVERSITY · PI MASON, GRAEME F. · 2013 to 2017
$2.7M
Comprehensive, Cross Platform-Validated 13C Flux Measures of Intra-and Inter-tissue MetabolismR01DK108283 · NIDDK · YALE UNIVERSITY · PI KIBBEY, RICHARD G, MASON, GRAEME F. · 2016 to 2019
$2.1M
Glucagon-like peptide-1 modulation of alcohol effectsR01AA025071 · NIAAA · REGION HOVEDSTADEN · PI THOMSEN, MORGANE HERMANN · 2017 to 2022
$627k
Ivan Nielsen Foundation (DK) n/aNCATS NIH HHS UL1 TR001863NIAAA NIH HHS R01 AA021984NIAAA NIH HHS R01AA021984NIAAA NIH HHS R01 AA025071NIAAA NIH HHS R01AA025071NIDDK NIH HHS R01 DK108283NIDDK NIH HHS R01DK108283Region Hovedstaden n/aSundhed og Sygdom, Det Frie Forskningsråd 0134-00044B
6 · The paper itself

Abstract

rationaleAfter alcohol ingestion, the brain partly switches from consumption of glucose to consumption of the alcohol metabolite acetate. In heavy drinkers, the switch persists after abrupt abstinence, leading to the hypothesis that the resting brain may be "starved" when acetate levels suddenly drop during abstinence, despite normal blood glucose, contributing to withdrawal symptoms. We hypothesized that ketone bodies, like acetate, could act as alternative fuels in the brain and alleviate withdrawal symptoms.

objectivesWe previously reported that a ketogenic diet during alcohol exposure reduced acute withdrawal symptoms in rats. Here, our goals were to test whether (1) we could reproduce our findings, in mice and with longer alcohol exposure; (2) ketone bodies alone are sufficient to reduce withdrawal symptoms (clarifying mechanism); (3) introduction of ketogenic diets at abstinence (a clinically more practical implementation) would also be effective.

methodsMale C57BL/6NTac mice had intermittent alcohol exposure for 3 weeks using liquid diet. Somatic alcohol withdrawal symptoms were measured as handling-induced convulsions; anxiety-like behavior was measured using the light-dark transition test. We tested a ketogenic diet, and a ketone monoester supplement with a regular carbohydrate-containing diet.

resultsThe regular diet with ketone monoester was sufficient to reduce handling-induced convulsions and anxiety-like behaviors in early withdrawal. Only the ketone monoester reduced handling-induced convulsions when given during abstinence, consistent with faster elevation of blood ketones, relative to ketogenic diet.

conclusionsThese findings support the potential utility of therapeutic ketosis as an adjunctive treatment in early detoxification in alcohol-dependent patients seeking to become abstinent.

trial registrationclinicaltrials.gov NCT03878225, NCT03255031.

Indexed as

Diet, KetogenicAlcoholismAnimalsAnxietyBrainClinical Trials as TopicDietary SupplementsEthanolGlucoseHumansKetone BodiesKetonesMaleMiceMice, Inbred C57BLRatsEthanolGlucoseKetone BodiesKetonesAlcohol dependenceAlcoholismAlcohol withdrawalAnxiety-like behaviorDetoxificationEthanolKetone bodiesKetone monoesterMice

Identifiers

PMID33410985
PMCPMC7914216
OpenAlexW3119601769

What OpenQuestion holds

Textmetadata
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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.