Evidence mapPaperPMID 41248397Full record

ArticleBMJ open2025

Feasibility and acceptability of 8-week oral tributyrin supplementation as add on to antidepressant medication in patients with depression: a study protocol paper for a pilot, randomised controlled trial.

Vera Korenblik, Aniko Korosi, Stanley Brul, Claudi Bockting, Max Nieuwdorp, Anja Lok

Abstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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

6 authors.

Vera KorenblikDepartment of Psychiatry, Amsterdam University Medical Centre, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0001-5254-6345
Aniko KorosiCentre for Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0001-9701-3331
Stanley BrulCentre for Urban Mental Health, University of Amsterdam, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0001-5706-8768
Claudi BocktingDepartment of Psychiatry, Amsterdam University Medical Centre, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-9220-9244
Max NieuwdorpDepartment of Internal and Vascular Medicine, Amsterdam University Medical Centre, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-1926-7659
Anja LokDepartment of Psychiatry, Amsterdam University Medical Centre, Amsterdam, the Netherlands a.lok@amsterdamumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajor depressive disorder (MDD) is a severe mental health condition that profoundly affects both psychological and physical well-being. Growing evidence indicates that targeting the gut-brain axis could present new therapeutic opportunities for MDD, given the role of gut microbiota and their metabolites in its pathophysiology. One promising approach involves supplementation with butyrate, a short-chain fatty acid that has demonstrated antidepressant potential in preclinical models of depression. However, clinical research exploring the effects of butyrate supplementation in individuals with MDD remains lacking.

methodsThis study is a double-blind, parallel, 1:1 randomised placebo-controlled trial. The primary aim of this pilot study is to assess the feasibility and acceptability of an 8-week oral supplementation with tributyrin, a triglyceride form of butyrate (4 g/day), added to usual treatment with antidepressant medication in 24 patients with mild-to-severe MDD aged 18-65 years. Secondary outcomes include changes in depressive symptoms, assessed weekly throughout the supplementation period and at 16 weeks post-supplementation during follow-up, as well as changes in anhedonia and affect, measured multiple times per day via a smartphone application throughout the supplementation period. Additional outcomes include changes in gastrointestinal symptoms, changes in faecal microbiome, metabolites in blood and faeces, inflammation, epigenetic markers, stress and intestinal permeability. ETHICS AND DISSEMINATION: The study has been approved by the Medical Research Ethics Committee of the Amsterdam University Medical Centre, the Netherlands. DISCUSSION: Should the pilot demonstrate feasibility and acceptability, a larger-scale study will be warranted to evaluate the efficacy of tributyrin supplementation in alleviating depressive symptoms. This pilot will provide valuable insights to guide sample size calculations and refine study design for subsequent trials. Ultimately, this research could lead to novel adjunctive treatments for MDD targeting gut-brain signalling, offering new therapeutic avenues for patients with MDD. TRIAL REGISTRATION NUMBER: This trial has been registered in the International Clinical Trials Registry Platform (registry number: NL-OMON57116).

Indexed as

Antidepressive AgentsDietary SupplementsMajor Depressive DisorderTriglyceridesAdministration, OralAdolescentAdultAgedDouble-Blind MethodDrug Therapy, CombinationFeasibility StudiesFemaleGastrointestinal MicrobiomeHumansMaleMiddle AgedAntidepressive AgentstributyrinTriglyceridesDepression & mood disordersMicrobiotaNUTRITION & DIETETICSPSYCHIATRY

Identifiers

PMID41248397
PMCPMC12587968

What Socratic holds

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Registered trials

None linked

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 Socratic graph.