Evidence map›Paper›PMID 34904800›Full record

Trial reportTrends in psychiatry and psychotherapy2023

Brain-derived neurotrophic factor serum levels following ketamine and esketamine intervention for treatment-resistant depression: secondary analysis from a randomized trial.

Ana Teresa Caliman-Fontes, Gustavo C Leal, Fernanda S Correia-Melo, Camilla S Paixão, Michelle S Carvalho, Ana Paula Jesus-Nunes, Flavia Vieira, Guilherme Magnavita, Igor D Bandeira, Rodrigo P Mello and 10 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Trends in psychiatry and psychotherapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 pooled it
–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

12 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Review
  7. Psychedelics in treatment-resistant depression: a comprehensive review of mechanisms, clinical evidence, and recommendations.Neuropsychiatrie : Klinik, Diagnostik, Therapie und Rehabilitation : Organ der Gesellschaft Osterreichischer Nervenarzte und Psychiater · 2026
    Review
  8. Review
  9. Review
  10. Review
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  12. Article
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

20 authors.

Ana Teresa Caliman-FontesFaculdade de Medicina da Bahia, Universidade Federal da Bahia (UFBA), Salvador, BA, Brazil. Laboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Gustavo C LealLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Serviço de Psiquiatria, Hospital Universitário Professor Edgard Santos, UFBA, Salvador, BA, Brazil. Programa de Pós-Graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Fernanda S Correia-MeloLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Programa de Pós-Graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Camilla S PaixãoLaboratório de Pesquisas Clínicas, Instituto Gonçalo Moniz, Fiocruz, Salvador, BA, Brazil. Serviço de Imunologia, UFBA, Salvador, BA, Brazil.
Michelle S CarvalhoLaboratório Interdisciplinar de Neurociências Clínicas, Universidade Federal de São Paulo, São Paulo, Brazil.
Ana Paula Jesus-NunesLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Programa de Pós-Graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Flavia VieiraLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Programa de Pós-Graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Guilherme MagnavitaLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Igor D BandeiraLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Programa de Pós-Graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Rodrigo P MelloLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Programa de Pós-Graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Graziele BeanesLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Programa de Pós-Graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Samantha S SilvaLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Serviço de Psiquiatria, Hospital Universitário Professor Edgard Santos, UFBA, Salvador, BA, Brazil.
Mariana EchegarayLaboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Lucas P CarvalhoLaboratório de Pesquisas Clínicas, Instituto Gonçalo Moniz, Fiocruz, Salvador, BA, Brazil. Serviço de Imunologia, UFBA, Salvador, BA, Brazil.
Paulo MachadoLaboratório de Pesquisas Clínicas, Instituto Gonçalo Moniz, Fiocruz, Salvador, BA, Brazil. Serviço de Imunologia, UFBA, Salvador, BA, Brazil.
Aline S SampaioFaculdade de Medicina da Bahia, Universidade Federal da Bahia (UFBA), Salvador, BA, Brazil. Laboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.
Taiane de A CardosoDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.
Flávio KapczinskiMood Disorders Program, Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.
Acioly L T LacerdaLaboratório Interdisciplinar de Neurociências Clínicas, Universidade Federal de São Paulo, São Paulo, Brazil.
Lucas C QuarantiniFaculdade de Medicina da Bahia, Universidade Federal da Bahia (UFBA), Salvador, BA, Brazil. Laboratório de Neuropsicofarmacologia, Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil. Serviço de Psiquiatria, Hospital Universitário Professor Edgard Santos, UFBA, Salvador, BA, Brazil. Programa de Pós-Graduação em Medicina e Saúde, Faculdade de Medicina da Bahia, UFBA, Salvador, BA, Brazil.

Funding

CAPES 001PPSUS 003/2017
6 · The paper itself

Abstract

objectivesEvidence suggests that ketamine's influence on brain-derived neurotrophic factor (BDNF) might be involved in its mechanism of rapid antidepressant action. We aimed to evaluate the differential impact of ketamine and esketamine on serum BDNF levels and its association with response patterns in treatment-resistant depression (TRD).

methodsParticipants (n = 53) are from a randomized, double-blind clinical trial comparing the efficacy of single-dose ketamine (0.5mg/kg, n = 27) and esketamine (0.25mg/kg, n = 26) in TRD. Depression severity was assessed before and 24 hours, 72 hours, and 7 days after the intervention, using the Montgomery-Åsberg Depression Rating Scale (MADRS). Blood samples were collected before infusion, 24 hours, and 7 days afterwards.

resultsThere were no significant changes in BDNF levels at post-infusion evaluation points, and no difference in BDNF levels comparing ketamine and esketamine. Both drugs exhibited similar therapeutic effect. There was no association between BDNF levels and response to treatment or severity of depressive symptoms.

conclusionThere was no significant treatment impact on BDNF serum levels - neither with ketamine nor esketamine - despite therapeutic response. These results suggest that ketamine or esketamine intervention for TRD has no impact on BDNF levels measured at 24 hours and 7 days after the infusion.

Indexed as

Depressive Disorder, Treatment-ResistantKetamineBrain-Derived Neurotrophic FactorDepressionHumansBrain-Derived Neurotrophic FactorEsketamineKetamineBDNFbiochemical markersmajor depressive disorderneurotrophinsNMDA antagonists

Identifiers

PMID34904800
PMCPMC9991420

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Registered trials

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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.