Evidence map›Paper›PMID 38816586›Full record

ReviewMolecular psychiatry2024

Beyond the serotonin deficit hypothesis: communicating a neuroplasticity framework of major depressive disorder.

Chloe E Page, C Neill Epperson, Andrew M Novick, Korrina A Duffy, Scott M Thompson

Abstract readReview
In one paragraph

Review in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 2 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

38 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  15. A Time-Sensitive Plasticity Distinguishes the Rapid and Sustained Synaptic Actions of Ketamine from Its (2The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
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  20. Ascorbic acid enhances antidepressant-like efficacy of esketamine: Hippocampal TARP-γ8-containing AMPA receptors mediate synaptic modulation.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    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

5 authors.

Chloe E PageDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID 0000-0001-5573-3760
C Neill EppersonDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Andrew M NovickDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Korrina A DuffyDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID 0000-0003-0377-0134
Scott M ThompsonDepartment of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, USA. scott.m.thompson@cuanschutz.edu.ORCID 0000-0001-9844-9049

Funding

Neurobiology of hormonal contraceptionK23HD110435 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Andrew Michael Novick · 2023 to 2026
$643k
NICHD NIH HHS K23 HD110435NICHD NIH HHS L30 HD106379
6 · The paper itself

Abstract

The serotonin deficit hypothesis explanation for major depressive disorder (MDD) has persisted among clinicians and the general public alike despite insufficient supporting evidence. To combat rising mental health crises and eroding public trust in science and medicine, researchers and clinicians must be able to communicate to patients and the public an updated framework of MDD: one that is (1) accessible to a general audience, (2) accurately integrates current evidence about the efficacy of conventional serotonergic antidepressants with broader and deeper understandings of pathophysiology and treatment, and (3) capable of accommodating new evidence. In this article, we summarize a framework for the pathophysiology and treatment of MDD that is informed by clinical and preclinical research in psychiatry and neuroscience. First, we discuss how MDD can be understood as inflexibility in cognitive and emotional brain circuits that involves a persistent negativity bias. Second, we discuss how effective treatments for MDD enhance mechanisms of neuroplasticity-including via serotonergic interventions-to restore synaptic, network, and behavioral function in ways that facilitate adaptive cognitive and emotional processing. These treatments include typical monoaminergic antidepressants, novel antidepressants like ketamine and psychedelics, and psychotherapy and neuromodulation techniques. At the end of the article, we discuss this framework from the perspective of effective science communication and provide useful language and metaphors for researchers, clinicians, and other professionals discussing MDD with a general or patient audience.

Indexed as

Major Depressive DisorderNeuronal PlasticitySerotoninAntidepressive AgentsBrainHumansAntidepressive AgentsSerotonin

Identifiers

PMID38816586
PMCPMC11692567

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

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.