Evidence map›Paper›PMID 39725743›Full record

ArticleMolecular psychiatry2025

Clinical response to neurofeedback in major depression relates to subtypes of whole-brain activation patterns during training.

Masaya Misaki, Kymberly D Young, Aki Tsuchiyagaito, Jonathan Savitz, Salvador M Guinjoan

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Masaya MisakiLaureate Institute for Brain Research, Tulsa, OK, USA. mmisaki@laureateinstitute.org.ORCID 0000-0002-6829-4311
Kymberly D YoungDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0001-5133-2142
Aki TsuchiyagaitoLaureate Institute for Brain Research, Tulsa, OK, USA.ORCID 0000-0002-7606-1745
Jonathan SavitzLaureate Institute for Brain Research, Tulsa, OK, USA.ORCID 0000-0001-8143-182X
Salvador M GuinjoanLaureate Institute for Brain Research, Tulsa, OK, USA.ORCID 0000-0002-1958-4259

Funding

The Center for Neuroscience-based Mental Health Assessment and Prediction (NEUROMAP)P20GM121312 · NIGMS · LAUREATE INSTITUTE FOR BRAIN RESEARCH · PI Masaya Misaki · 2017 to 2026
$23.7M
Acute modulation of neural circuitry regulating immune function in depressionR21MH113871 · NIMH · LAUREATE INSTITUTE FOR BRAIN RESEARCH · PI SAVITZ, JONATHAN · 2018 to 2019
$477k
Effects of amygdala neurofeedback on depressive symptoms and processing biasesK99MH101235 · NIMH · LAUREATE INSTITUTE FOR BRAIN RESEARCH · PI YOUNG, KYM · 2014 to 2015
$179k
Brain and Behavior Research Foundation (Brain & Behavior Research Foundation) NARSAD Young Investigator GrantNIGMS NIH HHS P20 GM121312NIMH NIH HHS K99 MH101235NIMH NIH HHS R21 MH113871
6 · The paper itself

Abstract

Major Depressive Disorder (MDD) poses a significant public health challenge due to its high prevalence and the substantial burden it places on individuals and healthcare systems. Real-time functional magnetic resonance imaging neurofeedback (rtfMRI-NF) shows promise as a treatment for this disorder, although its mechanisms of action remain unclear. This study investigated whole-brain response patterns during rtfMRI-NF training to explain interindividual variability in clinical efficacy in MDD. We analyzed data from 95 participants (67 active, 28 control) with MDD from previous rtfMRI-NF studies designed to increase left amygdala activation through positive autobiographical memory recall. Significant symptom reduction was observed in the active group (t = -4.404, d = -0.704, p < 0.001) but not in the control group (t = -1.609, d = -0.430, p = 0.111). However, left amygdala activation did not account for the variability in clinical efficacy. To elucidate the brain training process underlying the clinical effect, we examined whole-brain activation patterns during two critical phases of the neurofeedback procedure: activation during the self-regulation period, and transient responses to feedback signal presentations. Using a systematic process involving feature selection, manifold extraction, and clustering with cross-validation, we identified two subtypes of regulation activation and three subtypes of brain responses to feedback signals. These subtypes were significantly associated with the clinical effect (regulation subtype: F = 8.735, p = 0.005; feedback response subtype: F = 5.326, p = 0.008; subtypes' interaction: F = 3.471, p = 0.039). Subtypes associated with significant symptom reduction were characterized by selective increases in control regions, including lateral prefrontal areas, and decreases in regions associated with self-referential thinking, such as default mode areas. These findings suggest that large-scale brain activity during training is more critical for clinical efficacy than the level of activation in the neurofeedback target region itself. Tailoring neurofeedback training to incorporate these patterns could significantly enhance its therapeutic efficacy.

Indexed as

Major Depressive DisorderNeurofeedbackAdultAmygdalaBrainBrain MappingFemaleHumansMagnetic Resonance ImagingMaleMemory, EpisodicMiddle AgedTreatment OutcomeYoung Adult

Identifiers

PMID39725743
PMCPMC12092192

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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.