Evidence map›Paper›PMID 41872325›Full record

ArticleCommunications medicine2026

Deep learning using electroencephalogram (EEG) data for diagnosing and predicting SSRI response in major depressive disorder.

Sebastian Olbrich, Natalia Jaworska, Sara de la Salle, Verner Knott, Pierre Blier, Martin Brunovsky, Tobias Welt, Mateo de Bardeci, Cheng Teng-Ip

Abstract read
In one paragraph

Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

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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

9 authors.

Sebastian OlbrichUniversity of Zurich, Psychiatric Hospital, Zurich, Switzerland. sebastian.olbrich@pukzh.ch.ORCID http://orcid.org/0000-0001-5557-4878
Natalia JaworskaUniversity of Ottawa Institute of Mental Health Research at The Royal, Ottawa, ON, Canada.
Sara de la SalleUniversity of Ottawa Institute of Mental Health Research at The Royal, Ottawa, ON, Canada.
Verner KnottUniversity of Ottawa Institute of Mental Health Research at The Royal, Ottawa, ON, Canada.
Pierre BlierUniversity of Ottawa Institute of Mental Health Research at The Royal, Ottawa, ON, Canada.
Martin BrunovskyNational Institute of Mental Health, Klecany & Third Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID http://orcid.org/0000-0002-2483-0848
Tobias WeltUniversity of Zurich, Psychiatric Hospital, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-4793-9061
Mateo de BardeciUniversity of Zurich, Psychiatric Hospital, Zurich, Switzerland.
Cheng Teng-IpCenter for Cognitive and Brain Sciences, University of Macau, Taipa, Macau, SAR, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajor Depression (MDD) is a potentially life-threatening condition that ranks among the diseases with the highest global burden. Despite its prevalence, current diagnostic methods remain largely subjective, and first-line treatments exhibit high rates of non-responders.

methodsThis study investigates the application of deep learning (DL) algorithms to electroencephalogram (EEG) data for the MDD-diagnosis and prediction of treatment outcomes following the administration of selective serotonin reuptake inhibitors (SSRIs), using six large, independent datasets with a total of n = 146 for healthy subjects and n = 203 for patients. DL models were trained on one portion of the datasets and tested on unseen data from different subjects. To interpret the classification features, Gradient-weighted Class Activation Mapping (Grad-CAM) was applied.

resultsThe models achieve an average accuracy of 67.5% (best fold 70%) in distinguishing MDD patients from healthy controls and mean 79% accuracy (best fold 85%) in predicting SSRI responders. Key EEG markers for both classification tasks revealed by Grad-CAM include alpha activity in the frontal and parietal regions. Simulation of a clinical decision scenario for SSRI treatment selection indicates a number needed to treat (NNT) of five when using a model with 80% predictive accuracy, corresponding to an increase in treatment response from a 50% baseline to 70% with model-guided selection.

conclusionThese findings underscore the clinical potential of EEG-based DL models for stratified treatment in MDD, facilitating accurate therapy choices and reducing ineffective treatments. The results of the integration of objective neurophysiological markers into clinical psychiatry are indicating the potential for more personalized treatment allocation.

Identifiers

PMID41872325
PMCPMC13009148

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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.