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

Overview

Authors: Sebastian Olbrich1, Natalia Jaworska2, Sara de la Salle2, Verner Knott2, Pierre Blier2, Martin Brunovsky3, Tobias Welt1, Mateo de Bardeci1, Cheng Teng-Ip4
  1. University of Zurich, Psychiatric Hospital,Zurich, Switzerland
  2. University of Ottawa Institute of Mental Health Research at The Royal,Ottawa, ON Canada
  3. National Institute of Mental Health, Klecany & Third Faculty of Medicine,Charles University Prague, Czech Republic
  4. Center for Cognitive and Brain Sciences, University of Macau, Taipa,Macau, SAR China
Journal: Communications medicine, volume 6, issue 1, article 159
Dates: received 14 October 2024; accepted 12 January 2026; published online 23 March 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1038/s43856-026-01394-z · PMID 41872325 · PMCID PMC13009148 · OpenAlex W7140088162
Open access: gold, a free copy (OpenAlex)
Categories: EEG (modality), human (organism), depression (population), clinical / translational (subfield)
Methods: Spectral & time-frequency, Connectivity, Machine learning, Statistics, Preprocessing, Physiology & signal measures
Keywords: Predictive markers, Depression
Topic: EEG and Brain-Computer Interfaces (Cognitive Neuroscience, Neuroscience), according to OpenAlex
Citations: cited by 1 paper (Europe PMC); 44 references in the paper

Abstract

Background: Major 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.

Methods: This 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.

Results: The 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.Conclusion: These 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.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

No file of the authors' code could be read here: it is described below, and read at its source.

canbind.ca/datareleasecbn01

License: none: the authors keep all their rights
State: the link is dead, verified on 30 September 2026
Evidence: found in the paper
Software Heritage: not checked
Found in: the acknowledgements
Not found: README, license file, CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 30 September 2026: the link is dead (HTTP 404)
  • 30 September 2026: the link is dead (HTTP 404)

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Data

No dataset and no data link were found in the paper.

Data availability

The data that support the findings of this study are available on request from the corresponding author S.O. The data are not publicly available due to them containing information that could compromise research participant privacy/consent. The source data for Fig. 2 is in Supplementary Data 1 and in Supplementary Data 2, the source data for Fig. 4 is in Supplementary Data 2 and in Supplementary Data 3, the source data for Fig. 5 is in Supplementary Data 4.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

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Version 1, 30 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 9 authors, 2 keywords, 3 funders, 44 references.

Cite

This paper

Olbrich, S., Jaworska, N., de la Salle, S., Knott, V., Blier, P., Brunovsky, M., Welt, T., de Bardeci, M., & Teng-Ip, C. (2026). Deep learning using electroencephalogram (EEG) data for diagnosing and predicting SSRI response in major depressive disorder. Communications medicine, 6(1), 159. https://doi.org/10.1038/s43856-026-01394-z

BibTeX

@article{olbrich2026deep,
author = {Olbrich, Sebastian and Jaworska, Natalia and de la Salle, Sara and Knott, Verner and Blier, Pierre and Brunovsky, Martin and Welt, Tobias and de Bardeci, Mateo and Teng-Ip, Cheng},
title = {{Deep learning using electroencephalogram (EEG) data for diagnosing and predicting SSRI response in major depressive disorder}},
journal = {Communications medicine},
year = {2026},
month = mar,
volume = {6},
number = {1},
pages = {159},
publisher = {Nature Publishing Group},
issn = {2730-664X},
doi = {10.1038/s43856-026-01394-z},
url = {https://doi.org/10.1038/s43856-026-01394-z},
pmid = {41872325},
pmcid = {PMC13009148}
}

RIS

TY - JOUR
AU - Olbrich, Sebastian
AU - Jaworska, Natalia
AU - de la Salle, Sara
AU - Knott, Verner
AU - Blier, Pierre
AU - Brunovsky, Martin
AU - Welt, Tobias
AU - de Bardeci, Mateo
AU - Teng-Ip, Cheng
TI - Deep learning using electroencephalogram (EEG) data for diagnosing and predicting SSRI response in major depressive disorder
T2 - Communications medicine
J2 - Commun Med (Lond)
PY - 2026
DA - 2026/03/23
VL - 6
IS - 1
SP - 159
SN - 2730-664X
PB - Nature Publishing Group
DO - 10.1038/s43856-026-01394-z
UR - https://doi.org/10.1038/s43856-026-01394-z
LA - en
ER -

CSL-JSON

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