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Positive with limitationsBaseline resting-state EEG study with 12-week clinical outcome classification and nested cross-validation

Machine learning-based source-level EEG functional network biomarkers of antidepressant treatment response in major depressive disorder.

Baseline EEG network features distinguished later antidepressant responders from nonresponders within this research sample. The model has not yet been validated as a clinical test for selecting medication.

Song YW, Lee HA, Kim S, Kim JS.
Progress in Neuro-Psychopharmacology & Biological Psychiatry · Publication date: 2026-10-02
Added to site: 2026-10-03
DOI: 10.1016/j.pnpbp.2026.111957

Publication date verified in PubMed. This source date is separate from the site's addition date.

Modalities
EEG, Source-level EEG, Machine learning
Clinical focus
Major depressive disorder, Treatment-response biomarkers, Functional connectivity
Population
Patients with major depressive disorder and a healthy comparison group; age and treatment-regimen details were not exposed in the checked abstract
Sample
47 patients with major depressive disorder and 41 healthy controls; 20 patients were classified as responders and 27 as nonresponders
Intervention / method
Baseline source-level EEG networks were characterized with graph measures, then nodal features were used in nested cross-validation to classify response after 12 weeks
Comparator
Antidepressant responders, defined by at least 50% Hamilton Depression Rating Scale reduction, versus nonresponders; healthy controls informed selected comparisons

Clinician summary

A support-vector machine using nodal network features reached 82.98% accuracy, 85.19% sensitivity and 80.00% specificity in nested cross-validation. High-beta network measures differed between responders and nonresponders, and responder theta-band clustering differed from healthy controls.

How to interpret the findings

Only 47 patients contributed outcome labels, and the model was not tested in an independent external cohort. The abstract does not expose medication standardization, preprocessing choices, feature-selection stability or calibration. Internal cross-validation performance does not establish prospective treatment-selection utility.

Equipment and disclosures

Resting-state EEG and source-level network analysis were used. The checked abstract does not identify the amplifier, channel count, montage, software or commercial system.

The authors declared no known competing interests. Crossref identifies support from the National Research Foundation of Korea and Korea Ministry of Health and Welfare.

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Abstract checked · Checked 2026-10-03

Summary prepared with AI assistance. Source verification does not imply an independent replication or a clinician's endorsement. Read our review method.