EEG-based Signatures of Schizophrenia, Depression, and Aberrant Aging: A Supervised Machine Learning Investigation

Author:

Sarisik Elif123ORCID,Popovic David1234ORCID,Keeser Daniel2456ORCID,Khuntia Adyasha23ORCID,Schiltz Kolja1ORCID,Falkai Peter124ORCID,Pogarell Oliver1ORCID,Koutsouleris Nikolaos12467ORCID

Affiliation:

1. Max Planck Fellow Group Precision Psychiatry, Max Planck Institute of Psychiatry , Munich , Germany

2. Department of Psychiatry and Psychotherapy, LMU University Hospital, LMU Munich , Munich , Germany

3. International Max Planck Research School for Translational Psychiatry (IMPRS-TP) , Munich , Germany

4. German Center for Mental Health (DZPG), Partner Site Munich , Munich , Germany

5. NeuroImaging Core Unit Munich (NICUM), LMU University Hospital, LMU Munich , Munich , Germany

6. Munich Center for Neurosciences, LMU Munich , Munich , Germany

7. Institute of Psychiatry, Psychology and Neuroscience, King’s College , London , UK

Abstract

Abstract Background Electroencephalography (EEG) is a noninvasive, cost-effective, and robust tool, which directly measures in vivo neuronal mass activity with high temporal resolution. Combined with state-of-the-art machine learning (ML) techniques, EEG recordings could potentially yield in silico biomarkers of severe mental disorders. Hypothesis Pathological and physiological aging processes influence the electrophysiological signatures of schizophrenia (SCZ) and major depressive disorder (MDD). Study Design From a single-center cohort (N = 735, 51.6% male) comprising healthy control individuals (HC, N = 245) and inpatients suffering from SCZ (N = 250) or MDD (N = 240), we acquired resting-state 19 channel-EEG recordings. Using repeated nested cross-validation, support vector machine models were trained to (1) classify patients with SCZ or MDD and HC individuals and (2) predict age in HC individuals. The age model was applied to patient groups to calculate Electrophysiological Age Gap Estimation (EphysAGE) as the difference between predicted and chronological age. The links between EphysAGE, diagnosis, and medication were then further explored. Study Results The classification models robustly discriminated SCZ from HC (balanced accuracy, BAC = 72.7%, P < .001), MDD from HC (BAC = 67.0%, P < .001), and SCZ from MDD individuals (BAC = 63.2%, P < .001). Notably, central alpha (8–11 Hz) power decrease was the most consistently predictive feature for SCZ and MDD. Higher EphysAGE was associated with an increased likelihood of being misclassified as SCZ in HC and MDD (ρHC = 0.23, P < .001; ρMDD = 0.17, P = .01). Conclusions ML models can extract electrophysiological signatures of MDD and SCZ for potential clinical use. However, the impact of aging processes on diagnostic separability calls for timely application of such models, possibly in early recognition settings.

Funder

Else-Kröner-Fresenius-Stiftung

EKFS-Translational Psychiatry

National Institutes of Health

German Innovation Fund

German Federal Ministry of Education and Research

German Science Foundation

German Ministry of Science

German Ministry of Health

Publisher

Oxford University Press (OUP)

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