Evidence map›Paper›PMID 38562835›Full record

ArticlebioRxiv : the preprint server for biology2024

Identifying EEG Biomarkers of Depression with Novel Explainable Deep Learning Architectures.

Charles A Ellis, Martina Lapera Sancho, Robyn L Miller, Vince D Calhoun

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Charles A EllisCenter for Translational Research in Neuroimaging and Data Science at Georgia State University, the Georgia Institute of Technology and Emory University, Atlanta GA 30303, USA.ORCID 0000-0002-1547-9996
Martina Lapera SanchoCenter for Translational Research in Neuroimaging and Data Science at Georgia State University, the Georgia Institute of Technology and Emory University, Atlanta GA 30303, USA.ORCID 0009-0005-2779-4001
Robyn L MillerCenter for Translational Research in Neuroimaging and Data Science at Georgia State University, the Georgia Institute of Technology and Emory University, Atlanta GA 30303, USA.ORCID 0000-0002-4679-7567
Vince D CalhounCenter for Translational Research in Neuroimaging and Data Science at Georgia State University, the Georgia Institute of Technology and Emory University, Atlanta GA 30303, USA.ORCID 0000-0001-9058-0747

Funding

Male/Female differences in psychosis and mood disorders:Dynamic imaging-genomic models for characterizing and predicting psychosis and mood dR01MH118695 · NIMH · GEORGIA STATE UNIVERSITY · PI ADALI, TULAY, CALHOUN, VINCE D · 2019 to 2023
$3.8M
Data-driven solutions for temporal, spatial, and spatiotemporal dynamic functional connectivityR01MH123610 · NIMH · GEORGIA STATE UNIVERSITY · PI ADALI, TULAY, CALHOUN, VINCE D · 2021 to 2025
$3.1M
NIMH NIH HHS R01 MH118695NIMH NIH HHS R01 MH123610
6 · The paper itself

Abstract

Deep learning methods are increasingly being applied to raw electroencephalogram (EEG) data. However, if these models are to be used in clinical or research contexts, methods to explain them must be developed, and if these models are to be used in research contexts, methods for combining explanations across large numbers of models must be developed to counteract the inherent randomness of existing training approaches. Model visualization-based explainability methods for EEG involve structuring a model architecture such that its extracted features can be characterized and have the potential to offer highly useful insights into the patterns that they uncover. Nevertheless, model visualization-based explainability methods have been underexplored within the context of multichannel EEG, and methods to combine their explanations across folds have not yet been developed. In this study, we present two novel convolutional neural network-based architectures and apply them for automated major depressive disorder diagnosis. Our models obtain slightly lower classification performance than a baseline architecture. However, across 50 training folds, they find that individuals with MDD exhibit higher β power, potentially higher δ power, and higher brain-wide correlation that is most strongly represented within the right hemisphere. This study provides multiple key insights into MDD and represents a significant step forward for the domain of explainable deep learning applied to raw EEG. We hope that it will inspire future efforts that will eventually enable the development of explainable EEG deep learning models that can contribute both to clinical care and novel medical research discoveries.

Indexed as

Convolutional Neural NetworksElectroencephalographyExplainable AIMajor Depressive Disorder

Identifiers

PMID38562835
PMCPMC10983917

What OpenQuestion holds

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Registered trials

None linked

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.