SynthesisFrontiers in neuroscience2025
Beyond the label "major depressive disorder"-detailed characterization of study population matters for EEG-biomarker research.
Synthesis in Frontiers in neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Brain oscillation-synchronized stimulation for major depression: a randomized controlled trial comparing EEG-triggered repetitive TMS with standard iTBS (Acronym: BOSSFRONT2).European archives of psychiatry and clinical neuroscience · 2026Trial
- Human biomarker navigator.iMeta · 2026Review
- From EEG signals to quantitative assessment: predicting depression severity using a novel deep learning framework.Scientific reports · 2026Article
- Subject-Wise Depression Screening from Eight-Channel Resting-State EEG Using Asymmetry-Aware Spectral Features and Connectivity Ablation.Sensors (Basel, Switzerland) · 2026Article
- Alpha-band fronto-limbic hyperconnectivity in adolescents with major depression and suicidal ideation.BMC psychiatry · 2026Article
Corrections and comments
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Authors and funding
2 authors.
Funding
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Abstract
Introduction: Major Depressive Disorder (MDD) is a prevalent, multi-faceted psychiatric disorder influenced by a plethora of physiological and environmental factors. Neuroimaging biomarkers such as diagnosis support systems based on electroencephalography (EEG) recordings have the potential to substantially improve its diagnostic procedure. Research on these biomarkers, however, provides inconsistent findings regarding the robustness of specific markers. One potential source of these contradictions that is frequently neglected may arise from the variability in study populations. Methods: This study systematically reviews 66 original studies from the last 5 years that investigate resting-state EEG-biomarker for MDD detection or diagnosis. The study populations are compared regarding demographic factors, diagnostic procedures and medication, as well as neuropsychological characteristics. Furthermore, we investigate the impact these factors have on the biomarkers, if they were included in the analysis. Finally, we provide further insights into the impact of diagnostic choices and the heterogeneity of a study population based on exploratory analyses in two publicly available data sets. Results: We find indeed a large variability in the study populations with respect to all factors included in the review. Furthermore, these factors are often neglected in analyses even though the studies that include them tend to find effects. Discussion: In light of the variability in diagnostic procedures and heterogeneity in neuropsychological characteristics of the study populations, we advocate for more differentiated target variables in biomarker research then simply MDD and healthy control. Furthermore, the study populations need to be more extensively described and analyses need to include this information in order to provide comparable findings.
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