Evidence map›Paper›PMID 41258409›Full record

ArticleCommunications psychology2025

Temporally resolved analyses of aperiodic features track neural dynamics during sleep.

Mohamed S Ameen, Joshua Jacobs, Manuel Schabus, Kerstin Hoedlmoser, Thomas Donoghue

Abstract read
In one paragraph

Article in Communications psychology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Aperiodic Signatures of Stress Sensitivity and Depression Recurrence in Adolescents.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2026
    Article
  2. Article
  3. Article
  4. Aperiodic Activity Reflects Pathologic Waveform Shapes in Focal Epilepsy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  5. Multiple Intrinsic Timescales Govern Distinct Brain States in Human Sleep.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
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

5 authors.

Mohamed S AmeenLaboratory for Sleep, Cognition, and Consciousness research, Center for Cognitive Neuroscience Salzburg, Department of Psychology, University of Salzburg, Salzburg, Austria. mohamed.ameen@plus.ac.at.ORCID http://orcid.org/0000-0003-4147-490X
Joshua JacobsElectrophysiology, Memory, and Navigation Laboratory, Department of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0003-1807-6882
Manuel SchabusLaboratory for Sleep, Cognition, and Consciousness research, Center for Cognitive Neuroscience Salzburg, Department of Psychology, University of Salzburg, Salzburg, Austria.ORCID http://orcid.org/0000-0001-5899-8772
Kerstin HoedlmoserLaboratory for Sleep, Cognition, and Consciousness research, Center for Cognitive Neuroscience Salzburg, Department of Psychology, University of Salzburg, Salzburg, Austria.
Thomas DonoghueElectrophysiology, Memory, and Navigation Laboratory, Department of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0001-5911-0472

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aperiodic (1/f-like) component of electrophysiological data, whereby power systematically decreases with increasing frequency, as quantified by the aperiodic exponent, has been shown to differentiate sleep stages. Previous studies typically measured this exponent over narrow frequency ranges and averaged across sleep stages. A systematic review following PRISMA 2020 guidelines, which identified 16 eligible studies examining aperiodic neural activity during sleep, revealed heterogeneous frequency ranges and methodological approaches across studies. Building on these insights, the present study expands the analysis to include wider frequency ranges and alternative models, such as detecting 'knees' in the aperiodic component, which reflect bends in the power spectrum indicating changes in the exponent. Additionally, we applied time-resolved analyses to examine the dynamic patterns of aperiodic activity during sleep. We analyzed data from two sources: intracranial EEG (iEEG) from 106 epilepsy patients and high-density EEG from 17 healthy individuals and compared different frequency ranges and model forms of aperiodic activity. Results showed that broadband aperiodic models and the inclusion of a 'knee' feature effectively captured sleep stage-dependent differences in aperiodic activity. The knee parameter exhibited stage-specific variations, indicating different processing timescales across sleep stages. Time-resolved analysis of the aperiodic exponent tracked sleep stage transitions and responses to external stimuli, highlighting rapidly varying temporal dynamics during sleep. These findings offer valuable insights into brain dynamics during sleep and reveal novel insights and interpretations for understanding aperiodic neural activity during sleep.

Identifiers

PMID41258409
PMCPMC12630853

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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.