Evidence map›Paper›PMID 40675150›Full record

ArticleCurrent biology : CB2025

Cortical activity upon awakening from sleep reveals consistent spatio-temporal gradients across sleep stages in human EEG.

Aurélie M Stephan, Jacinthe Cataldi, Amrita Singh Virk, Francesca Siclari

Abstract read
In one paragraph

Article in Current biology : CB, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Association between sleep inertia and cognitive performance among older adults in the Wisconsin Sleep Cohort study.Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2026
    Article
  3. Article
  4. 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

4 authors.

Aurélie M StephanCenter for Investigation and Research on Sleep, Lausanne University Hospital, 1011 Lausanne, Switzerland; The Sense Innovation and Research Center, 1007 Lausanne and Sion, Switzerland; The Netherlands Institute for Neuroscience, 1105 BA Amsterdam, the Netherlands.
Jacinthe CataldiCenter for Investigation and Research on Sleep, Lausanne University Hospital, 1011 Lausanne, Switzerland; The Sense Innovation and Research Center, 1007 Lausanne and Sion, Switzerland.
Amrita Singh VirkCenter for Investigation and Research on Sleep, Lausanne University Hospital, 1011 Lausanne, Switzerland.
Francesca SiclariCenter for Investigation and Research on Sleep, Lausanne University Hospital, 1011 Lausanne, Switzerland; The Sense Innovation and Research Center, 1007 Lausanne and Sion, Switzerland; The Netherlands Institute for Neuroscience, 1105 BA Amsterdam, the Netherlands. Electronic address: f.siclari@nin.knaw.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

How does the brain awaken from sleep? Several studies have suggested that the awakening process occurs asynchronously across brain regions, but the precise nature of these changes and how they are reflected in human electroencephalography (EEG) remains unknown. Here, we recorded 1,073 awakenings and arousals with high-density EEG and mapped brain activity at a second-to-second timescale around movement onset using source modeling. We found that cortical activity upon awakening progressed along highly consistent spatial and frequency gradients. In awakenings and arousals from non-rapid eye movement (NREM) sleep, transient increases in low-frequency power preceded increases in high-frequency power by a few seconds, whereas awakenings from REM sleep were mainly characterized by increases in high-frequency power. Regardless of sleep stage, high-frequency changes were first seen in frontal and last in occipital and inferior-temporal cortical areas, whereas low-frequency changes in NREM sleep started in a centro-parietal "hotspot," progressed frontally, and reached occipital and inferior-temporal regions last. Finally, the presence of these spatio-temporal arousal patterns during sleep, before participants were awakened by sounds, was followed by lower sleepiness ratings upon awakening. These results indicate a consistent spatio-temporal EEG signature of the awakening process that likely reflects the structural organization of arousal systems. Importantly, a transient increase in slow EEG frequencies, which are normally associated with sleep, is inherent to the arousal process and functionally correlates with feeling more awake when awakening from NREM sleep. These findings have important implications for the interpretation of arousal signals and the detection of incomplete awakenings in sleep disorders.

Indexed as

ArousalCerebral CortexSleep StagesWakefulnessAdultElectroencephalographyFemaleHumansMaleSleepYoung Adultarousalawakeningconsciousnesshigh-density EEGsleepsleep inertiasleepinesssleep slow wavessleep-to-wake transitionwake-like activity

Identifiers

PMID40675150
PMCPMC12459234

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Registered trials

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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.