Evidence map›Paper›PMID 32561733›Full record

ArticleNature communications2020

Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep.

Jeffrey Hubbard, Thomas C Gent, Marieke M B Hoekstra, Yann Emmenegger, Valerie Mongrain, Hans-Peter Landolt, Antoine R Adamantidis, Paul Franken

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
7.1field-weighted citation impact, top 2% of its field
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

61 citing papers in PubMed, 104 citations in OpenAlex.

  1. Trial
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  7. Early microglial response to amyloid plaques drives sleep loss in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  8. Article
  9. Dynamic Respiration-Neural Coupling in Substantia Nigra across Sleep and Anesthesia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  10. Brain-wide properties of slow waves across vigilance states.Sleep advances : a journal of the Sleep Research Society · 2026
    Article
  11. Article
  12. Article
  13. Thalamic involvement defines distinct slow-wave subtypes in NREM sleep.bioRxiv : the preprint server for biology · 2025
    Article
  14. Article
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  16. Review
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1 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 2 countries.

Jeffrey HubbardCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland. jeffrey.hubbard@unil.ch.ORCID http://orcid.org/0000-0002-0405-9398
Thomas C GentDepartment of Neurology, Inselspital University Hospital Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0002-0478-5461
Marieke M B HoekstraCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Yann EmmeneggerCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Valerie MongrainDepartment of Neuroscience, Université de Montréal, Montreal, QC, Canada.ORCID http://orcid.org/0000-0002-6242-9166
Hans-Peter LandoltInstitute of Pharmacology and Toxicology, University of Zürich, Zurich, Switzerland.ORCID http://orcid.org/0000-0003-0887-9403
Antoine R AdamantidisDepartment of Neurology, Inselspital University Hospital Bern, Bern, Switzerland.
Paul FrankenCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland. paul.franken@unil.ch.ORCID http://orcid.org/0000-0002-2500-2921
University of Lausanne · CHUniversity of Zurich · CHUniversité de Montréal · CAUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sleep-wake driven changes in non-rapid-eye-movement sleep (NREM) sleep (NREMS) EEG delta (δ-)power are widely used as proxy for a sleep homeostatic process. Here, we noted frequency increases in δ-waves in sleep-deprived mice, prompting us to re-evaluate how slow-wave characteristics relate to prior sleep-wake history. We identified two classes of δ-waves; one responding to sleep deprivation with high initial power and fast, discontinuous decay during recovery sleep (δ2) and another unrelated to time-spent-awake with slow, linear decay (δ1). Reanalysis of previously published datasets demonstrates that δ-band heterogeneity after sleep deprivation is also present in human subjects. Similar to sleep deprivation, silencing of centromedial thalamus neurons boosted subsequent δ2-waves, specifically. δ2-dynamics paralleled that of temperature, muscle tone, heart rate, and neuronal ON-/OFF-state lengths, all reverting to characteristic NREMS levels within the first recovery hour. Thus, prolonged waking seems to necessitate a physiological recalibration before typical NREMS can be reinstated.

Indexed as

AnimalsDelta RhythmDisease Models, AnimalHealthy VolunteersHumansMaleMiceSleep DeprivationSleep, Slow-WaveWakefulnessYoung Adult

Identifiers

PMID32561733
PMCPMC7305232
OpenAlexW3036566225

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.