Evidence map›Paper›PMID 41714145›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2026

Delayed, Reduced, and Redundant: Information Processing of Prediction Errors during Human Sleep.

Christine Blume, Marina Dauphin, Maria Niedernhuber, Manuel Spitschan, Martin P Meyer, Christian Cajochen, Tristan Bekinschtein, Andrés Canales-Johnson

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Broadband synergy versus oscillatory redundancy in the visual cortex.bioRxiv : the preprint server for biology · 2025
    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

8 authors.

Christine BlumeCentre for Chronobiology, Psychiatric Hospital of the University of Basel, Basel 4002, Switzerland christine.blume@unibas.ch afc37@cam.ac.uk.ORCID 0000-0003-2328-9612
Marina DauphinConsciousness and Cognition Lab, Department of Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom.
Maria NiedernhuberConsciousness and Cognition Lab, Department of Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom.ORCID 0000-0002-4459-6796
Manuel SpitschanTranslational Sensory and Circadian Neuroscience, Max Planck Institute for Biological Cybernetics, Tübingen 72076, Germany.
Martin P MeyerPsychiatric Hospital of the University of Basel, Basel 4002, Switzerland.
Christian CajochenCentre for Chronobiology, Psychiatric Hospital of the University of Basel, Basel 4002, Switzerland.
Tristan BekinschteinConsciousness and Cognition Lab, Department of Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom.
Andrés Canales-JohnsonConsciousness and Cognition Lab, Department of Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom christine.blume@unibas.ch afc37@cam.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During sleep, the human brain transitions to a "sentinel processing mode," enabling the continued processing of environmental stimuli despite the absence of consciousness. We employed advanced information-theoretic analyses, including mutual information (MI) and co-information (co-I), alongside event-related potential (ERP) and temporal generalization analyses (TGA), to characterize auditory prediction error processing across wakefulness and sleep. We hypothesized that a shared neural code would be present across sleep stages, with deeper sleep being associated with reduced information content and increased information redundancy. Twenty-nine participants (15 women) underwent an auditory "local-global" oddball paradigm during wakefulness and an 8 h sleep opportunity monitored via polysomnography. We focused on "local" mismatch responses to a deviating fifth tone after four standards. ERP analyses showed that prediction error processing continued throughout all sleep stages (N1-N3, REM). Mutual information analyses revealed a substantial reduction in encoded prediction error information particularly during N3 and REM, although ERP amplitudes increased with deeper NREM sleep. We also observed delayed information encoding during sleep, and co-information analyses showed neural dynamics became increasingly redundant with increasing sleep depth. TGA revealed a largely shared neural code between N2 and N3, though it differed between wakefulness and sleep. We demonstrate how the neural code of the "sentinel processing mode" changes from wake to light to deep sleep and REM, characterized by delayed processing, more redundant and less rich neural information in the human cortex as consciousness wanes. This altered stimulus processing reveals how neural information evolves with variations in consciousness across the night.

Indexed as

Auditory PerceptionBrainSleepSleep StagesAcoustic StimulationAdultElectroencephalographyEvoked PotentialsEvoked Potentials, AuditoryFemaleHumansMalePolysomnographyWakefulnessYoung Adultconsciousnessinformation decompositionoddballprediction errorsensory processingsleep

Identifiers

PMID41714145
PMCPMC13000989

What OpenQuestion holds

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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.