Evidence map›Paper›PMID 33743012›Full record

ArticleSleep2021

Occipital sleep spindles predict sequence learning in a visuo-motor task.

Nicolas D Lutz, Marie Admard, Elsa Genzoni, Jan Born, Karsten Rauss

Open access · bronzeAbstract read
In one paragraph

Article in Sleep, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Sleep shapes the associative structure underlying pattern completion in multielement event memory.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Article
  5. Sleep consolidates stimulus-response learning.Learning & memory (Cold Spring Harbor, N.Y.) · 2023
    Article
  6. 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 at 3 institutions in 2 countries.

Nicolas D LutzInstitute of Medical Psychology and Behavioral Neurobiology, University of Tübingen, Tübingen, Germany.ORCID 0000-0002-8451-2630
Marie AdmardInstitute of Medical Psychology and Behavioral Neurobiology, University of Tübingen, Tübingen, Germany.
Elsa GenzoniInstitute of Medical Psychology and Behavioral Neurobiology, University of Tübingen, Tübingen, Germany.
Jan BornInstitute of Medical Psychology and Behavioral Neurobiology, University of Tübingen, Tübingen, Germany.
Karsten RaussInstitute of Medical Psychology and Behavioral Neurobiology, University of Tübingen, Tübingen, Germany.ORCID 0000-0003-3968-772X
University of Tübingen · DEDeutsches Diabetes-Zentrum e.V. · DEÉcole Polytechnique Fédérale de Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

STUDY

objectivesThe brain appears to use internal models to successfully interact with its environment via active predictions of future events. Both internal models and the predictions derived from them are based on previous experience. However, it remains unclear how previously encoded information is maintained to support this function, especially in the visual domain. In the present study, we hypothesized that sleep consolidates newly encoded spatio-temporal regularities to improve predictions afterwards.

methodsWe tested this hypothesis using a novel sequence-learning paradigm that aimed to dissociate perceptual from motor learning. We recorded behavioral performance and high-density electroencephalography (EEG) in male human participants during initial training and during testing two days later, following an experimental night of sleep (n = 16, including high-density EEG recordings) or wakefulness (n = 17).

resultsOur results show sleep-dependent behavioral improvements correlated with sleep-spindle activity specifically over occipital cortices. Moreover, event-related potential (ERP) responses indicate a shift of attention away from predictable to unpredictable sequences after sleep, consistent with enhanced automaticity in the processing of predictable sequences.

conclusionsThese findings suggest a sleep-dependent improvement in the prediction of visual sequences, likely related to visual cortex reactivation during sleep spindles. Considering that controls in our experiments did not fully exclude oculomotor contributions, future studies will need to address the extent to which these effects depend on purely perceptual versus oculomotor sequence learning.

Indexed as

LearningSleepBrainElectroencephalographyHumansMalememorypredictionsequence learningsleepvisual perception

Identifiers

PMID33743012
PMCPMC8361350
OpenAlexW3136107328

What OpenQuestion holds

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LicenceCC BY-NC
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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.