Evidence map›Paper›PMID 32541070›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2020

Integrity of Corpus Callosum Is Essential for theCross-Hemispheric Propagation of Sleep Slow Waves:A High-Density EEG Study in Split-Brain Patients.

Giulia Avvenuti, Giacomo Handjaras, Monica Betta, Jacinthe Cataldi, Laura Sophie Imperatori, Simona Lattanzi, Brady A Riedner, Pietro Pietrini, Emiliano Ricciardi, Giulio Tononi and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 53 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Sleep loss induces cholesterol-associated myelin dysfunction.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  8. Article
  9. Illuminating consciousness.Frontiers in psychology · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. Photosensitivity of an aging brain.bioRxiv : the preprint server for biology · 2025
    Article
  14. Article
  15. Thalamic involvement defines distinct slow-wave subtypes in NREM sleep.bioRxiv : the preprint server for biology · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Sleep disorders in pediatric patients with agenesis of the corpus callosum.Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2024
    Article
  20. 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

16 authors at 4 institutions in 4 countries.

Giulia AvvenutiMolecular Mind Laboratory Research Unit, IMT School for Advanced Studies, 55100 Lucca, Italy.ORCID 0000-0002-9031-1632
Giacomo HandjarasMolecular Mind Laboratory Research Unit, IMT School for Advanced Studies, 55100 Lucca, Italy.
Monica BettaMolecular Mind Laboratory Research Unit, IMT School for Advanced Studies, 55100 Lucca, Italy.ORCID 0000-0002-5672-1638
Jacinthe CataldiCenter for Investigation and Research on Sleep, Lausanne University Hospital, CH-1011 Lausanne, Switzerland.
Laura Sophie ImperatoriMolecular Mind Laboratory Research Unit, IMT School for Advanced Studies, 55100 Lucca, Italy.
Simona LattanziDepartment of Experimental and Clinical Medicine, Marche Polytechnic University, 60121 Ancona, Italy.
Brady A RiednerDepartment of Psychiatry, University of Madison, Madison, Wisconsin 53706.
Pietro PietriniMolecular Mind Laboratory Research Unit, IMT School for Advanced Studies, 55100 Lucca, Italy.ORCID 0000-0002-6768-5556
Emiliano RicciardiMolecular Mind Laboratory Research Unit, IMT School for Advanced Studies, 55100 Lucca, Italy.ORCID 0000-0002-7178-9534
Giulio TononiDepartment of Psychiatry, University of Madison, Madison, Wisconsin 53706.ORCID 0000-0002-3892-4087
Francesca SiclariCenter for Investigation and Research on Sleep, Lausanne University Hospital, CH-1011 Lausanne, Switzerland.
Gabriele PolonaraDepartment of Odontostomatologic and Specialized Clinical Sciences, Marche Polytechnic University, 60121 Ancona, Italy.
Mara FabriDepartment of Experimental and Clinical Medicine, Marche Polytechnic University, 60121 Ancona, Italy.
Mauro SilvestriniDepartment of Experimental and Clinical Medicine, Marche Polytechnic University, 60121 Ancona, Italy.
Michele BellesiDepartment of Experimental and Clinical Medicine, Marche Polytechnic University, 60121 Ancona, Italy giulio.bernardi@imtlucca.it michele.bellesi@bristol.ac.uk.
Giulio BernardiMolecular Mind Laboratory Research Unit, IMT School for Advanced Studies, 55100 Lucca, Italy giulio.bernardi@imtlucca.it michele.bellesi@bristol.ac.uk.ORCID 0000-0003-4045-7075
IMT School for Advanced Studies Lucca · ITMarche Polytechnic University · ITUniversity of Lausanne · CHUniversity of Wisconsin–Madison · US

Funding

Wellcome TrustWellcome Trust 215267/Z/19/Z
6 · The paper itself

Abstract

The slow waves of non-rapid eye movement (NREM) sleep reflect experience-dependent plasticity and play a direct role in the restorative functions of sleep. Importantly, slow waves behave as traveling waves, and their propagation is assumed to occur through cortico-cortical white matter connections. In this light, the corpus callosum (CC) may represent the main responsible for cross-hemispheric slow-wave propagation. To verify this hypothesis, we performed overnight high-density (hd)-EEG recordings in five patients who underwent total callosotomy due to drug-resistant epilepsy (CPs; two females), in three noncallosotomized neurologic patients (NPs; two females), and in a sample of 24 healthy adult subjects (HSs; 13 females). In all CPs slow waves displayed a significantly reduced probability of cross-hemispheric propagation and a stronger inter-hemispheric asymmetry. In both CPs and HSs, the incidence of large slow waves within individual NREM epochs tended to differ across hemispheres, with a relative overall predominance of the right over the left hemisphere. The absolute magnitude of this asymmetry was greater in CPs relative to HSs. However, the CC resection had no significant effects on the distribution of slow-wave origin probability across hemispheres. The present results indicate that CC integrity is essential for the cross-hemispheric traveling of slow waves in human sleep, which is in line with the assumption of a direct relationship between white matter integrity and slow-wave propagation. Our findings also revealed a residual cross-hemispheric slow-wave propagation that may rely on alternative pathways, including cortico-subcortico-cortical loops. Finally, these data indicate that the lack of the CC does not lead to differences in slow-wave generation across brain hemispheres.

Indexed as

Brain WavesSleep, Slow-WaveAdultAgedCorpus CallosumElectroencephalographyFemaleHumansMaleMiddle AgedSplit-Brain Procedureconnectivitycorpus callosumNREMsleepslow wave

Identifiers

PMID32541070
PMCPMC7363462
OpenAlexW3017831443

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.