Evidence map›Paper›PMID 35487959›Full record

ArticleScientific reports2022

Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain.

Ferenc Gombos, Róbert Bódizs, Adrián Pótári, Gábor Bocskai, Andrea Berencsi, Hanna Szakács, Ilona Kovács

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. 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
1.1field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Ferenc Gombos *Laboratory for Psychological Research, Pázmány Péter Catholic University, 1 Mikszáth Kálmán Sq., Budapest, 1088, Hungary.
Róbert Bódizs *Institute of Behavioural Sciences, Semmelweis University, Budapest, 1089, Hungary.
Adrián PótáriAdolescent Development Research Group, Hungarian Academy of Sciences - Pázmány Péter Catholic University, Budapest, 1088, Hungary.
Gábor BocskaiLaboratory for Psychological Research, Pázmány Péter Catholic University, 1 Mikszáth Kálmán Sq., Budapest, 1088, Hungary.
Andrea BerencsiAdolescent Development Research Group, Hungarian Academy of Sciences - Pázmány Péter Catholic University, Budapest, 1088, Hungary.
Hanna SzakácsLaboratory for Psychological Research, Pázmány Péter Catholic University, 1 Mikszáth Kálmán Sq., Budapest, 1088, Hungary.
Ilona KovácsLaboratory for Psychological Research, Pázmány Péter Catholic University, 1 Mikszáth Kálmán Sq., Budapest, 1088, Hungary. dr.ilona.kovacs@gmail.com.
Pázmány Péter Catholic University · HUOrszágos Idegsebészeti Tudományos Intézet · HUSemmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current theories of human neural development emphasize the posterior-to-anterior pattern of brain maturation. However, this scenario leaves out significant brain areas not directly involved with sensory input and behavioral control. Suggesting the relevance of cortical activity unrelated to sensory stimulation, such as sleep, we investigated adolescent transformations in the topography of sleep spindles. Sleep spindles are known to be involved in neural plasticity and in adults have a bimodal topography: slow spindles are frontally dominant, while fast spindles have a parietal/precuneal origin. The late functional segregation of the precuneus from the frontoparietal network during adolescence suggests that spindle topography might approach the adult state relatively late in development, and it may not be a result of the posterior-to-anterior maturational pattern. We analyzed the topographical distribution of spindle parameters in HD-EEG polysomnographic sleep recordings of adolescents and found that slow spindle duration maxima traveled from central to anterior brain regions, while fast spindle density, amplitude and frequency peaks traveled from central to more posterior brain regions. These results provide evidence for the gradual posteriorization of the anatomical localization of fast sleep spindles during adolescence and indicate the existence of an anterior-to-posterior pattern of human brain maturation.

Indexed as

SleepSleep StagesAdolescentAdultBrainElectroencephalographyHumansParietal Lobe

Identifiers

PMID35487959
PMCPMC9054798
OpenAlexW4225254243

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LicenceCC BY
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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.