Evidence map›Paper›PMID 42310467›Full record

ArticleScientific reports2026

The infraslow fluctuation of sigma power during sleep and its links to markers of arousal and memory reactivation across development.

Maria E Dimitriades, Alejandro Osorio-Forero, Sara Fattinger, Simone von Arx, Salome Kurth, Fiona Pugin, Valeria Jaramillo, Carina Volk, Elena Krugliakova, Melanie Furrer and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 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
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  3. 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

14 authors.

Maria E DimitriadesChild Development Center, University Children's Hospital Zurich, Zurich, Switzerland.
Alejandro Osorio-ForeroNetherlands Institute for Neuroscience, Department of Sleep and Cognition, Amsterdam, Netherlands.
Sara FattingerChild Development Center, University Children's Hospital Zurich, Zurich, Switzerland.
Simone von ArxChild Development Center, University Children's Hospital Zurich, Zurich, Switzerland.
Salome KurthCenter of Competence Sleep & Health Zurich, University of Zurich, Zurich, Switzerland.
Fiona PuginEudox Statistische Beratung, Basel, 4031, Switzerland.
Valeria JaramilloChild Development Center, University Children's Hospital Zurich, Zurich, Switzerland.
Carina VolkChildren's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
Elena KrugliakovaChild Development Center, University Children's Hospital Zurich, Zurich, Switzerland.
Melanie FurrerChild Development Center, University Children's Hospital Zurich, Zurich, Switzerland.
Sven LeachChild Development Center, University Children's Hospital Zurich, Zurich, Switzerland.
Peter AchermannInstitute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.
Miriam Gerstenberg *Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
Reto Huber *Child Development Center, University Children's Hospital Zurich, Zurich, Switzerland. reto.huber@kispi.uzh.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sleep is both a state of disconnection from the environment and a critical period for restoration. But how does sleep balance responsiveness with the protection of key functions? The infraslow fluctuation of sigma power (ISFS)-the clustering of sleep spindles over 10-100 s-is thought to regulate this trade-off in rodents by alternating between fragile periods of high arousability and protected periods of spindle-rich stability. However, the organization of arousal and memory reactivation markers within the human ISFS and its conservation in younger ages remain unclear. This study characterizes the ISFS from childhood to young adulthood (N = 154; ages 8-26), examining its relationship with electrophysiological markers of arousal (i.e., microarousals) and memory reactivation (i.e., slow wave-sleep spindle coupling). Results indicate that the ISFS is present across all ages, with frequency, variability, and strength increasing from early to late adolescence. Notably, electrophysiological markers of arousal and memory reactivation are organized within the spindle-rich ISFS peak. The consistent presence and organization of the ISFS suggest it may be intrinsic to sleep, with adolescence marking a dynamic window. These insights may guide interventions to promote healthier sleep across development.

Indexed as

ArousalMemorySleepAdolescentAdultChildElectroencephalographyFemaleHumansMaleYoung AdultArousalDevelopmenthigh-density EEGInfraslowMemorySleepSleep Spindles

Identifiers

PMID42310467
PMCPMC13542187

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.