Sleep spindle maturation enhances slow oscillation-spindle coupling
Ann‐Kathrin JoechneriD, Michael A HahniD, Georg Gruber, Kerstin HoedlmoseriD, Markus Werkle‐BergneriD
Abstract
The synchronization of canonical fast sleep spindle activity (12.5-16 Hz) precisely during the slow oscillation up peak is considered an essential feature of adult non-rapid eye movement sleep. However, there is little knowledge on how this well-known coalescence between slow oscillations and sleep spindles develops. Leveraging individualized detection of single events, we first provide a detailed cross-sectional characterization of age-specific patterns of slow and fast sleep spindles, slow oscillations, and their coupling in children aged 5 to 6, 8 to 11, and 14 to 18 years. Critically, based on this, we then investigated how spindle and slow oscillation maturity substantiate age differences in their precise orchestration. While the predominant type of fast spindles was development-specific in that it was still nested in a frequency range below the canonical fast spindle range for the majority of children, the well-known slow oscillation-spindle coupling pattern was evident for sleep spindles in the canonical (adult-like) fast spindle range in all three age groups - but notably less precise in children. To corroborate these findings, we linked personalized measures of fast spindle maturity, which indicate the similarity between the prevailing development-specific and adult-like fast spindles, and slow oscillation maturity, which reflects the extent to which slow oscillations show frontal dominance, with individual slow oscillation-spindle coupling patterns. Importantly, we found that fast spindle maturity was uniquely associated with enhanced slow oscillation-spindle coupling strength and precision. Taken together, our results suggest that the increasing ability to generate canonical fast sleep spindles actuates precise slow oscillation-spindle coupling patterns across child and adolescent development.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 17
- FWCI
- 2.54
- Field percentile
- top 10%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- From co-occurrence to increasingly precise temporal coordination: Development of slow oscillation-spindle coupling from infancy to toddlerhood
Eva‐Maria Kurz, Matthias Moelle, … Manuela Friedrich·bioRxiv·Sep 3, 2026
- The adolescent pattern of sleep spindle development revealed by HD-EEG polysomnography
Gábor Bocskai, Adrián Pótári, … Ilona Kovács·bioRxiv·Dec 20, 2021
- Slow oscillation-spindle coupling strength predicts real-life gross-motor learning in adolescents and adults
Michael A Hahn, Kathrin Bothe, … Kerstin Hoedlmoser·eLifePeer-reviewed·Feb 7, 2022
- Phase precession of spindle-slow oscillation coupling across the human brain
Alex C. Bender, Madeline Taubkin, … Alice D. Lam·bioRxiv·Nov 20, 2025
- Topographical relocation of adolescent sleep spindles reveals a new maturational pattern of the human brain
Ferenc Gombos, Róbert Bódizs, … Ilona Kovács·Scientific ReportsPeer-reviewed·Apr 29, 2022
- Precise Slow Oscillation-Spindle Coupling Promotes Memory Consolidation in Younger and Older Adults
Beate E. Muehlroth, Myriam C. Sander, … Markus Werkle‐Bergner·Scientific ReportsPeer-reviewed·Feb 13, 2019