The Space–Time Organisation of Sleep Slow Oscillations as Potential Biomarker for Hypersomnolence

Research suggests that the spatial profile of slow wave activity (SWA) could be altered in hypersomnolence. Slow oscillations (SOs; 0.5-1.5 Hz), single waveform events contributing to SWA, can be labelled as Global, Frontal, or Local depending on their presentation on the scalp. We showed that SO space-time types differentiate in their amplitudes, coordination with sleep spindles, and propagation patterns. This study applies our data-driven analysis to the nocturnal sleep of adults with and without hypersomnolence and major depressive disorder (MDD) to explore the potential relevance of SO space-time patterns as hypersomnolence signatures in the sleep EEG. We leverage an existing dataset of nocturnal polysomnography with high-density EEG in 83 adults, organised in four groups depending on the presence/absence of hypersomnolence and on the presence/absence of MDD. Group comparisons were conducted considering either two groups (hypersomnolence status) or the four groups separately. Data shows enhanced Frontal SO activity compared with Global activity in hypersomnolence, with or without MDD, and a loss of Global SO amplitude at central regions in hypersomnolence without MDD compared to controls. As Global SOs travel fronto-parietally, we interpret these results as likely driven by a loss of coordination of Global SO activity in hypersomnolence without MDD, resulting in an overabundance of Frontal SOs. This study suggests that characteristics of Frontal SO and Global SOs may have the potential to differentiate individuals with hypersomnolence without MDD, and that the space-time organisation of SOs could be a mechanistically relevant indicator of changes in sleep brain dynamics related to hypersomnolence.

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Publication Details

Journal
Journal of Sleep Research
Published
2025-04-01
DOI
https://doi.org/10.1111/jsr.70059
Citations
2
Primary Topic
Sleep and Wakefulness Research
Type
article
Field-Weighted Citation Impact
2.86

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article

The Space–Time Organisation of Sleep Slow Oscillations as Potential Biomarker for Hypersomnolence

Paola Malerba, Sara C. Mednick, David Thomas Plante, Mahmoud Alipour et al.
2 citations
Journal of Sleep Research
Sleep and Wakefulness Research
2.86
article

The Space–Time Organisation of Sleep Slow Oscillations as Potential Biomarker for Hypersomnolence

Paola Malerba, Sara C. Mednick, David Thomas Plante, Mahmoud Alipour, Jesse David Cook, Joseph R. Rausch
article en
2 citations

Abstract

Research suggests that the spatial profile of slow wave activity (SWA) could be altered in hypersomnolence. Slow oscillations (SOs; 0.5-1.5 Hz), single waveform events contributing to SWA, can be labelled as Global, Frontal, or Local depending on their presentation on the scalp. We showed that SO space-time types differentiate in their amplitudes, coordination with sleep spindles, and propagation patterns. This study applies our data-driven analysis to the nocturnal sleep of adults with and without hypersomnolence and major depressive disorder (MDD) to explore the potential relevance of SO space-time patterns as hypersomnolence signatures in the sleep EEG. We leverage an existing dataset of nocturnal polysomnography with high-density EEG in 83 adults, organised in four groups depending on the presence/absence of hypersomnolence and on the presence/absence of MDD. Group comparisons were conducted considering either two groups (hypersomnolence status) or the four groups separately. Data shows enhanced Frontal SO activity compared with Global activity in hypersomnolence, with or without MDD, and a loss of Global SO amplitude at central regions in hypersomnolence without MDD compared to controls. As Global SOs travel fronto-parietally, we interpret these results as likely driven by a loss of coordination of Global SO activity in hypersomnolence without MDD, resulting in an overabundance of Frontal SOs. This study suggests that characteristics of Frontal SO and Global SOs may have the potential to differentiate individuals with hypersomnolence without MDD, and that the space-time organisation of SOs could be a mechanistically relevant indicator of changes in sleep brain dynamics related to hypersomnolence.

Journal of Sleep ResearchVol. 34(5)
Nationwide Children's Hospital (US), University of Wisconsin–Madison (US), University of California, Irvine (US), The Ohio State University (US)
National Heart, Lung, and Blood Institute, National Institute of Mental Health
Openalex Percentile: Top 11%
Sleep and Wakefulness Research
2.86
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