Literature DB >> 27568805

Scalp and Source Power Topography in Sleepwalking and Sleep Terrors: A High-Density EEG Study.

Anna Castelnovo1,2, Brady A Riedner2, Richard F Smith2, Giulio Tononi2, Melanie Boly2, Ruth M Benca2.   

Abstract

STUDY
OBJECTIVES: To examine scalp and source power topography in sleep arousals disorders (SADs) using high-density EEG (hdEEG).
METHODS: Fifteen adult subjects with sleep arousal disorders (SADs) and 15 age- and gender-matched good sleeping healthy controls were recorded in a sleep laboratory setting using a 256 channel EEG system.
RESULTS: Scalp EEG analysis of all night NREM sleep revealed a localized decrease in slow wave activity (SWA) power (1-4 Hz) over centro-parietal regions relative to the rest of the brain in SADs compared to good sleeping healthy controls. Source modelling analysis of 5-minute segments taken from N3 during the first half of the night revealed that the local decrease in SWA power was prominent at the level of the cingulate, motor, and sensori-motor associative cortices. Similar patterns were also evident during REM sleep and wake. These differences in local sleep were present in the absence of any detectable clinical or electrophysiological sign of arousal.
CONCLUSIONS: Overall, results suggest the presence of local sleep differences in the brain of SADs patients during nights without clinical episodes. The persistence of similar topographical changes in local EEG power during REM sleep and wakefulness points to trait-like functional changes that cross the boundaries of NREM sleep. The regions identified by source imaging are consistent with the current neurophysiological understanding of SADs as a disorder caused by local arousals in motor and cingulate cortices. Persistent localized changes in neuronal excitability may predispose affected subjects to clinical episodes.
© 2016 Associated Professional Sleep Societies, LLC.

Entities:  

Keywords:  local sleep; night terrors; parasomnias; sleep arousal disorders; somnambulism

Mesh:

Year:  2016        PMID: 27568805      PMCID: PMC5020364          DOI: 10.5665/sleep.6162

Source DB:  PubMed          Journal:  Sleep        ISSN: 0161-8105            Impact factor:   5.849


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