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NREM sleep instability in children with sleep terrors: the role of slow wave activity interruptions
Oliviero Bruni1, Raffaele Ferri, Luana Novelli
1Center for Pediatric Sleep Disorders, Department of Developmental Neurology and Psychiatry, University of Rome La Sapienza, Via dei Sabelli 108, 00185 Rome, Italy. oliviero.bruni@uniroma1.it
Insights
Children with sleep terrors (ST) exhibit increased NREM sleep instability, specifically faster EEG alternations during slow-wave sleep (SWS). This cyclic alternating pattern (CAP) variation may serve as a neurophysiological marker for arousal disorders.
Area of Science:
- Neuroscience
- Sleep Medicine
- Pediatrics
Background:
- Sleep terrors (ST) are common pediatric parasomnias.
- The cyclic alternating pattern (CAP) reflects NREM sleep instability.
- NREM sleep instability in ST is not well understood.
Purpose of the Study:
- To compare NREM sleep instability using CAP in children with ST versus controls.
- To identify potential neurophysiological markers for ST.
Main Methods:
- 10 boys with ST and 11 age-matched controls underwent polysomnography.
- Sleep macrostructure and CAP were visually scored.
- CAP parameters, including A1 index and phase durations in SWS, were analyzed.
Main Results:
- Children with ST had more awakenings and lower sleep efficiency.
- ST subjects showed increased total CAP rate and A1 index in SWS.
- Faster CAP alternations (shorter intervals) were observed in SWS for ST patients.
Conclusions:
- Children with ST demonstrate abnormal EEG amplitude alternations during SWS.
- This instability, marked by CAP, may be a neurophysiological marker for ST and other arousal disorders.
Objective:
To evaluate NREM sleep instability, as measured by the cyclic alternating pattern (CAP), in children with sleep terrors (ST) vs. normal controls.
Methods:
Ten boys (mean age: 8.5 years, range 5-13) meeting the following inclusion criteria: (a) complaint of ST several times a month, (b) a history of ST confirmed by a third person, and (c) a diagnosis of ST according to the ICSD-2 criteria. Eleven age-matched control children with parental report of at least 8.5h of nightly sleep, absence of known daytime consequences of sleep disorders were recruited by advertisement from the community. Sleep was visually scored for sleep macrostructure and CAP using standard criteria.
Results:
Sleep macrostructure showed only a significantly increased number of awakenings per hour and reduced sleep efficiency in ST subjects. CAP parameters analysis revealed several significant differences in ST vs. controls: an increase of total CAP rate in SWS, of A1 index in SWS and of the mean duration of A phases while B phases had a decreased duration, exclusively in SWS. The normalized CAP interval-distribution graphs showed significant differences in SWS with interval classes 10< or = i < 35s higher in children with ST and intervals classes above 50s higher in normal controls.
Conclusions:
Children with ST showed faster alternations of the amplitude of slow EEG bursts during SWS. This abnormally fast alternation of the EEG amplitude in SWS is linked to the frequent intrusion of CAP B phases interrupting the continuity of slow delta activity and could be considered as a neurophysiological marker of ST.
Significance:
This abnormal alternation of the EEG amplitude in SWS is associated with the occurrence of parasomnias and might be considered as a neurophysiological marker of disorders of arousal.
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