Sleep in children with autistic spectrum disorder: a questionnaire and polysomnographic study

Silvia Miano1, Oliviero Bruni, Maurizio Elia

  • 1Department of Neurology, Sleep Research Centre, Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS), Via C. Ruggero 73, 94018 Troina, Italy.

Sleep Medicine
|August 31, 2007
PubMed

Insights

Children with autism spectrum disorder (ASD) experience more sleep problems, including difficulty falling asleep and daytime sleepiness. Polysomnography revealed subtle NREM sleep alterations, particularly reduced cyclic alternating pattern (CAP) A1 subtypes during slow-wave sleep (SWS).

Area of Science:

  • Neuroscience
  • Developmental Psychology
  • Sleep Medicine

Background:

  • Autistic spectrum disorder (ASD) is a neurodevelopmental condition often associated with sleep disturbances.
  • Understanding sleep patterns in ASD is crucial for improving quality of life and cognitive function.

Purpose of the Study:

  • To comprehensively evaluate sleep in children with ASD using questionnaires and polysomnography.
  • To analyze the cyclic alternating pattern (CAP) during sleep in ASD.

Main Methods:

  • Thirty-one children with ASD and age-matched controls underwent sleep evaluation.
  • Methods included a 45-item sleep questionnaire and overnight polysomnography in a sleep laboratory.

Main Results:

  • Questionnaires indicated high rates of sleep-onset difficulties, enuresis, and daytime sleepiness in ASD children.
  • Polysomnography revealed reduced total sleep time, REM latency, and a lower CAP rate during slow-wave sleep (SWS) in ASD subjects.
  • A lower percentage of A1 subtypes during SWS was observed in ASD children compared to controls.

Conclusions:

  • While questionnaires highlighted significant sleep issues in ASD, sleep staging provided partial confirmation.
  • Cyclic alternating pattern (CAP) analysis revealed subtle NREM sleep alterations in ASD.
  • Reduced CAP A1 subtypes during SWS may impact cognitive functioning in children with ASD.
Abstract