Sleep and EEG features of newborns with 18 and 13 trisomy syndromes

Brain & Development
|January 1, 1979
PubMed

Insights

Newborns with trisomy 18 syndrome exhibit poor sleep patterns, including prolonged wakefulness and difficulty organizing sleep cycles. Sleep profiles show some normalization over time but retain unique EEG characteristics.

Area of Science:

  • Neonatal Neurology
  • Developmental Pediatrics
  • Clinical Genetics

Background:

  • Trisomy 18 (Edwards syndrome) and Trisomy 13 (Patau syndrome) are severe chromosomal abnormalities affecting newborns.
  • Sleep disturbances are common in infants with genetic syndromes, impacting development and health.
  • Understanding sleep patterns in these conditions is crucial for clinical management.

Purpose of the Study:

  • To characterize the sleep patterns of newborns with Trisomy 18 and Trisomy 13 syndromes.
  • To investigate the organization and electroencephalographic (EEG) features of sleep in these infants.
  • To assess the temporal changes in sleep cyclicity during the neonatal period.

Main Methods:

  • Serial polygraphic recordings (2-3 hours) were performed on five full-term newborns with Trisomy 18 and one with Trisomy 13.
  • Sleep states and EEG patterns were analyzed, focusing on sleep cycle organization and specific sleep features.
  • Recordings were evaluated during the immediate neonatal period and after 1-2 weeks.

Main Results:

  • Newborns with Trisomy 18 showed poor sleep, with extended wakefulness/drowsiness and difficulties organizing stable sleep cycles.
  • No consistent sleep profile abnormalities were uniquely characteristic of Trisomy 18 or 13.
  • EEG patterns showed poor correlation with sleep states; trace alternant patterns increased, and high-voltage slow patterns decreased in quiet sleep over time.

Conclusions:

  • Infants with Trisomy 18 syndrome experience significant sleep organization challenges in the neonatal period.
  • While some normalization of sleep cyclicity occurs, persistent EEG abnormalities are noted even at later conceptional ages.
  • Further research is needed to understand the long-term implications of these sleep disturbances for development in Trisomy 18 and 13.