Alterations in aperiodic and periodic EEG activity in young children with Down syndrome

McKena Geiger1, Sophie R Hurewitz1, Katherine Pawlowski1

  • 1Division of Developmental Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.

Neurobiology of Disease
|August 22, 2024
PubMed

Insights

Electroencephalography (EEG) in young children with Down syndrome (DS) reveals distinct brain activity patterns. These findings offer insights into the neurobiology of intellectual disability in DS, independent of cognitive delays.

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Genetics

Background:

  • Down syndrome (DS) is the leading genetic cause of intellectual disability.
  • Neurobiological underpinnings of cognitive impairments in DS remain poorly understood.
  • Limited electroencephalographic (EEG) research exists for young children with DS.

Purpose of the Study:

  • To investigate resting-state EEG features in toddlers and preschoolers with DS.
  • To compare EEG characteristics between children with DS and matched control groups.
  • To explore neurobiological differences associated with DS in early development.

Main Methods:

  • Analysis of resting-state EEG data from 29 toddlers/preschoolers with DS (13-48 months).
  • Comparison of aperiodic and periodic EEG features with age-matched (n=29) and developmental-matched (n=58) controls.
  • Assessment of EEG spectral properties, including slope, theta power, and alpha peak amplitude.

Main Results:

  • Children with DS showed a significantly reduced aperiodic slope and increased theta power.
  • A decrease in alpha peak amplitude was observed in the DS group.
  • A majority of DS participants exhibited a prominent theta peak, absent in age-matched controls, suggesting intrinsic neurophysiological differences.

Conclusions:

  • Distinct EEG signatures, including altered theta and alpha activity, are present in young children with Down syndrome.
  • These neurophysiological differences appear independent of general cognitive development delays.
  • Findings contribute to understanding the neurobiology of intellectual disability in DS during early development.