EEG power at 3 months in infants at high familial risk for autism

April R Levin1,2,3, Kandice J Varcin4,5, Heather M O'Leary6

  • 1Boston Children's Hospital, 300 Longwood Avenue, BCH 3213, Boston, MA, 02115, USA. april.levin@childrens.harvard.edu.

Insights

Infants at high familial risk for autism show reduced frontal electroencephalographic (EEG) power by 3 months. This early brain activity difference predicts poorer expressive language development by 12 months.

Area of Science:

  • Neurodevelopmental disorders
  • Infant brain development
  • Autism spectrum disorder (ASD) research

Background:

  • Infant brain development alterations may precede developmental disorder diagnosis.
  • Infants at high risk for autism also face increased risk for language disorders.
  • Early identification of neurodevelopmental trajectories is crucial.

Purpose of the Study:

  • To assess electroencephalographic (EEG) differences in 3-month-old infants at high versus low familial risk for autism.
  • To determine the predictive significance of 3-month EEG power for later developmental outcomes.

Main Methods:

  • Prospective, longitudinal study of infant siblings of children with autism (high risk) and typically developing children (low risk).
  • EEG data acquired at 3 months; developmental assessments conducted from 6 to 36 months.
  • Statistical analysis of relationships between 3-month frontal EEG power and later developmental outcomes, including autism diagnosis and language development.

Main Results:

  • Infants at high familial risk for autism exhibited reduced frontal EEG power across several frequency bands at 3 months compared to low-risk infants.
  • Reduced frontal high-alpha power at 3 months was significantly associated with poorer expressive language skills at 12 months.

Conclusions:

  • Reduced frontal EEG power in early infancy may signal an elevated risk for impaired expressive language development.
  • These findings support the concept of reduced power as a potential biomarker for atypical brain function in infants at risk for autism.
  • Altered developmental trajectories in infants at familial risk for autism extend beyond autism-specific domains.
Abstract

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