"EEGs are low-cost, non-invasive and relatively easy to incorporate into well-baby checkups," says Charles Nelson, PhD, director of the Laboratories of Cognitive Neuroscience at Boston Children's Hospital and co-author of the study. "Their reliability in predicting whether a child will develop
raises the possibility of intervening very early, well before clear behavioral symptoms emerge. This could lead to better outcomes and perhaps even prevent some of the behaviors associated with ASD."
‘Low-cost and non-invasive EEGs can accurately predict or rule out autism spectrum disorder (ASD) in infants.’
The study analyzed data from the Infant Sibling Project (now called the Infant Screening Project), a collaboration between Boston Children's Hospital and Boston University that seeks to map early development and identify infants at risk for developing ASD and/or language and communication difficulties.
William Bosl, PhD, associate professor of Health Informatics and Clinical Psychology at the University of San Francisco, also affiliated with the Computational Health Informatics Program (CHIP) at Boston Children's Hospital, has been working for close to a decade on algorithms to interpret EEG signals, the familiar squiggly lines generated by electrical activity in the brain. Bosl's research suggests that even an EEG that appears normal contains "deep" data that reflect brain function, connectivity patterns and structure that can be found only with computer algorithms.
The Infant Screening Project provided Bosl with EEG data from 99 infants considered at high risk for ASD (having an older sibling with the diagnosis) and 89 low-risk controls (without an affected sibling). The EEGs were taken at 3, 6, 9, 12, 18, 24 and 36 months of age by fitting a net over the babies' scalps with 128 sensors as the babies sat in their mothers' laps. (An experimenter blew bubbles to distract them.) All babies also underwent extensive behavioral evaluations with the Autism Diagnostic Observation Schedule (ADOS), an established clinical diagnostic tool.
Bosl's computational algorithms analyzed six different components (frequencies) of the EEG (high gamma, gamma, beta, alpha, theta, delta), using a variety of measures of signal complexity. These measures can reflect differences in how the brain is wired and how it processes and integrates information, says Bosl.
The algorithms predicted a clinical diagnosis of ASD with high specificity, sensitivity and positive predictive value, exceeding 95 percent at some ages.
"The results were stunning," Bosl says. "Our predictive accuracy by 9 months of age was nearly 100 percent. We were also able to predict ASD severity, as indicated by the ADOS Calibrated Severity Score, with quite high reliability, also by 9 months of age."
Bosl believes that the early differences in signal complexity, drawing upon multiple aspects of brain activity, fit with the view that autism is a disorder that begins during the brain's early development but can take different trajectories. In other words, an early predisposition to autism may be influenced by other factors along the way.
"We believe that infants who have an older sibling with autism may carry a genetic liability for developing autism," says Nelson. "This increased risk, perhaps interacting with another genetic or environmental factor, leads some infants to develop autism -- although clearly not all, since we know that four of five "infant sibs" do not develop autism."