News Release

Two new tools to enhance effectiveness of behavioral therapy in children with autism

Papers published in 2 leading journals describe which autism patients will benefit from pivotal response treatment and a potential new treatment for those that won't

Peer-Reviewed Publication

George Washington University

Brain Response Predicts Treatment Outcome in Young Children with ASD

image: Using fMRI, researchers identified four distinct brain regions (left column) in 20 children with ASD who were shown images containing biological vs. scrambled motion before treatment. When their brain responses were higher in these regions, they were more able to respond positively to PRT. The scatterplots (right column) indicate that children who responded more strongly to biological motion initially tend to show more of a decrease in the severity of their ASD symptoms after PRT, suggesting that the treatment was more beneficial. view more 

Credit: Daniel Yang

WASHINGTON (Nov, 15, 2016)--In two scientific papers published Tuesday, researchers identified two approaches that have the potential to help a large number of children with autism spectrum disorder through behavioral therapy.

The first paper, "Brain Responses to Biological Motion Predict Treatment Outcome in Young Children with Autism," found that functional MRIs (fMRI) could predict which children will benefit from Pivotal Response Treatment (PRT), one of a few evidence-based interventions for the condition, with near-perfect accuracy.

Researchers from the George Washington University and the Children's National Health System used fMRI to determine the functionality of four clusters in the brain that are involved in processing emotional information, social information, social attention and social reward. According to the study, children with higher functionality in those brain clusters benefitted more from PRT.

The behavioral therapy is currently effective in approximately 60 percent of children and is costly and time-intensive. Functional MRI could be used to identify the children most likely to respond to the treatment and may lead to follow-up research to better prepare those who would not.

"Parents want their children to receive the best treatment during this period, but it is not always clear how much a given treatment plan would benefit the children," said Daniel Yang, researcher at the GW Autism & Neurodevelopmental Disorders Institute, assistant research professor of pediatrics at the GW School of Medicine and Health Sciences and Children's National, and one of the lead authors of the paper. "Although more research is needed, the current research provides an important first step toward establishing objective biomarkers that can accurately predict treatment outcome in young children with autism."

The second paper, "Intranasal Oxytocin Enhances Connectivity in the Neural Circuitry Supporting Social Motivation and Social Perception in Children with Autism," examined the effect of the hormone oxytocin on the activity of social perception and reward brain circuits in children with autism spectrum disorder. This was one of the first investigations of its kind.

Researchers found that by administering oxytocin as a nasal spray before social experiences, children had stronger responses to the social information. The findings suggest that use of oxytocin treatment before behavioral therapy could help reinforce the reward system in the brain that motivates social behaviors. However, researchers stress that the treatment must be developed in conjunction with therapies designed to positively reward social behaviors, as heightened response to negative emotions can also occur.

"Although oxytocin is often referred to as the 'love' hormone, its effects actually depend on a child's social surroundings," said Allison Jack, assistant research professor of pharmacology and physiology at the GW School of Medicine and Health Sciences and a co-author of the paper. "Our study demonstrates that administering oxytocin to children with autism spectrum disorders has different effects on their brains depending on what type of environment they are exposed to. Only when children were experiencing positive social cues (like happy voices) did we see oxytocin having the effect that we would need it to have for therapeutic use, by increasing brain activity in the reward system."

While the researchers said the results are promising, they do not suggest that using intranasal oxytocin should be considered as a core treatment for autism. Rather, the oxytocin treatment could be a way to enhance behavioral methods that are specifically tailored to provide positive social experiences and rewards.

The sample sizes of both studies were small, but the results were striking. The findings have the potential to complement each other, according to one of the corresponding authors.

"This research moves us closer to our goal of developing precision treatments for people with autism--getting the right treatment to the right person at the best time," said Kevin Pelphrey, Carbonell Family Professor in Autism and Neurodevelopmental Disorders, director of the GW Autism and Neurodevelopmental Disorders Institute, a collaboration between GW and Children's National, and a co-author of both papers. "As we move forward from here, we will launch a new era--brain imaging will become a routine part of a translational research chain. Brain imaging biological markers could be used, at the outset, to make treatment decisions related to dose, duration, intensity and specific behavioral treatment approaches, as well as decisions about which drugs to use to improve treatment response."

Dr. Pelphrey is also professor of pharmacology and physiology at the GW School of Medicine and Health Sciences.

The papers were published Nov. 15 in Translational Psychiatry and Scientific Reports, respectively.

In April, Dr. Pelphrey published a paper identifying a first-of-its kind approach to using brain imaging to enhance diagnosis, improve treatment and track progress of boys with autism.

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MEDIA CONTACTS:
Emily Grebenstein: emgreb@gwu.edu, 202-994-3087
Kurie Fitzgerald: kfitzgerald@gwu.edu, 202-994-6461


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