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Restricted and Repetitive Behavior and Brain Functional Connectivity in Infants at Risk for Developing Autism
Claire J McKinnon1, Adam T Eggebrecht2, Alexandre Todorov3
1Department of Psychiatry, Washington University School of Medicine, St. Louis, Missouri; Biological Sciences Division, University of Chicago, Chicago, Illinois.
Insights
This study reveals the earliest brain network differences linked to restricted and repetitive behaviors (RRBs) in infants at high risk for autism spectrum disorder (ASD). Findings highlight specific neural substrates for potential early interventions.
Area of Science:
- Neuroscience
- Developmental Psychology
- Pediatrics
Background:
- Restricted and repetitive behaviors (RRBs) are early behavioral markers for autism spectrum disorder (ASD).
- The underlying brain function for RRBs in infants remains largely unknown.
- Understanding these early markers is crucial for timely diagnosis and intervention.
Purpose of the Study:
- To identify functional brain networks associated with the development of RRB subcategories in infants.
- To investigate the emergence of RRBs in relation to brain function in high-risk infants.
- To provide insights into the neural substrates of early ASD behavioral markers.
Main Methods:
- Collected resting-state functional connectivity (fc) MRI data from 167 high- and low-familial-risk infants at 12 and 24 months.
- Categorized RRBs into four subcategories: restricted, stereotyped, ritualistic/sameness, and self-injurious.
- Employed a data-driven approach to link RRB subcategories with functional brain network connectivity.
Main Results:
- Ritualistic/sameness behavior correlated with altered connectivity between visual and control/default mode networks.
- Stereotyped and restricted behaviors at 24 months showed associations with connectivity in default mode, control, dorsal attention, and subcortical networks.
- No significant network associations were found for self-injurious behavior.
Conclusions:
- This study provides the earliest description of functional brain systems underlying RRBs in infants.
- Findings reinforce the validity of RRB subcategories and suggest specific neural targets for future interventions.
- The identified neural correlates of RRBs may inform early diagnostic and therapeutic strategies for ASD.
Background:
Restricted and repetitive behaviors (RRBs), detectable by 12 months in many infants in whom autism spectrum disorder (ASD) is later diagnosed, may represent some of the earliest behavioral markers of ASD. However, brain function underlying the emergence of these key behaviors remains unknown.
Methods:
Behavioral and resting-state functional connectivity (fc) magnetic resonance imaging data were collected from 167 children at high and low familial risk for ASD at 12 and 24 months (n = 38 at both time points). Twenty infants met criteria for ASD at 24 months. We divided RRBs into four subcategories (restricted, stereotyped, ritualistic/sameness, self-injurious) and used a data-driven approach to identify functional brain networks associated with the development of each RRB subcategory.
Results:
Higher scores for ritualistic/sameness behavior were associated with less positive fc between visual and control networks at 12 and 24 months. Ritualistic/sameness and stereotyped behaviors were associated with less positive fc between visual and default mode networks at 12 months. At 24 months, stereotyped and restricted behaviors were associated with more positive fc between default mode and control networks. Additionally, at 24 months, stereotyped behavior was associated with more positive fc between dorsal attention and subcortical networks, whereas restricted behavior was associated with more positive fc between default mode and dorsal attention networks. No significant network-level associations were observed for self-injurious behavior.
Conclusions:
These observations mark the earliest known description of functional brain systems underlying RRBs, reinforce the construct validity of RRB subcategories in infants, and implicate specific neural substrates for future interventions targeting RRBs.
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