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Updated: Mar 8, 2026

Testing Sensory and Multisensory Function in Children with Autism Spectrum Disorder
Published on: April 22, 2015
Network over-connectivity differentiates autism spectrum disorder from other developmental disorders in toddlers: A
E Conti1, J Mitra2, S Calderoni1
1Department of Developmental Neuroscience, Stella Maris Scientific Institute, Pisa, Italy.
Insights
This study found over-connectivity in the brains of toddlers with Autism Spectrum Disorder (ASD) compared to other developmental disorders. These brain connectivity differences emerge early, aiding in differential diagnosis.
Area of Science:
- Neuroscience
- Developmental Neuroscience
- Pediatric Neurology
Background:
- Autism Spectrum Disorder (ASD) diagnosis in toddlers is challenging.
- Existing brain connectivity studies in ASD often lack specificity by not comparing with other developmental disorders (other-DD).
- Early identification of specific neurobiological markers is crucial for timely intervention.
Purpose of the Study:
- To investigate distinct brain connectivity patterns in toddlers with ASD versus other-DD.
- To identify early neuroimaging markers differentiating ASD from other neurodevelopmental conditions.
- To advance understanding of the neural underpinnings of ASD in early childhood.
Main Methods:
- Recruited toddlers (<36 months) diagnosed with ASD (n=32) or other-DD (n=16) per DSM-IV TR.
- Acquired structural and diffusion MRI data for whole-brain tractography.
- Utilized Network Based Statistics (NBS) on connectivity matrices (DNUM, DFA) to compare ASD and other-DD groups.
Main Results:
- Toddlers with ASD exhibited a significant pattern of over-connectivity (higher DNUM and DFA) compared to the other-DD group (P < 0.05).
- This over-connectivity was prominent in fronto-temporal networks and basal ganglia.
- No significant differences were found when comparing other-DD to ASD.
Conclusions:
- This study provides the first network-based diffusion MRI evidence differentiating brain connectivity in toddlers with ASD from those with other-DD.
- Distinct connectivity patterns, specifically over-connectivity in ASD, are detectable in early development.
- Findings suggest potential neuroimaging biomarkers for early ASD diagnosis when clinical presentation is ambiguous.
Abstract:
Advanced connectivity studies in toddlers with Autism Spectrum Disorder (ASD) are increasing and consistently reporting a disruption of brain connectivity. However, most of these studies compare ASD and typically developing subjects, thus providing little information on the specificity of the abnormalities detected in comparison with other developmental disorders (other-DD). We recruited subjects aged below 36 months who received a clinical diagnosis of Neurodevelopmental Disorder (32 ASD and 16 other-DD including intellectual disability and language disorder) according to DSM-IV TR. Structural and diffusion MRI were acquired to perform whole brain probabilistic and anatomically constrained tractography. Network connectivity matrices were built encoding the number of streamlines (DNUM ) and the tract-averaged fractional anisotropy (DFA ) values connecting each pair of cortical and subcortical regions. Network Based Statistics (NBS) was finally applied on the connectivity matrices to evaluate the network differences between the ASD and other-DD groups. The network differences resulted in an over-connectivity pattern (i.e., higher DNUM and DFA values) in the ASD group with a significance of P < 0.05. No contra-comparison results were found. The over-connectivity pattern in ASD occurred in networks primarily involving the fronto-temporal nodes, known to be crucial for social-skill development and basal ganglia, related to restricted and repetitive behaviours in ASD. To our knowledge, this is the first network-based diffusion study comparing toddlers with ASD and those with other-DD. Results indicate the detection of different connectivity patterns in ASD and other-DD at an age when clinical differential diagnosis is often challenging. Hum Brain Mapp 38:2333-2344, 2017. © 2017 Wiley Periodicals, Inc.
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