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Probing the Brain in Autism Using fMRI and Diffusion Tensor Imaging
Published on: September 12, 2011
Altered white matter integrity and development in children with autism: a combined voxel-based morphometry and
Paola Mengotti1, Serena D'Agostini, Robert Terlevic
1Ass. La Nostra Famiglia, Pasian di Prato, Udine, Italy. paolo.brambilla@uniud.it
Brain Research Bulletin
|December 15, 2010
Summary
Autism is linked to altered brain development, showing differences in gray and white matter volumes and water diffusion. These neurodevelopmental changes in children with autism may indicate early cerebral dysconnectivity.
Area of Science:
- Neuroscience
- Developmental Psychology
- Radiology
Background:
- Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition.
- Investigating brain structure and function in autism is crucial for understanding its underlying mechanisms.
Purpose of the Study:
- To explore neurodevelopmental differences in gray and white matter in children with autism.
- To utilize voxel-based morphometry (VBM) and diffusion-weighted imaging (DWI) for a combined analysis.
Main Methods:
- Magnetic resonance imaging (MRI) was performed on children with autism and typically developing controls.
- Voxel-based morphometry (VBM) with a customized template and diffusion-weighted imaging (DWI) for apparent diffusion coefficients (ADC) were used.
- Regions of interest (ROIs) were analyzed for volumetric and diffusion properties.
Main Results:
- Individuals with autism showed increased white matter volumes in specific brain regions (e.g., right inferior frontal gyrus, hippocampus).
- Gray matter volume alterations were observed in autism, with increases in some areas (e.g., inferior temporal gyri) and decreases in others (e.g., right inferior frontal gyrus).
- Abnormally increased ADC values in frontal cortex and corpus callosum, along with age-related diffusion changes, were noted in autism.
Conclusions:
- Findings suggest early-phase cerebral dysconnectivity in autism.
- Altered white matter maturation trajectories in frontal and parietal lobes may be a neurodevelopmental marker for autism.
- These brain differences could contribute to the cognitive and social deficits observed in autism.

