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Meta-analysis of Voxel-Based Neuroimaging Studies using Seed-based d Mapping with Permutation of Subject Images (SDM-PSI)
Published on: November 27, 2019
Smaller insula and inferior frontal volumes in young adults with pervasive developmental disorders
Hirotaka Kosaka1, Masao Omori, Toshio Munesue
1Department of Neuropsychiatry, Faculty of Medical Sciences, University of Fukui, Eiheiji, Fukui, 910-1193, Japan. hirotaka@u-fukui.ac.jp
Insights
Young adults with high-functioning pervasive developmental disorders (PDD) show reduced gray matter volume in specific brain regions. These findings suggest brain structure differences in PDD may not be linked to intelligence quotient (IQ).
Area of Science:
- Neuroimaging
- Developmental Neuroscience
- Psychiatry
Background:
- Infants with pervasive developmental disorders (PDD) exhibit enlarged head circumference and brain weight.
- Volumetric studies indicate enlarged brain volumes in children with PDD.
- Little is known about brain volume abnormalities in young adults with PDD.
Purpose of the Study:
- To investigate gray matter (GM) volume differences in young adults with high-functioning PDD.
- To explore the relationship between GM volume, Autism Spectrum Quotient (ASQ) scores, and Full Scale Intelligence Quotient (FSIQ) in this population.
Main Methods:
- T1-weighted volumetric magnetic resonance imaging (MRI) was used.
- 32 males with high-functioning PDD and 40 age-matched male controls participated.
- Voxel-based morphometry (VBM) with Diffeomorphic Anatomical Registration using Exponentiated Lie algebra (DARTEL) was employed for regional GM volume comparison.
Main Results:
- The high-functioning PDD group exhibited significantly less GM volume in the right insula, right inferior frontal gyrus, and right inferior parietal lobule compared to controls.
- Smaller GM volumes were confirmed in the right insula and inferior frontal gyrus.
- Negative correlations were observed between ASQ scores and GM volume in these regions, but no significant correlation was found with FSIQ.
Conclusions:
- Reduced GM volumes in specific brain regions (insula, inferior frontal gyrus) are present in young adults with high-functioning PDD.
- These structural differences may underlie the clinical features of PDD, independent of FSIQ.
- The insular cortex's role as a neurocognitive relay area may be crucial in understanding PDD's complex manifestations.
Abstract:
Enlarged head circumference and increased brain weight have been reported in infants with pervasive developmental disorders (PDD), and volumetric studies suggest that children with PDD have abnormally enlarged brain volumes. However, little is known about brain volume abnormalities in young adults with PDD. We explored gray matter (GM) volume in young adults with PDD. T1-weighted volumetric images were acquired with a 3-T magnetic resonance scanner from 32 males with high-functioning PDD (23.8+/-4.2 years; Full Scale Intelligence Quotient [FSIQ]=101.6+/-15.6) and 40 age-matched normal male control subjects (22.5+/-4.3 years; FSIQ=109.7+/-7.9). Regional GM volumes were compared between the two groups using voxel-based morphometry (VBM) with the Diffeomorphic Anatomical Registration using Exponentiated Lie algebra (DARTEL). Compared with the control group, the high-functioning PDD group showed significantly less GM in the right insula, the right inferior frontal gyrus, and the right inferior parietal lobule. A conservative threshold confirmed considerably smaller volumes in the right insula and inferior frontal gyrus. In these areas, negative correlations were found between Autism Spectrum Quotient scores and GM volume, although no significant correlations were found between each subject's FSIQ and GM volume. No regions showed greater GM volumes in the high-functioning PDD group. The insular cortex, which works as a relay area for multiple neurocognitive systems, may be one of the key regions underlying the complex clinical features of PDD. These smaller GM volumes in high-functioning PDD subjects may reflect the clinical features of PDD itself, rather than FSIQ.
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