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

Neuroimage
|February 4, 2010
PubMed

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.