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. 2006 Dec 13:6:56.
doi: 10.1186/1471-244X-6-56.

Regional gray matter volumetric changes in autism associated with social and repetitive behavior symptoms

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Regional gray matter volumetric changes in autism associated with social and repetitive behavior symptoms

Donald C Rojas et al. BMC Psychiatry. .

Abstract

Background: Although differences in brain anatomy in autism have been difficult to replicate using manual tracing methods, automated whole brain analyses have begun to find consistent differences in regions of the brain associated with the social cognitive processes that are often impaired in autism. We attempted to replicate these whole brain studies and to correlate regional volume changes with several autism symptom measures.

Methods: We performed MRI scans on 24 individuals diagnosed with DSM-IV autistic disorder and compared those to scans from 23 healthy comparison subjects matched on age. All participants were male. Whole brain, voxel-wise analyses of regional gray matter volume were conducted using voxel-based morphometry (VBM).

Results: Controlling for age and total gray matter volume, the volumes of the medial frontal gyri, left pre-central gyrus, right post-central gyrus, right fusiform gyrus, caudate nuclei and the left hippocampus were larger in the autism group relative to controls. Regions exhibiting smaller volumes in the autism group were observed exclusively in the cerebellum. Significant partial correlations were found between the volumes of the caudate nuclei, multiple frontal and temporal regions, the cerebellum and a measure of repetitive behaviors, controlling for total gray matter volume. Social and communication deficits in autism were also associated with caudate, cerebellar, and precuneus volumes, as well as with frontal and temporal lobe regional volumes.

Conclusion: Gray matter enlargement was observed in areas that have been functionally identified as important in social-cognitive processes, such as the medial frontal gyri, sensorimotor cortex and middle temporal gyrus. Additionally, we have shown that VBM is sensitive to associations between social and repetitive behaviors and regional brain volumes in autism.

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Figures

Figure 1
Figure 1
Correlations between regional gray matter volume and age. Positive (top row) and negative (bottom row) partial correlations, corrected for total gray matter volume, are shown in glass brain projection. SPM(t) map display threshold is FDR < .05. L = left hemisphere. The data in this figure correspond to the linear effects reported in Table 2.
Figure 3
Figure 3
Correlations between regional gray matter volume and ADI-R Repetitive and Stereotyped Behavior Domain in the autism participants. Positive (top row) and negative (bottom row) partial correlations, corrected for total gray matter volume, are shown in glass brain projection. SPM(t) map display threshold is p < .01, uncorrected (Table 4 lists structures surviving small volume correction). L = left hemisphere.
Figure 4
Figure 4
Correlations between regional gray matter volume and ADI-R Social and Communication Domain total scores in the autism participants. Positive (top row) and negative (bottom row) partial correlations, corrected for total gray matter volume, are shown in glass brain projection. SPM(t) map display threshold is p < .01, uncorrected (Table 4 lists structures surviving small volume correction). L = left hemisphere.
Figure 2
Figure 2
Gray matter volume differences between groups, overlaid onto average T1 image from study. Slice numbers (relative to AC-PC origin plane) are shown in upper left corner for each slice. Relative increases (autism > control) are shown in red-orange color scale corresponding to upper right color bar and relative decreases (control > autism) are shown in blue-violet color scale corresponding to lower right color bar. The display threshold is p < .01, uncorrected, but only clusters surviving small volume correction, p < .05, are illustrated (see Table 1 for coordinates and label descriptions).

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References

    1. Bauman M, Kemper TL. Histoanatomic observations of the brain in early infantile autism. Neurology. 1985;35:866–874. - PubMed
    1. Rojas DC, Smith JA, Benkers TL, Camou SL, Reite ML, Rogers SJ. Hippocampus and amygdala volumes in parents of children with autistic disorder. Am J Psychiatry. 2004;161:2038–2044. doi: 10.1176/appi.ajp.161.11.2038. - DOI - PubMed
    1. Schumann CM, Hamstra J, Goodlin-Jones BL, Lotspeich LJ, Kwon H, Buonocore MH, Lammers CR, Reiss AL, Amaral DG. The amygdala is enlarged in children but not adolescents with autism; the hippocampus is enlarged at all ages. J Neurosci. 2004;24:6392–6401. doi: 10.1523/JNEUROSCI.1297-04.2004. - DOI - PMC - PubMed
    1. Haznedar MM, Buchsbaum MS, Wei TC, Hof PR, Cartwright C, Bienstock CA, Hollander E. Limbic circuitry in patients with autism spectrum disorders studied with positron emission tomography and magnetic resonance imaging. American Journal of Psychiatry. 2000;157:1994–2001. doi: 10.1176/appi.ajp.157.12.1994. - DOI - PubMed
    1. Howard MA, Cowell PE, Boucher J, Broks P, Mayes A, Farrant A, Roberts N. Convergent neuroanatomical and behavioural evidence of an amygdala hypothesis of autism. NeuroReport. 2000;11:2931–2935. doi: 10.1097/00001756-200009110-00020. - DOI - PubMed

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