4.7 Article

Mapping Brain Abnormalities in Boys with Autism

期刊

HUMAN BRAIN MAPPING
卷 30, 期 12, 页码 3887-3900

出版社

WILEY
DOI: 10.1002/hbm.20814

关键词

autism; TBM; white matter; gray matter; cerebellum; morphometry

资金

  1. National Center for Research Resources [AG016570, EB01651, RR019771]
  2. NIDA [MH/DA52176, RR13642, MH655166]
  3. National Institute of Aging
  4. National Institute for Biomedical Imaging and Bioengineering, Child and Parent Resource Institute
  5. London Health Science Foundation
  6. Ontario Mental Health Foundation
  7. Hospital for Sick Children Foundation
  8. NIMH

向作者/读者索取更多资源

Children with autism spectrum disorder (ASD) exhibit characteristic cognitive and behavioral differences, but no systematic pattern of neuroanatomical differences has been consistently found. Recent neurodevelopmental models posit an abnormal early surge in subcortical white matter growth in at least some autistic children, perhaps normalizing by adulthood, but other studies report subcortical white matter deficits. To investigate the profile of these alterations in 3D, we mapped brain volumetric differences using a relatively new method, tensor-based morphometry. 3D T1-weighted brain MRIs of 24 mate children with ASD (age: 9.5 years +/- 3.2 SD) and 26 age-matched healthy controls (age: 10.3 +/- 2.4 SD) were fluidly registered to match a common anatomical template. Autistic children had significantly enlarged frontal lobes (by 3.6% on the left and 5.1% on the right), and all other lobes of the brain were enlarged significantly, or at trend level. By analyzing the applied deformations statistically point-by-point, we detected significant gray matter volume deficits in bilateral parietal, left temporal and left occipital lobes (P = 0.038, corrected), trend-level cerebral white matter volume excesses, and volume deficits in the cerebellar vermis, adjacent to volume excesses in other cerebellar regions. This profile of excesses and deficits in adjacent regions may (1) indicate impaired neuronal connectivity, resulting from aberrant myelination and/or an inflammatory process, and (2) help to understand inconsistent findings of regional brain tissue excesses and deficits in autism. Hum Brain Mapp 30:3887-3900, 2009. (C) 2009 Wiley-Liss, Inc.

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