4.7 Article

Multivariate Searchlight Classification of Structural Magnetic Resonance Imaging in Children and Adolescents with Autism

期刊

BIOLOGICAL PSYCHIATRY
卷 70, 期 9, 页码 833-841

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2011.07.014

关键词

Autism; autism spectrum disorders; biomarker; default mode network; multivariate pattern analysis; support vector machine; voxel-based morphometry

资金

  1. Singer Foundation
  2. Stanford Institute for Neuro-Innovation & Translational Neurosciences
  3. National Institute of Child Health & Human Development [HD047520, HD059205, HD 35469, HD055748]
  4. National Institute of Deafness & Other Communication Disorders [DC0111095]
  5. National Institute of Mental Health [MH084164, K01MH092288, MH64027]
  6. National Science Foundation [BCS/DRL 0750340]
  7. Mosbacher Postdoctoral Fellowship
  8. National Institute of Neurological Disorders and Stroke [NS33355]
  9. Bristol-Myers Squibb
  10. Forest
  11. Pfizer
  12. Astra-Zeneca

向作者/读者索取更多资源

Background: Autism spectrum disorders (ASD) are neurodevelopmental disorders with a prevalence of nearly 1:100. Structural imaging studies point to disruptions in multiple brain areas, yet the precise neuroanatomical nature of these disruptions remains unclear. Characterization of brain structural differences in children with ASD is critical for development of biomarkers that may eventually be used to improve diagnosis and monitor response to treatment. Methods: We use voxel-based morphometry along with a novel multivariate pattern analysis approach and searchlight algorithm to classify structural magnetic resonance imaging data acquired from 24 children and adolescents with autism and 24 age-, gender-, and IQ-matched neurotypical participants. Results: Despite modest voxel-based morphometry differences, multivariate pattern analysis revealed that the groups could be distinguished with accuracies of approximately 90% based on gray matter in the posterior cingulate cortex, medial prefrontal cortex, and bilateral medial temporal lobes-regions within the default mode network. Abnormalities in the posterior cingulate cortex were associated with impaired Autism Diagnostic Interview communication scores. Gray matter in additional prefrontal, lateral temporal, and subcortical structures also discriminated between groups with accuracies between 81% and 90%. White matter in the inferior fronto-occipital and superior longitudinal fasciculi, and the genu and splenium of the corpus callosum, achieved up to 85% classification accuracy. Conclusions: Multiple brain regions, including those belonging to the default mode network, exhibit aberrant structural organization in children with autism. Brain-based biomarkers derived from structural magnetic resonance imaging data may contribute to identification of the neuroanatomical basis of symptom heterogeneity and to the development of targeted early interventions.

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