4.7 Article

Aberrant Striatal Functional Connectivity in Children with Autism

期刊

BIOLOGICAL PSYCHIATRY
卷 69, 期 9, 页码 847-856

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2010.10.029

关键词

Autism; brainstem; development; functional connectivity; insula; striatum

资金

  1. National Alliance for Research on Schizophrenia and Depression
  2. National Institute of Mental Health [K23MH087770]
  3. National Institute of Child Health and Human Development [R01HD065282]
  4. Autism Speaks
  5. Stavros Niarchos Foundation
  6. Alicia Koplowitz Foundation
  7. Leon Levy Foundation

向作者/读者索取更多资源

Background: Models of autism spectrum disorders (ASD) as neural disconnection syndromes have been predominantly supported by examinations of abnormalities in corticocortical networks in adults with autism. Abroader body of research implicates subcortical structures, particularly the striatum, in the physiopathology of autism. Resting state functional magnetic resonance imaging has revealed detailed maps of striatal circuitry in healthy and psychiatric populations and vividly captured maturational changes in striatal circuitry during typical development. Methods: Using resting state functional magnetic resonance imaging, we examined striatal functional connectivity (FC) in 20 children with ASD and 20 typically developing children between the ages of 7.6 and 13.5 years. Whole-brain voxelwise statistical maps quantified within-group striatal FC and between-group differences for three caudate and three putamen seeds for each hemisphere. Results: Children with ASD mostly exhibited prominent patterns of ectopic striatal FC (i.e., functional connectivity present in ASD but not in typically developing children), with increased functional connectivity between nearly all striatal subregions and heteromodal associative and limbic cortex previously implicated in the physiopathology of ASD (e. g., insular and right superior temporal gyrus). Additionally, we found striatal functional hyperconnectivity with the pons, thus expanding the scope of functional alterations implicated in ASD. Secondary analyses revealed ASD-related hyperconnectivity between the pons and insula cortex. Conclusions: Examination of FC of striatal networks in children with ASD revealed abnormalities in circuits involving early developing areas, such as the brainstem and insula, with a pattern of increased FC in ectopic circuits that likely reflects developmental derangement rather than immaturity of functional circuits.

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