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      Alterations of resting state functional connectivity in the default network in adolescents with autism spectrum disorders

      , , , , , ,
      Brain Research
      Elsevier BV

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          Abstract

          Autism spectrum disorders (ASD) are associated with disturbances of neural connectivity. Functional connectivity between neural structures is typically examined within the context of a cognitive task, but also exists in the absence of a task (i.e., "rest"). Connectivity during rest is particularly active in a set of structures called the default network, which includes the posterior cingulate cortex (PCC), retrosplenial cortex, lateral parietal cortex/angular gyrus, medial prefrontal cortex, superior frontal gyrus, temporal lobe, and parahippocampal gyrus. We previously reported that adults with ASD relative to controls show areas of stronger and weaker connectivity within the default network. The objective of the present study was to examine the default network in adolescents with ASD. Sixteen adolescents with ASD and 15 controls participated in a functional MRI study. Functional connectivity was examined between a PCC seed and other areas of the default network. Both groups showed connectivity in the default network. Relative to controls, adolescents with ASD showed widespread weaker connectivity in nine of the eleven areas of the default network. Moreover, an analysis of symptom severity indicated that poorer social skills and increases in restricted and repetitive behaviors and interests correlated with weaker connectivity, whereas poorer verbal and non-verbal communication correlated with stronger connectivity in multiple areas of the default network. These findings indicate that adolescents with ASD show weaker connectivity in the default network than previously reported in adults with ASD. The findings also show that weaker connectivity within the default network is associated with specific impairments in ASD. Copyright 2009 Elsevier B.V. All rights reserved.

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          Author and article information

          Journal
          Brain Research
          Brain Research
          Elsevier BV
          00068993
          February 2010
          February 2010
          : 1313
          : 202-214
          Article
          10.1016/j.brainres.2009.11.057
          2818723
          20004180
          7fd3e3d6-b860-4e11-ae3b-6c47f3708df2
          © 2010

          https://www.elsevier.com/tdm/userlicense/1.0/

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