Literature DB >> 28042973

Disordered cortical connectivity underlies the executive function deficits in children with autism spectrum disorders.

Yvonne M Y Han1, Agnes S Chan2.   

Abstract

The present study examined the executive function and cortical connectivity of children with autism spectrum disorders (ASD) and investigated whether the executive function deficits exhibited by these children were differentially affected and associated with the cortical connectivity. The present study compared high-functioning (HFA) and low-functioning (LFA) children with typically developing children (TDC) on their executive functions as measured by the Hong Kong List Learning Test, D2 Test of Concentration, Five Point Test, Children's Color Trail Test, Tower of California Test, and Go/No-Go task and neural connectivity as measured by theta coherence in the distributed fronto-parietal network. Thirty-eight children with ASD (19 HFA and 19 LFA) and 28 TDC children, aged 8-17 years, participated voluntarily in the study. The results on executive function showed that the LFA group demonstrated the poorest performance as exhibited by their Executive Composite and individual executive function scores, while the TDC group exhibited the highest. These results have extended the findings of previous studies in demonstrating that HFA and LFA children have significant differences in their degree of executive function deficits. The results on neural connectivity also showed that children with ASD demonstrated a different pattern of electroencephalography (EEG) coherence from TDC children, as demonstrated by the significantly elevated theta coherence in the fronto-parietal network, and that the severity of executive dysfunction between high- and low-functioning children with ASD was found to be associated with the disordered neural connectivity in these children.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Autism; Children; EEG coherence; Executive dysfunction; Theta

Mesh:

Year:  2016        PMID: 28042973     DOI: 10.1016/j.ridd.2016.12.010

Source DB:  PubMed          Journal:  Res Dev Disabil        ISSN: 0891-4222


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