4.7 Article

The Development of the Neural Substrates of Cognitive Control in Adolescents with Autism Spectrum Disorders

期刊

BIOLOGICAL PSYCHIATRY
卷 76, 期 5, 页码 412-421

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2013.08.036

关键词

Adolescence; autism spectrum disorders; cognitive control; development; fMRI; response inhibition

资金

  1. National Institute of Mental Health [1-K-08 MH074967-01, 2R01 MH059883-05A1, 1R24MH081807, K23MH087708, R01MH084895, K-08]
  2. Building Interdisciplinary Research Careers in Women's Health Award - National Institute of Child Health and Human Development, Office of Research on Women's Health, Office of Dietary Supplements [K12 HD051958]
  3. National Institute of Aging
  4. National Alliance for Research on Schizophrenia and Depression (Atherton Foundation)
  5. GlaxoSmithKline

向作者/读者索取更多资源

Background: Autism spectrum disorders (ASDs) involve impairments in cognitive control. In typical development (TYP), neural systems underlying cognitive control undergo substantial maturation during adolescence. Development is delayed in adolescents with ASD. Little is known about the neural substrates of this delay. Methods: We used event-related functional magnetic resonance imaging and a cognitive control task involving overcoming a prepotent response tendency to examine the development of cognitive control in young (ages 12-15; n = 13 with ASD and n = 13 with TYP) and older (ages 16-18; n = 14 with ASD and n = 14 with TYP) adolescents with whole-brain voxelwise univariate and task-related functional connectivity analyses. Results: Older ASD and TYP showed reduced activation in sensory and premotor areas relative to younger ones. The older ASD group showed reduced left parietal activation relative to TYP. Functional connectivity analyses showed a significant age by group interaction with the older ASD group exhibiting increased functional connectivity strength between the ventrolateral prefrontal cortex and the anterior cingulate cortex, bilaterally. This functional connectivity strength was related to task performance in ASD, whereas that between dorsolateral prefrontal cortex and parietal cortex (Brodmann areas 9 and 40) was related to task performance in TYP. Conclusions: Adolescents with ASD rely more on reactive cognitive control, involving last-minute conflict detection and control implementation by the anterior cingulate cortex and ventrolateral prefrontal cortex, versus proactive cognitive control requiring processing by dorsolateral prefrontal cortex and parietal cortex. Findings await replication in larger longitudinal studies that examine their functional consequences and amenability to intervention.

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