amygdala engagement in response to subthreshold presentations of anxious face stimuli in adults with autism spectrum disorders preliminary insights杏仁核参与反应阈下演讲焦虑的脸刺激在成人自闭症谱系障碍的初步见解.pdfVIP
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amygdala engagement in response to subthreshold presentations of anxious face stimuli in adults with autism spectrum disorders preliminary insights杏仁核参与反应阈下演讲焦虑的脸刺激在成人自闭症谱系障碍的初步见解
Amygdala Engagement in Response to Subthreshold
Presentations of Anxious Face Stimuli in Adults with
Autism Spectrum Disorders: Preliminary Insights
1,2,3 1 1 1 1,3
Geoffrey B. C. Hall *, Krissy A. R. Doyle , Jeremy Goldberg , Dianne West , Peter Szatmari
1 Department of Psychiatry and Behavioural Neurosciences, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada, 2 The Brain-Body Institute, St.
Joseph’s Healthcare, Hamilton, Ontario, Canada, 3 Offord Centre for Child Studies, McMaster University, Hamilton, Ontario, Canada
Abstract
Current theoretical models of autism spectrum disorders (ASD) have proposed that impairments in the processing of social/
emotional information may be linked to amygdala dysfunction. However, the extent to which amygdala functions are
compromised in ASD has become a topic of debate in recent years. In a jittered functional magnetic resonance imaging
study, sub-threshold presentations of anxious faces permitted an examination of amygdala recruitment in 12 high
functioning adult males with ASD and 12 matched controls. We found heightened neural activation of the amygdala in both
high functioning adults with ASD and matched controls. Neither the intensity nor the time-course of amygdala activation
differed between the groups. However, the adults with ASD showed significantly lower levels of fusiform activation during
the trials compared to controls. Our findings suggest that in ASD, the transmission of socially salient information along sub-
cortical pathways is intact: and yet the signaling of this information to structures downstream may be impoverished, and
the pathways that facilitate subsequent processing deficient.
Citation: Hall GBC,
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