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Gaze-fixation, brain activation, and amygdala volume in unaffected siblings of individuals with autism
被引:179
作者:
Dalton, Kim M.
Nacewicz, Brendon M.
Alexander, Andrew L.
Davidson, Richard J.
机构:
[1] Univ Wisconsin, Waisman Ctr, Madison, WI 53705 USA
[2] Univ Wisconsin, Waisman Lab Funct Brain Imaging & Behav, Madison, WI 53705 USA
[3] Univ Wisconsin, Dept Psychol, Madison, WI 53705 USA
[4] Univ Wisconsin, Dept Psychiat, Madison, WI 53705 USA
[5] Univ Wisconsin, Dept Med Phys, Madison, WI 53705 USA
关键词:
amygdala;
autism;
child/adolescent psychiatry;
cognitive neuroscience;
functional imaging;
structural imaging;
D O I:
10.1016/j.biopsych.2006.05.019
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Background: The broad autism phenotype includes subclinical autistic characteristics found to have a higher prevalence in unaffected family members of individuals with autism, These characteristics primarily affect the social aspects of language, communication, and human interaction. The current research focuses on possible neurobehavioral characteristics associated with the broad autism phenotype. Methods: We used a,face-processing task associated with atypical patterns of gaze fixation and brain function in autism while collecting brain functional magnetic resonance imaging (fMRI) and eye tracking in unaffected siblings of individuals with autism. Results. We found robust differences in gaze fixation and brain function in response to images of human faces in unaffected siblings compared with typically developing control individuals. 7 he siblings' gaze fixations and brain activation patterns during the face processing task were similar to that of the autism group and showed decreased gaze fixation along with diminished fusiform activation compared with the control group. Furthermore, amygdala volume in the siblings was similar to the autism group and was significantly reduced compared with the control group. Conclusions: Together, these findings provide compelling evidence for differences in social/emotional processing and underlying neural circuitry in siblings of individuals with autism, supporting the notion of unique endophenotypes associated with the broad autism phenotype.
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页码:512 / 520
页数:9
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