Structural Connectivity and Emotion Recognition Impairment in Children and Adolescents with Chromosome 22q11.2 Deletion Syndrome

被引:0
|
作者
Ashley F. P. Sanders
Diana A. Hobbs
Tracey A. Knaus
Elliott A. Beaton
机构
[1] University of New Orleans,Department of Psychology
[2] Washington University School of Medicine in St. Louis,Department of Psychiatry
[3] Washington University School of Medicine in St. Louis,Department of Radiology
来源
Journal of Autism and Developmental Disorders | 2023年 / 53卷
关键词
Brain imaging; DiGeorge syndrome; Emotion processing; Face processing; Genetic deletion; Velocardiofacial syndrome;
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摘要
Children with chromosome 22q11.2 deletion syndrome (22q11.2DS) exhibit impaired ability to process and understand emotions in others. We measured structural connectivity in children and adolescents with 22q11.2DS (n = 28) and healthy controls (n = 29). Compared to controls, those with 22q11.2DS had poorer social skills and more difficulty recognizing facial emotions. Children with 22q11.2DS also had higher fractional anisotropic diffusion in right amygdala to fusiform gyrus white matter pathways. Right amygdala to fusiform gyrus fractional anisotropy values partially mediated the relationship between 22q11.2DS and social skills, as well as the relationship between 22q11.2DS and emotion recognition accuracy. These findings provide insight into the neural origins of social skills deficits seen in 22q11.2DS and may serve as a biomarker for risk of future psychiatric problems.
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页码:4021 / 4034
页数:13
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