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

被引:2
作者
Sanders, Ashley F. P. [1 ,2 ]
Hobbs, Diana A. [1 ,3 ]
Knaus, Tracey A. [1 ]
Beaton, Elliott A. [1 ]
机构
[1] Univ New Orleans, Dept Psychol, 2000 Lakeshore Dr, New Orleans, LA 70148 USA
[2] Washington Univ, Dept Psychiat, Sch Med St Louis, St Louis, MO USA
[3] Washington Univ, Dept Radiol, Sch Med St Louis, St Louis, MO USA
基金
美国国家卫生研究院;
关键词
Brain imaging; DiGeorge syndrome; Emotion processing; Face processing; Genetic deletion; Velocardiofacial syndrome; WHITE-MATTER; FRACTIONAL ANISOTROPY; SOCIAL COGNITION; FACIAL EXPRESSION; NEURAL SYSTEMS; REACTION-TIME; PERCEPTION; CORTEX; MICRODELETION; ABNORMALITIES;
D O I
10.1007/s10803-022-05675-z
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
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.
引用
收藏
页码:4021 / 4034
页数:14
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