Social endophenotypes in autism spectrum disorder: A scoping review

被引:9
|
作者
Tiede, Gabrielle M. [1 ]
Walton, Katherine M. [1 ]
机构
[1] Ohio State Univ, 241 McCampbell Hall,1581 Dodd Dr, Columbus, OH 43210 USA
关键词
autism; early detection; endophenotypes; LOW GENETIC RISK; INFANT SIBLINGS; ASPERGER-SYNDROME; YOUNGER SIBLINGS; DEVELOPMENTAL PSYCHOPATHOLOGY; UNAFFECTED SIBLINGS; FACE RECOGNITION; 6-MONTH-OLD INFANTS; EXECUTIVE FUNCTION; AMYGDALA VOLUME;
D O I
10.1017/S0954579420000577
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Endophenotypes are measurable markers of genetic vulnerability to current or future disorder. Autism spectrum disorder (ASD) is well-suited to be examined within an endophenotype framework given past and current emphases on the broader autism phenotype and early detection. We conducted a scoping review to identify potential socially-related endophenotypes of ASD. We focused on paradigms related to sociality (e.g., theory of mind (TOM), social attention), which comprise most of this literature. We integrated findings from traditional behavioral paradigms with brain-based measures (e.g., electroencephalography, functional magnetic resonance imaging). Broadly, infant research regarding social attention and responsivity (Research Domain Criteria (RDoC) domain of affiliation) and attention to faces and voices (social communication) finds consistent abnormality in vulnerable infant siblings. Several additional paradigms that have shown differences in vulnerable infants and young children include animacy perception tasks (perception and understanding of others), measures of recognition and response to familiar faces (attachment), and joint attention and false-belief tasks (understanding mental states). Research areas such as alexithymia (the perception and understanding of self), empathic responding, and vocal prosody may hold interest; however, challenges in measurement across populations and age ranges is a limiting factor. Future work should address sex differences and age dependencies, specificity to ASD, and heterogeneous genetic pathways to disorder within samples individuals with ASD and relatives.
引用
收藏
页码:1381 / 1409
页数:29
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