Social visual engagement in infants and toddlers with autism: Early developmental transitions and a model of pathogenesis

被引:122
作者
Kiln, Ami [1 ]
Shultz, Sarah
Jones, Warren
机构
[1] Childrens Healthcare Atlanta, Marcus Autism Ctr, Atlanta, GA 30329 USA
关键词
Autism; Autism spectrum disorders; Social visual engagement; Biological motion; Eye fixation; Infancy; Prodromal; Pathogenesis; Visual imprinting; Epigenetics; LATERAL GENICULATE-NUCLEUS; BIOLOGICAL MOTION PERCEPTION; HIGHER-FUNCTIONING AUTISM; EYE CONTACT; NEURAL MECHANISMS; NEURONAL SYNCHRONIZATION; 6-MONTH-OLD INFANTS; SPECTRUM DISORDERS; FILIAL PREFERENCES; ASPERGER-SYNDROME;
D O I
10.1016/j.neubiorev.2014.10.006
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Efforts to determine and understand the causes of autism are currently hampered by a large disconnect between recent molecular genetics findings that are associated with the condition and the core behavioral symptoms that define the condition. In this perspective piece, we propose a systems biology framework to bridge that gap between genes and symptoms. The framework focuses on basic mechanisms of socialization that are highly-conserved in evolution and are early-emerging in development. By conceiving of these basic mechanisms of socialization as quantitative endophenotypes, we hope to connect genes and behavior in autism through integrative studies of neurodevelopmental, behavioral, and epigenetic changes. These changes both lead to and are led by the accomplishment of specific social adaptive tasks in a typical infant's life. However, based on recent research that indicates that infants later diagnosed with autism fail to accomplish at least some of these tasks, we suggest that a narrow developmental period, spanning critical transitions from reflexive, subcortically-controlled visual behavior to interactional, cortically-controlled and social visual behavior be prioritized for future study. Mapping epigenetic, neural, and behavioral changes that both drive and are driven by these early transitions may shed a bright light on the pathogenesis of autism. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:189 / 203
页数:15
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