| Literature DB >> 35034115 |
Ya Wang1,2, Dan Hu2, Zhengwang Wu2, Li Wang2, Wenhua Huang1, Gang Li2.
Abstract
Converging evidence supports that a collection of brain regions is functionally or anatomically abnormal in autistic subjects. Structural covariance networks (SCNs) representing patterns of coordinated regional maturation are widely used to study abnormalities associated with neurodisorders. However, the possible developmental changes of SCNs in autistic individuals during the first 2 postnatal years, which features dynamic development and can potentially serve as biomarkers, remain unexplored. To fill this gap, for the first time, SCNs of cortical thickness and surface area were constructed and investigated in infants at high familial risk for autism and typically developing infants in this study. Group differences of SCNs emerge at 12 months of age in surface area. By 24 months of age, the autism group shows significantly increased integration, decreased segregation, and decreased small-worldness, compared with controls. The SCNs of surface area are deteriorated and shifted toward randomness in autistic infants. The abnormal brain regions changed during development, and the group differences of the left lateral occipital cortex become more prominent with age. These results indicate that autism has more significant influences on coordinated development of surface area than that of cortical thickness and the occipital cortex maybe an important biomarker of autism during infancy.Entities:
Keywords: autism spectrum disorder; cortical thickness; infants; structural covariance network; surface area
Mesh:
Year: 2022 PMID: 35034115 PMCID: PMC9433424 DOI: 10.1093/cercor/bhab448
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 4.861