4.6 Article

Longitudinal Changes in Cortical Thickness in Adolescents with Autism Spectrum Disorder and Their Association with Restricted and Repetitive Behaviors

Journal

GENES
Volume 12, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/genes12122024

Keywords

autism spectrum disorder; cortical thickness; restricted and repetitive behaviors; genetics

Funding

  1. German Research Foundation (DFG) under the Heisenberg Programme [EC480/1-1, EC480/2-1]

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This study revealed significantly reduced cortical thinning in several brain regions related to autism symptoms in individuals with ASD, with these neuroanatomical differences enriched for genes associated with ASD at a genetic and transcriptomic level. Furthermore, intra-individual differences in cortical thickness correlated with the severity of repetitive behaviors within individuals with ASD.
The neuroanatomy of autism spectrum disorder (ASD) shows highly heterogeneous developmental trajectories across individuals. Mapping atypical brain development onto clinical phenotypes, and establishing their molecular underpinnings, is therefore crucial for patient stratification and subtyping. In this longitudinal study we examined intra- and inter-individual differences in the developmental trajectory of cortical thickness (CT) in childhood and adolescence, and their genomic underpinnings, in 33 individuals with ASD and 37 typically developing controls (aged 11-18 years). Moreover, we aimed to link regional atypical CT development to intra-individual variations in restricted and repetitive behavior (RRB) over a two-year time period. Individuals with ASD showed significantly reduced cortical thinning in several of the brain regions functionally related to wider autism symptoms and traits (e.g., fronto-temporal and cingulate cortices). The spatial patterns of the neuroanatomical differences in CT were enriched for genes known to be associated with ASD at a genetic and transcriptomic level. Further, intra-individual differences in CT correlated with within-subject variability in the severity of RRBs. Our findings represent an important step towards characterizing the neuroanatomical underpinnings of ASD across development based upon measures of CT. Moreover, our findings provide important novel insights into the link between microscopic and macroscopic pathology in ASD, as well as their relationship with different clinical ASD phenotypes.

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