Abstract

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.

Highlights

  • Autism Spectrum Disorder (ASD) is a neurodevelopmental condition characterized by impairments in (1) social communication and interaction, (2) repetitive and restricted behaviors and interests, and atypical sensory responses (DSM-5, 2013; [1])

  • To move towards bridging the gap between macroscopic and microscopic pathology, we examined the spatial patterns of between-group differences in cortical thickness (CT) for enrichment in (i) genes known to be associated with ASD, and (ii) genes that have previously been linked to repetitive and stereotyped behavior

  • These brain regions were enriched for ASD risk genes, and gene expression modules that are known to be downregulated in the cortex of ASD individuals

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Summary

Introduction

Autism Spectrum Disorder (ASD) is a neurodevelopmental condition characterized by impairments in (1) social communication and interaction, (2) repetitive and restricted behaviors and interests, and atypical sensory responses (DSM-5, 2013; [1]). The clinical phenotype of ASD is highly heterogeneous both within (e.g., across age) and between (e.g., in terms of the severity and profile of core and associated symptoms [2]) individuals. ASD has been linked to hundreds of genetic variants. This suggests that ASD is not a single gene disorder, but has a highly complex (poly)genetic architecture [7]. Combined, these findings highlight inherent difficulties in linking differences in the brain structure to etiological factors, and determining their impact on clinical outcomes in ASD

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