Abstract

Autism spectrum disorder (ASD) is associated with disruption of local- and long-range functional connectivity (FC). The direction of those changes in FC (increase or decrease), however, is inconsistent across studies. Further, age-dependent changes of distance-specific FC in ASD remain unclear. In this study, we used resting-state functional magnetic resonance imaging data from sixty-four typical controls (TC) and sixty-four patients with ASD, whom we further classified into child (<11 years), adolescent (11–18 years) and adult cohorts (>18 years). Functional connectivity (FC) analysis was conducted at voxel level. We employed a three-way analysis of covariance on FC to conduct statistical analyses. Results revealed that patients with ASD had lower FC than TC in cerebellum, fusiform gyrus, inferior occipital gyrus and posterior inferior temporal gyrus. Significant diagnosis-by-distance interaction was observed in ASD patients with reduced short-range and long-range FC in posterior cingulate cortex and medial prefrontal cortex. Importantly, we found significant diagnosis-by-age-by-distance interaction in orbitofrontal cortex with short-range FC being lower in autistic children, but –to a less extent– higher in autistic adults. Our findings suggest a major role of connection length in development changes of FC in ASD. We hope our study will facilitate deeper understanding of the neural mechanisms underlying ASD.

Highlights

  • IntroductionDevelopment studies in the healthy brain revealed that short- and long-range functional connectivity (FC) differentially changes as a function of age

  • We investigated the influence of anatomical distance and age on functional connectivity (FC) changes in Autism spectrum disorder (ASD)

  • We found lowered FC in cerebellum, fusiform gyrus and occipital cortex in ASD

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Summary

Introduction

Development studies in the healthy brain revealed that short- and long-range FC differentially changes as a function of age. It was demonstrated that long-range and short-range FC increases and decreases with age, respectively[14,15,16] This developmental profile of FC in the human brain is thought to contribute to efficient information integration for higher cognition, as well as to segregation for specialized information processing. To the best of our knowledge, there are only a few studies that investigated shortand long-range FC development in ASD. These revealed that short-range hyper-connectivity and long-range under-connectivity in autism may concurrently emerge due to problems with synapse pruning or formation[17,18]. We hypothesized that patients with ASD showed abnormal development of FC for specific anatomical distances

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