Biological Psychiatry Global Open Science (Jan 2023)

A Prospective Evaluation of Infant Cerebellar-Cerebral Functional Connectivity in Relation to Behavioral Development in Autism Spectrum Disorder

  • Zoë W. Hawks,
  • Alexandre Todorov,
  • Natasha Marrus,
  • Tomoyuki Nishino,
  • Muhamed Talovic,
  • Mary Beth Nebel,
  • Jessica B. Girault,
  • Savannah Davis,
  • Scott Marek,
  • Benjamin A. Seitzman,
  • Adam T. Eggebrecht,
  • Jed Elison,
  • Stephen Dager,
  • Matthew W. Mosconi,
  • Lawrence Tychsen,
  • Abraham Z. Snyder,
  • Kelly Botteron,
  • Annette Estes,
  • Alan Evans,
  • Guido Gerig,
  • Heather C. Hazlett,
  • Robert C. McKinstry,
  • Juhi Pandey,
  • Robert T. Schultz,
  • Martin Styner,
  • Jason J. Wolff,
  • Lonnie Zwaigenbaum,
  • Lori Markson,
  • Steven E. Petersen,
  • John N. Constantino,
  • Desirée A. White,
  • Joseph Piven,
  • John R. Pruett, Jr.

Journal volume & issue
Vol. 3, no. 1
pp. 149 – 161

Abstract

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Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder diagnosed based on social impairment, restricted interests, and repetitive behaviors. Contemporary theories posit that cerebellar pathology contributes causally to ASD by disrupting error-based learning (EBL) during infancy. The present study represents the first test of this theory in a prospective infant sample, with potential implications for ASD detection. Methods: Data from the Infant Brain Imaging Study (n = 94, 68 male) were used to examine 6-month cerebellar functional connectivity magnetic resonance imaging in relation to later (12/24-month) ASD-associated behaviors and outcomes. Hypothesis-driven univariate analyses and machine learning–based predictive tests examined cerebellar–frontoparietal network (FPN; subserves error signaling in support of EBL) and cerebellar–default mode network (DMN; broadly implicated in ASD) connections. Cerebellar-FPN functional connectivity was used as a proxy for EBL, and cerebellar-DMN functional connectivity provided a comparative foil. Data-driven functional connectivity magnetic resonance imaging enrichment examined brain-wide behavioral associations, with post hoc tests of cerebellar connections. Results: Cerebellar-FPN and cerebellar-DMN connections did not demonstrate associations with ASD. Functional connectivity magnetic resonance imaging enrichment identified 6-month correlates of later ASD-associated behaviors in networks of a priori interest (FPN, DMN), as well as in cingulo-opercular (also implicated in error signaling) and medial visual networks. Post hoc tests did not suggest a role for cerebellar connections. Conclusions: We failed to identify cerebellar functional connectivity–based contributions to ASD. However, we observed prospective correlates of ASD-associated behaviors in networks that support EBL. Future studies may replicate and extend network-level positive results, and tests of the cerebellum may investigate brain-behavior associations at different developmental stages and/or using different neuroimaging modalities.

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