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

Autism Cerebellum Development Error-based learning Functional connectivity Infancy

Journal

Biological psychiatry global open science
ISSN: 2667-1743
Titre abrégé: Biol Psychiatry Glob Open Sci
Pays: United States
ID NLM: 9918227369306676

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 17 06 2021
revised: 03 12 2021
accepted: 04 12 2021
entrez: 30 1 2023
pubmed: 16 12 2021
medline: 16 12 2021
Statut: epublish

Résumé

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. Data from the Infant Brain Imaging Study ( 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. 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.

Sections du résumé

Background UNASSIGNED
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 UNASSIGNED
Data from the Infant Brain Imaging Study (
Results UNASSIGNED
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 UNASSIGNED
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.

Identifiants

pubmed: 36712571
doi: 10.1016/j.bpsgos.2021.12.004
pii: S2667-1743(21)00161-0
pmc: PMC9874081
doi:

Types de publication

Journal Article

Langues

eng

Pagination

149-161

Subventions

Organisme : NICHD NIH HHS
ID : P50 HD103525
Pays : United States
Organisme : NICHD NIH HHS
ID : P50 HD103573
Pays : United States

Informations de copyright

© 2021 The Authors.

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Auteurs

Zoë W Hawks (ZW)

Department of Psychological and Brain Sciences, Washington University in St. Louis, St. Louis, Missouri.

Alexandre Todorov (A)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Natasha Marrus (N)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Tomoyuki Nishino (T)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Muhamed Talovic (M)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Mary Beth Nebel (MB)

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Jessica B Girault (JB)

Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Savannah Davis (S)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Scott Marek (S)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Benjamin A Seitzman (BA)

Department of Neurology, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Adam T Eggebrecht (AT)

Mallinckrodt Institute of Radiology, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Jed Elison (J)

Institute of Child Development, University of Minnesota, Minneapolis, Minnesota.

Stephen Dager (S)

Departments of Radiology, University of Washington, Seattle, Washington.

Matthew W Mosconi (MW)

Life Span Institute and Clinical Child Psychology Program, University of Kansas, Lawrence, Kansas.

Lawrence Tychsen (L)

Department of Ophthalmology and Visual Sciences, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Abraham Z Snyder (AZ)

Department of Neurology, Washington University School of Medicine in St. Louis, St. Louis, Missouri.
Mallinckrodt Institute of Radiology, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Kelly Botteron (K)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Annette Estes (A)

Speech and Hearing Sciences, University of Washington, Seattle, Washington.

Alan Evans (A)

McConnell Brain Imaging Center, Montreal Neurological Institute, Montreal, Quebec, Canada.

Guido Gerig (G)

Department of Computer Science and Engineering, Tandon School of Engineering, New York University, New York, New York.

Heather C Hazlett (HC)

Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Robert C McKinstry (RC)

Mallinckrodt Institute of Radiology, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Juhi Pandey (J)

Center for Autism Research, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania.

Robert T Schultz (RT)

Center for Autism Research, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania.

Martin Styner (M)

Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Jason J Wolff (JJ)

Department of Educational Psychology, University of Minnesota, Minneapolis, Minnesota.

Lonnie Zwaigenbaum (L)

Department of Psychiatry, University of Alberta, Edmonton, Alberta, Canada.

Lori Markson (L)

Department of Psychological and Brain Sciences, Washington University in St. Louis, St. Louis, Missouri.

Steven E Petersen (SE)

Department of Neurology, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

John N Constantino (JN)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Desirée A White (DA)

Department of Psychological and Brain Sciences, Washington University in St. Louis, St. Louis, Missouri.

Joseph Piven (J)

Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

John R Pruett (JR)

Department of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, Missouri.

Classifications MeSH