Social reward network connectivity differs between autistic and neurotypical youth during social interaction.

Adolescence Autism spectrum disorders Functional MRI (fMRI) Social neuroscience

Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
07 Jun 2023
Historique:
pubmed: 19 6 2023
medline: 19 6 2023
entrez: 19 6 2023
Statut: epublish

Résumé

A core feature of autism is difficulties with social interaction. Atypical social motivation is proposed to underlie these difficulties. However, prior work testing this hypothesis has shown mixed support and has been limited in its ability to understand real-world social-interactive processes in autism. We attempted to address these limitations by scanning neurotypical and autistic youth (n = 86) during a text-based reciprocal social interaction that mimics a "live" chat and elicits social reward processes. We focused on task-evoked functional connectivity (FC) of regions responsible for motivational-reward and mentalizing processes within the broader social reward circuitry. We found that task-evoked FC between these regions was significantly modulated by social interaction and receipt of social-interactive reward. Compared to neurotypical peers, autistic youth showed significantly greater task-evoked connectivity of core regions in the mentalizing network (e.g., posterior superior temporal sulcus) and the amygdala, a key node in the reward network. Furthermore, across groups, the connectivity strength between these mentalizing and reward regions was negatively correlated with self-reported social motivation and social reward during the scanner task. Our results highlight an important role of FC within the broader social reward circuitry for social-interactive reward. Specifically, greater context-dependent FC (i.e., differences between social engagement and non-social engagement) may indicate an increased "neural effort" during social reward and relate to differences in social motivation within autistic and neurotypical populations.

Identifiants

pubmed: 37333161
doi: 10.1101/2023.06.05.543807
pmc: PMC10274709
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH107441
Pays : United States

Auteurs

Hua Xie (H)

Neuroscience and Cognitive Science Program, University of Maryland, College Park, Maryland, USA.
Department of Psychology, University of Maryland, College Park, Maryland, USA.
Center for Neuroscience Research, Children's National Hospital, Washington, D.C., USA.
The George Washington University School of Medicine, Washington, D.C., USA.

Dustin Moraczewski (D)

Data Science and Sharing Team, National Institute of Mental Health, Bethesda, Maryland, USA.

Kathryn A McNaughton (KA)

Neuroscience and Cognitive Science Program, University of Maryland, College Park, Maryland, USA.
Department of Psychology, University of Maryland, College Park, Maryland, USA.

Katherine R Warnell (KR)

Department of Psychology, Texas State University, San Marcos, Texas, USA.

Diana Alkire (D)

Neuroscience and Cognitive Science Program, University of Maryland, College Park, Maryland, USA.
Department of Psychology, University of Maryland, College Park, Maryland, USA.

Junaid S Merchant (JS)

Neuroscience and Cognitive Science Program, University of Maryland, College Park, Maryland, USA.
Department of Psychology, University of Maryland, College Park, Maryland, USA.

Laura A Kirby (LA)

Department of Psychology, University of Maryland, College Park, Maryland, USA.

Heather A Yarger (HA)

Neuroscience and Cognitive Science Program, University of Maryland, College Park, Maryland, USA.
Department of Psychology, University of Maryland, College Park, Maryland, USA.

Elizabeth Redcay (E)

Neuroscience and Cognitive Science Program, University of Maryland, College Park, Maryland, USA.
Department of Psychology, University of Maryland, College Park, Maryland, USA.

Classifications MeSH