Corticostriatal responses to social reward are linked to trait reward sensitivity and subclinical substance use in young adults.


Journal

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

Informations de publication

Date de publication:
16 Mar 2024
Historique:
pubmed: 31 1 2023
medline: 31 1 2023
entrez: 30 1 2023
Statut: epublish

Résumé

Aberrant levels of reward sensitivity have been linked to substance use disorder and are characterized by alterations in reward processing in the ventral striatum (VS). Less is known about how reward sensitivity and subclinical substance use relate to striatal function during social rewards (e.g., positive peer feedback). Testing this relation is critical for predicting risk for development of substance use disorder. In this pre-registered study, participants (N=44) underwent fMRI while completing well-matched tasks that assess neural response to reward in social and monetary domains. Contrary to our hypotheses, aberrant reward sensitivity blunted the relationship between substance use and striatal activation during receipt of rewards, regardless of domain. Moreover, exploratory whole-brain analyses showed unique relations between substance use and social rewards in temporoparietal junction. Psychophysiological interactions demonstrated that aberrant reward sensitivity is associated with increased connectivity between the VS and ventromedial prefrontal cortex during social rewards. Finally, we found that substance use was associated with decreased connectivity between the VS and dorsomedial prefrontal cortex for social rewards, independent of reward sensitivity. These findings demonstrate nuanced relations between reward sensitivity and substance use, even among those without substance use disorder, and suggest altered reward-related engagement of cortico-VS responses as potential predictors of developing disordered behavior.

Identifiants

pubmed: 36711485
doi: 10.1101/2023.01.17.524305
pmc: PMC9882176
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIA NIH HHS
ID : RF1 AG067011
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH132727
Pays : United States
Organisme : NIDA NIH HHS
ID : R03 DA046733
Pays : United States
Organisme : NICHD NIH HHS
ID : R21 HD093912
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH126911
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH123473
Pays : United States

Auteurs

Classifications MeSH