Blunted ventral striatal responses to anticipated rewards foreshadow problematic drug use in novelty-seeking adolescents

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Universität Hamburg
  • Stanford University
  • Universität Heidelberg
  • Trinity College Dublin
  • King's College London (KCL)
  • University of Montreal
  • Commissariat à l’énergie atomique et aux énergies alternatives (CEA)
  • University of Vermont
  • University of Nottingham
  • Charité – Universitätsmedizin Berlin
  • Physikalisch-Technische Bundesanstalt
  • INSERM - Institut national de la santé et de la recherche médicale
  • Université Paris Cité
  • McGill University
  • University of Toronto
  • Centre Universitaire de Sante McGill
  • University of Cambridge
  • Medical Research Council (MRC)

Abstract

Novelty-seeking tendencies in adolescents may promote innovation as well as problematic impulsive behaviour, including drug abuse. Previous research has not clarified whether neural hyper- or hypo-responsiveness to anticipated rewards promotes vulnerability in these individuals. Here we use a longitudinal design to track 144 novelty-seeking adolescents at age 14 and 16 to determine whether neural activity in response to anticipated rewards predicts problematic drug use. We find that diminished BOLD activity in mesolimbic (ventral striatal and midbrain) and prefrontal cortical (dorsolateral prefrontal cortex) regions during reward anticipation at age 14 predicts problematic drug use at age 16. Lower psychometric conscientiousness and steeper discounting of future rewards at age 14 also predicts problematic drug use at age 16, but the neural responses independently predict more variance than psychometric measures. Together, these findings suggest that diminished neural responses to anticipated rewards in novelty-seeking adolescents may increase vulnerability to future problematic drug use.

Details

OriginalspracheEnglisch
Aufsatznummer14140
FachzeitschriftNature communications
Jahrgang8
PublikationsstatusVeröffentlicht - 21 Feb. 2017
Peer-Review-StatusJa

Externe IDs

PubMed 28221370
ORCID /0000-0001-5398-5569/work/161890769