Adolescent impulsivity phenotypes characterized by distinct brain networks

Nat Neurosci. 2012 Jun;15(6):920-5. doi: 10.1038/nn.3092.

Abstract

The impulsive behavior that is often characteristic of adolescence may reflect underlying neurodevelopmental processes. Moreover, impulsivity is a multi-dimensional construct, and it is plausible that distinct brain networks contribute to its different cognitive, clinical and behavioral aspects. As these networks have not yet been described, we identified distinct cortical and subcortical networks underlying successful inhibitions and inhibition failures in a large sample (n = 1,896) of 14-year-old adolescents. Different networks were associated with drug use (n = 1,593) and attention-deficit hyperactivity disorder symptoms (n = 342). Hypofunctioning of a specific orbitofrontal cortical network was associated with likelihood of initiating drug use in early adolescence. Right inferior frontal activity was related to the speed of the inhibition process (n = 826) and use of illegal substances and associated with genetic variation in a norepinephrine transporter gene (n = 819). Our results indicate that both neural endophenotypes and genetic variation give rise to the various manifestations of impulsive behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Attention Deficit Disorder with Hyperactivity / genetics
  • Attention Deficit Disorder with Hyperactivity / physiopathology
  • Brain / physiology*
  • Brain Mapping*
  • Factor Analysis, Statistical
  • Female
  • Humans
  • Image Interpretation, Computer-Assisted
  • Impulsive Behavior / genetics
  • Impulsive Behavior / physiopathology*
  • Magnetic Resonance Imaging
  • Male
  • Nerve Net / physiology*
  • Norepinephrine Plasma Membrane Transport Proteins / genetics
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Substance-Related Disorders / genetics
  • Substance-Related Disorders / physiopathology

Substances

  • Norepinephrine Plasma Membrane Transport Proteins
  • SLC6A2 protein, human