Neuroimaging the Effectiveness of Substance Use Disorder Treatments

J Neuroimmune Pharmacol. 2016 Sep;11(3):408-33. doi: 10.1007/s11481-016-9680-y. Epub 2016 May 16.

Abstract

Neuroimaging techniques to measure the function and biochemistry of the human brain such as positron emission tomography (PET), proton magnetic resonance spectroscopy ((1)H MRS), and functional magnetic resonance imaging (fMRI), are powerful tools for assessing neurobiological mechanisms underlying the response to treatments in substance use disorders. Here, we review the neuroimaging literature on pharmacological and behavioral treatment in substance use disorder. We focus on neural effects of medications that reduce craving (e.g., naltrexone, bupropion hydrochloride, baclofen, methadone, varenicline) and that improve cognitive control (e.g., modafinil, N-acetylcysteine), of behavioral treatments for substance use disorders (e.g., cognitive bias modification training, virtual reality, motivational interventions) and neuromodulatory interventions such as neurofeedback and transcranial magnetic stimulation. A consistent finding for the effectiveness of therapeutic interventions identifies the improvement of executive control networks and the dampening of limbic activation, highlighting their values as targets for therapeutic interventions in substance use disorders.

Keywords: Addiction; MRI; Neuroimaging; PET; Substance use disorder; Treatment.

Publication types

  • Review

MeSH terms

  • Clinical Trials as Topic / methods
  • Cognitive Behavioral Therapy / methods
  • Cognitive Behavioral Therapy / trends
  • Craving / drug effects
  • Craving / physiology
  • Humans
  • Methadone / pharmacology
  • Methadone / therapeutic use
  • Naltrexone / pharmacology
  • Naltrexone / therapeutic use
  • Neurofeedback / drug effects
  • Neurofeedback / methods
  • Neurofeedback / physiology
  • Neuroimaging / methods*
  • Neuroimaging / trends
  • Substance-Related Disorders / diagnostic imaging*
  • Substance-Related Disorders / therapy*
  • Treatment Outcome

Substances

  • Naltrexone
  • Methadone