Serotonergic gene variation in substance use pharmacotherapy: a systematic review

Pharmacogenomics. 2015;16(11):1307-14. doi: 10.2217/pgs.15.72. Epub 2015 Aug 12.

Abstract

Drug addiction is a serious disease with damaging effects on the brain and physical health. Despite the increase in the number of affected individuals, there are few effective pharmacological treatment options for substance use disorders. The study of the influence of an individual's genetic features on the treatment response may help to identify more efficacious treatment options. This systematic review focuses on the serotonergic system because of its relevant role in mood and impulse control disorders, and its contribution to the development and maintenance of drug use disorders. In particular, we examine the role of serotonergic genes in the response to pharmacotherapy for alcohol, cocaine and nicotine addiction. Current evidence suggests that genetic variability of the serotonergic biosynthesis enzyme tryptophan hydroxylase 2 (TPH2) and the serotonin transporter (SLC6A4) genes mediates the efficacy of several addiction treatments, such as ondansetron and disulfiram, and the antidepressants bupropion, nortriptyline and sertraline.

Keywords: addiction; bupropion; disulfiram; gene; ondansetron; serotonergic; sertraline; treatment.

Publication types

  • Meta-Analysis
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review
  • Systematic Review

MeSH terms

  • Genetic Variation
  • Humans
  • Serotonin / genetics*
  • Serotonin Agents / therapeutic use
  • Serotonin Plasma Membrane Transport Proteins / genetics
  • Substance-Related Disorders / drug therapy*
  • Tryptophan Hydroxylase / genetics

Substances

  • SLC6A4 protein, human
  • Serotonin Agents
  • Serotonin Plasma Membrane Transport Proteins
  • Serotonin
  • TPH2 protein, human
  • Tryptophan Hydroxylase