Breaking barriers in the genomics and pharmacogenetics of drug addiction

Clin Pharmacol Ther. 2010 Dec;88(6):779-91. doi: 10.1038/clpt.2010.175. Epub 2010 Oct 27.

Abstract

Drug addiction remains a substantial health issue with limited treatment options currently available. Despite considerable advances in the understanding of human genetic architecture, the genetic underpinning of complex disorders remains elusive. On the basis of our current understanding of neurobiology, numerous candidate genes have been implicated in the etiology and response to treatment for different addictions. Genome-wide association (GWA) studies have also identified novel targets. However, replication of these studies is often lacking, and this complicates interpretation. The situation is expected to improve as issues such as phenotypic characterization, the apparent "missing heritability," the identification of functional variants, and possible gene-environment (G × E) interactions are addressed. In addition, there is growing evidence that genetic information can be useful in refining the choice of addiction treatment. As genetic testing becomes more common in the practice of medicine, a variety of ethical and practical challenges, some of which are unique to drug addiction, will also need to be considered.

Publication types

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

MeSH terms

  • Genetic Testing / methods
  • Genetic Testing / trends
  • Genetic Variation / genetics
  • Genomics / methods*
  • Genomics / trends
  • Humans
  • Methadone / therapeutic use
  • Naltrexone / therapeutic use
  • Pharmacogenetics / methods*
  • Pharmacogenetics / trends
  • Substance-Related Disorders / diagnosis
  • Substance-Related Disorders / drug therapy*
  • Substance-Related Disorders / genetics*

Substances

  • Naltrexone
  • Methadone