Pharmacogenetics in affective disorders

Eur J Pharmacol. 2002 Mar 8;438(3):117-28. doi: 10.1016/s0014-2999(02)01309-2.

Abstract

Pharmacogenetics will be of substantial help in the field of affective disorders pharmacotherapy. The possible definition of a genetic liability profile for drug side-effects and efficacy will be of great help in treatments that need weeks to months to be effective. During the last few years, a number of groups have reported possible liability genes. The efficacy and time of onset of selective serotonin reuptake inhibitors have been associated with a polymorphism in the promoter region of the transporter (SERTPR) in many independent studies, while variants at the tryptophan hydroxylase gene, 5-HT2a receptor and G-protein beta3 have been associated with them in pilot studies. Lithium long-term prophylactic efficacy has been associated with SERTPR, TPH and inositol polyphosphate 1-phosphatase variants, though in unreplicated samples. A number of further candidate genes were not associated with these treatments. In conclusion, both acute and long-term treatments appear to be, at least to some extent, under genetic influence and preliminary data have identified possible liability genes.

Publication types

  • Review

MeSH terms

  • Animals
  • Antidepressive Agents / therapeutic use
  • Antipsychotic Agents / therapeutic use
  • Carrier Proteins / genetics
  • GTP-Binding Proteins / genetics
  • Genotype
  • Humans
  • Lithium / therapeutic use
  • Membrane Glycoproteins / genetics
  • Membrane Transport Proteins*
  • Mood Disorders / drug therapy*
  • Mood Disorders / genetics
  • Nerve Tissue Proteins*
  • Pharmacogenetics / methods*
  • Receptor, Serotonin, 5-HT2A
  • Receptors, Serotonin / genetics
  • Serotonin Plasma Membrane Transport Proteins

Substances

  • Antidepressive Agents
  • Antipsychotic Agents
  • Carrier Proteins
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • Receptor, Serotonin, 5-HT2A
  • Receptors, Serotonin
  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins
  • Lithium
  • GTP-Binding Proteins