[Risperidone intoxication in a patient with a genetic predisposition as "poor [non]metabolizer"]

Psychiatr Prax. 2010 May;37(4):199-201. doi: 10.1055/s-0029-1223511. Epub 2010 Mar 11.
[Article in German]

Abstract

Objective: The enzyme system cytochrome P450 plays a central role in the metabolism of drugs in the human body. The enzyme CYP2D6 is important for the metabolism of psychoactive agents. Genetic changes in the CYP2D6 gene can lead to reduced or absent activity.

Methods: We report on a 37-year-old female patient who was given risperidone to treat an acute delusional disorder. Despite receiving a very low dose, the patient suffered from an intoxication. We inferred that an excessively raised plasma level of risperidone may result from a pharmacologically relevant disorder of metabolism.

Results: The molecular genetic investigation revealed a compound heterozygous mutation in the CYP2D6 gene and thus documented a genetic predisposition as a "poor [non]metabolizer".

Conclusions: In intoxications with psychoactive agents, the presence of an enzyme defect in the P450 system should be considered as an additional possible cause.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antipsychotic Agents / pharmacokinetics*
  • Antipsychotic Agents / therapeutic use
  • Antipsychotic Agents / toxicity*
  • Chromosomes, Human, Pair 22 / genetics
  • Cyclohexanols / pharmacokinetics
  • Cyclohexanols / therapeutic use
  • Cytochrome P-450 CYP2D6 / genetics*
  • DNA Mutational Analysis
  • Delusions / blood
  • Delusions / drug therapy*
  • Delusions / genetics
  • Dose-Response Relationship, Drug
  • Drug Monitoring
  • Drug Therapy, Combination
  • Exons / genetics
  • Female
  • Genetic Carrier Screening
  • Humans
  • Inactivation, Metabolic / genetics
  • Introns / genetics
  • Metabolic Clearance Rate
  • Psychotic Disorders / blood
  • Psychotic Disorders / drug therapy*
  • Psychotic Disorders / genetics
  • Risperidone / pharmacokinetics*
  • Risperidone / therapeutic use
  • Risperidone / toxicity*
  • Selective Serotonin Reuptake Inhibitors / adverse effects
  • Selective Serotonin Reuptake Inhibitors / therapeutic use
  • Venlafaxine Hydrochloride

Substances

  • Antipsychotic Agents
  • Cyclohexanols
  • Serotonin Uptake Inhibitors
  • Venlafaxine Hydrochloride
  • Cytochrome P-450 CYP2D6
  • Risperidone