Lack of association between debrisoquine 4-hydroxylase (CYP2D6) gene polymorphisms and schizophrenia

Psychiatr Genet. 1998 Spring;8(1):25-8. doi: 10.1097/00041444-199800810-00004.

Abstract

Debrisoquine 4-hydroxylase (CYP2D6) is a cytochrome P450 enzyme involved in the metabolism of most neuroleptics, which are the drugs of choice for the treatment of psychotic symptoms. CYP2D6 in the brain was suggested to be functionally similar to the dopamine transporter, thus possibly influencing a neurotransmitter system involved in schizophrenia. Swedish schizophrenic patients (n = 124) and control individuals (n = 85) were investigated for two CYP2D6 polymorphisms, responsible for approximately 90% of mutations leading to poor debrisoquine metabolism. No significant CYP2D6 allele or genotype difference was found between schizophrenic patients and control individuals. Taken together with previous results, no major effect appears to be caused by the CYP2D6 gene on schizophrenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Brain / enzymology*
  • Chromosome Mapping
  • Cytochrome P-450 CYP2D6 / genetics*
  • Cytochrome P-450 CYP2D6 / metabolism
  • Humans
  • Mutation
  • Polymorphism, Genetic*
  • Reference Values
  • Schizophrenia / enzymology
  • Schizophrenia / genetics*
  • Sweden

Substances

  • Cytochrome P-450 CYP2D6