[No association of 141C-ins/del polymorphism in the D2 dopamine receptor gene in schizophrenia]

Psychiatr Prax. 2003 May:30 Suppl 2:S212-5.
[Article in German]

Abstract

Recently, a putative functional polymorphism (-141C Ins/Del) in the 5'-flanking region of the dopamine D2 receptor was found. An association of the Ins allele with schizophrenia has been described in a Japanese sample. In the present study this association was examined in a German schizophrenia patient population. In a family based approach 190 German family trios were analyzed for the -141C Ins/Del genotype. Using the transmission disequilibrium test (TDT) we found no evidence for an association of the Ins allele with schizophrenia (TDT = 0.152, P = 0.696). In parallel, we performed an independent case control study with 268 schizophrenic patients and 244 controls. Again, we did not detect an overrepresentation of the Ins allele in patients (P = 0.124). Thus, our data do not support the hypothesis that the -141C Ins variant plays a major role in predisposition to schizophrenia. To confirm our conclusion further preferentially family based studies are needed.

Publication types

  • English Abstract

MeSH terms

  • Adult
  • Alleles
  • Case-Control Studies
  • Chromosome Deletion*
  • DNA Mutational Analysis
  • Female
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Linkage Disequilibrium / genetics
  • Male
  • Middle Aged
  • Mutagenesis, Insertional*
  • Polymorphism, Genetic / genetics*
  • Promoter Regions, Genetic / genetics
  • Receptors, Dopamine D2 / genetics*
  • Risk
  • Schizophrenia / genetics*

Substances

  • Receptors, Dopamine D2