No association of the Ser/Cys311 DRD2 molecular variant with schizophrenia using a classical case control study and the haplotype relative risk

Schizophr Res. 1997 May 24;25(2):117-21. doi: 10.1016/S0920-9964(97)00013-3.

Abstract

Arinami et al. (1994) reported an association between the Ser311/Cys311 variant of the DRD2 gene and schizophrenia in a Japanese population. We did not find statistically significant differences in the distribution of the allele frequencies between schizophrenics (103) and controls (97) in a case-control sample (chi 2 = 2.07; p = 0.150) or in 64 nuclear families with the haplotype relative risk (HRR) design (chi 2 = 0.13; p = 0.718). Our results seem to exclude a main involvement of this variant of the dopamine D2 receptor gene in the etiopathogenesis of schizophrenia.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Alleles
  • DNA / analysis
  • Female
  • Genotype
  • Haplotypes / genetics*
  • Humans
  • Male
  • Receptors, Dopamine D2 / genetics*
  • Schizophrenia / genetics*

Substances

  • Receptors, Dopamine D2
  • DNA