C957T DRD2 polymorphism is associated with schizophrenia in Spanish patients

Acta Psychiatr Scand. 2006 Dec;114(6):435-8. doi: 10.1111/j.1600-0447.2006.00874.x.

Abstract

Objective: The objective was to confirm whether a homozygous genotype for the C957 allele of the C957T DRD2 gene single nucleotide polymorphism (SNP) is associated with schizophrenia in an independent study population.

Method: We examined the genotypic distribution of this SNP in a set of clinically ascertained schizophrenic patients (n = 131) and age-matched control subjects (n = 364). Individuals were genotyped using automated analysis of fluorescently labeled PCR products.

Results: The distribution of grouped genotypes for the C957T DRD2 SNP (CC vs. CT, TT) showed that C homozygote genotype was over-represented in our patient sample when compared with control subjects. This difference reaches the statistical significance (chi(2) = 7.0; df = 1; P = 0.008; OR = 2.05; % CI 1.2-3.4).

Conclusion: The findings of this study provide additional evidence that genetic variation at the DRD2 gene plays an important role in the vulnerability to schizophrenia.

MeSH terms

  • Adult
  • Alleles*
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease / genetics
  • Genetic Variation / genetics
  • Genotype*
  • Homozygote
  • Humans
  • Male
  • Polymorphism, Single Nucleotide / genetics*
  • Receptors, Dopamine D2 / genetics*
  • Risk Factors
  • Schizophrenia / diagnosis
  • Schizophrenia / genetics*
  • Spain

Substances

  • Receptors, Dopamine D2