Korean J Lab Med.  2004 Dec;24(6):446-451.

Association between Schizophrenia and the Genetic Polymorphism of DRD3, DRD4 and HTR2A

Affiliations
  • 1Department of Neuropsychiatry, College of Medicine, Ewha Womans University, Seoul, Korea.
  • 2Department of Psychiatry, College of Medicine, University of Ulsan, Asan Medical Center, Seoul, Korea. jooyh@amc.seoul.kr
  • 3Department of Laboratory Medicine, College of Medicine, University of Ulsan, Asan Medical Center, Seoul, Korea.
  • 4Department of Statistics, Dongguk University, Seoul, Kroea.
  • 5Institute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul, Korea.

Abstract

BACKGROUND
Dopamine and serotonin receptors are candidate genes for the genetic study of schizophrenia because of their implication in the pathophysiology and etiology of schizophrenia (serotonine- dopamin hypothesis). A population-based association study was performed between schizophrenics and normal controls to identify the susceptibility genes. METHODS: A total of 145 schizophrenics and 242 normal controls were recruited. Ser9Gly polymorphism of DRD3, 12 bp repeat of DRD4, and 102T/C of HTR2A were selected as candidate polymorphism. The molecular techniques such as polymerase chain reaction (PCR)-restriction fragment length polymorphism and PCR-polyacrylamide gel electrophoresis were used. Chi-square analysis was performed to find any differences between two groups and logistic linear regression was tested to evaluate the interaction between three genes. RESULTS: There were no significant differences in allele frequencies and genotype frequencies of the three genetic polymorphism. Stratified by sex, the difference of DRD4 allele (P=0.065) and HTR2A allele (P=0.083) and genotype (P=0.054) was observed between male patients and controls; also noted was the difference of HTR2A genotype (P=0.080) between female patients and controls. Stratified by age of onset, the difference in the linear trend of DRD3 between early-onset patients and normal control (P=0.003) was observed. Stratified by family history, the difference in the linear trend of DRD4 (P=0.008) was also observed. Logistic linear regression with 90 patients who had early-onset phenotype (< or =20 year-old) or family history showed a significant result in interaction term (P=0.053). CONCLUSIONS: The finding that there were significant results only after stratification may imply a different genetic load on each subgroup of the disease. The interaction of genes between DRD3, DRD4, and HTR2A in a subgroup with supposedly high genetic background may support the serotonindopamine hypothesis. This, however, should be verified hereafter in large-scale studies.

Keyword

Schizophrenia; DRD3; DRD4; HTR2A; Association study; Gene interaction

MeSH Terms

Age of Onset
Alleles
Dopamine
Electrophoresis
Female
Gene Frequency
Genetic Load
Genotype
Humans
Linear Models
Male
Phenotype
Polymerase Chain Reaction
Polymorphism, Genetic*
Receptors, Serotonin
Schizophrenia*
Dopamine
Receptors, Serotonin
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