뚜렛증후군과 만성 틱장애 그리고 도파민 D2 수용체 유전자와의 연합 연구
Association Study between Tic Disorder and Dopamine D2 Receptor Gene Polymorphism in Korean Population
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Abstract
Objectives: The purpose of the present study was to investigate whether the TaqI A polymorphism of dopamine receptor D2 gene (DRD2) is associated with Tourette syndrome (TS) and chronic motor tic disorder (CMT) in Korean population. Methods: DRD2 TaqI A RFLP genotyping was carried out with DNA extracted from blood samples of 75 patients with tic disorders (47 with TS and 28 with CMT) and 90 healthy subjects. Genotype and allelic frequencies for the DRD2 gene polymorphisms of the tic disorder group as a whole were compared to those of the control group. Separating the TS group, thereafter, the frequency of genotypes and alleles were compared to those of the controls. Results: The results demonstrated that genotype and allele distributions for the DRD2 gene polymorphism in the tic disorder as a whole, TS, and control groups were not significantly different. Conclusion: No association was found for DRD2 gene, TS and CMT. The data suggest that DRD2 gene may not be a useful marker for the prediction of the susceptibility of tic disorder.
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