Association Study of the Sequence Mutation(T978C) of the Dopamine D5 Receptor Gene in Korean Schizophrenics / 신경정신의학
Journal of Korean Neuropsychiatric Association
; : 399-407, 1999.
Article
en Ko
| WPRIM
| ID: wpr-118575
Biblioteca responsable:
WPRO
ABSTRACT
OBJECTIVE: This study was performed to assess the possible involvement of the dopamine D5 receptor gene(DRD5) in the etiology of schizophrenia. METHODS: We identified the distribution of the T978C varient of the dopamine D5 receptor gene in 100 schizophrenics and 100 normal controls in Korean population, and evaluated the association between two groups. RESULTS: There were no significant differences in genotype frequency of T978C variation and genotype prevalence of homozygotes between schizophrenic and control groups. There was no significant difference in T978C allele frequencies between schizophrenic and control groups. CONCLUSION: We present evidence of a lack of allelic association between the exonic common polymorphism of the dopamine D5 receptor gene and Korean schizophrenic patients. The assumption that the T978C varient of the dopamine D5 receptor gene has a genetic role in the development of schizophrenia was not examined by this case-control study. However, because it is considered that DRD5 may act as the expression factor for the symptoms of schizophrenia or affect the difference in an individual's susceptibility to the disease, future studies to investigate the influence of other variations of DRD5 are needed.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Esquizofrenia
/
Dopamina
/
Estudios de Casos y Controles
/
Exones
/
Prevalencia
/
Receptores de Dopamina D5
/
Frecuencia de los Genes
/
Genotipo
/
Homocigoto
Tipo de estudio:
Observational_studies
/
Prevalence_studies
/
Prognostic_studies
/
Risk_factors_studies
Límite:
Humans
Idioma:
Ko
Revista:
Journal of Korean Neuropsychiatric Association
Año:
1999
Tipo del documento:
Article