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Association of schizophrenia with a promoter polymorphism in the dopamine D2 receptor gene / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 94-95, 2005.
Artículo en Chino | WPRIM | ID: wpr-321148
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the association of -141C insert/delete polymorphism with schizophrenia in Wuhan of Hubei province.</p><p><b>METHODS</b>A case-control study was conducted to analyze the polymorphism in the D(2) receptor gene promoter region with schizophrenia. A total of 120 cases of schizophrenia diagnosed according to CCMD-II R criteria and 100 normal controls were recruited in the study.</p><p><b>RESULTS</b>In this sample, the allele and genotype showed statistically significant differences between patients and normal controls (P<0.05).Especially, the frequency of -141C del was 11% in patients and 18% in control(OR 0.55, 95% CI 0.30-0.96; P<0.05). This allele was less common in schizophrenia than in normal controls (P<0.05).</p><p><b>CONCLUSION</b>The -141C del polymorphism is associated with schizophrenia.The polymorphism may modify the association with other factors. Possibly -141C del in the DRD(2) promoter region is a strong candidate for a protective factor for this trait.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Polimorfismo Genético / Esquizofrenia / Reacción en Cadena de la Polimerasa / Regiones Promotoras Genéticas / Receptores de Dopamina D2 / Diagnóstico / Alelos / Frecuencia de los Genes / Genética / Genotipo Tipo de estudio: Estudio diagnóstico / Estudio observacional Límite: Adulto / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2005 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Polimorfismo Genético / Esquizofrenia / Reacción en Cadena de la Polimerasa / Regiones Promotoras Genéticas / Receptores de Dopamina D2 / Diagnóstico / Alelos / Frecuencia de los Genes / Genética / Genotipo Tipo de estudio: Estudio diagnóstico / Estudio observacional Límite: Adulto / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2005 Tipo del documento: Artículo