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Transmission disequilibrium analysis of 1137-1140 Del GTGA frameshift mutation within the KCNN3 gene and schizophrenia based on family trios / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 441-443, 2005.
Artículo en Chino | WPRIM | ID: wpr-280031
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the relationship between 1137-1140 Del GTGA in exon 1 at KCNN3 gene and schizophrenia.</p><p><b>METHODS</b>The study included 289 subjects (affected 107; unaffected 182) from 95 schizophrenic trios. All subjects were collected from Han Chinese in south China and genotyped for 1137-1140 Del GTGA in KCNN3 using PCR and restriction endonuclease Dde I. All the affected patients met the CCMD-II-R criteria for schizophrenia. The haplotype-based haplotype relative risk(HHRR) and transmission/disequilibrium test(TDT) analyses were done in 95 schizophrenic trios.</p><p><b>RESULTS</b>Comparative analysis on the distribution of alleles between the affected and unaffected parents(87 family trios) showed no significant difference(X(2)=0.253, P> 0.05). HHRR showed that KCNN3 gene alleles transmitted to the patients were not different from that of the non-transmitted parental alleles(X(2)=0.042, P> 0.05). TDT revealed that A(2) alleles were not preferentially transmitted to schizophrenic patients(X(2)=3.000, P=0.0833).</p><p><b>CONCLUSION</b>In this study a lower frequency for 1137-1140 Del homozygote of KCNN3 gene was observed, and the HHRR and TDT analyses suggested that the 1137-1140 Del alleles of KCNN3 gene be unlikely to confer susceptibility to schizophrenia.</p>
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Esquizofrenia / Haplotipos / Núcleo Familiar / Desequilibrio de Ligamiento / Salud de la Familia / Mutación del Sistema de Lectura / Predisposición Genética a la Enfermedad / Canales de Potasio de Pequeña Conductancia Activados por el Calcio / Genética Tipo de estudio: Estudio de etiología Límite: Adolescente / Adulto / Anciano / Niño / 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: Esquizofrenia / Haplotipos / Núcleo Familiar / Desequilibrio de Ligamiento / Salud de la Familia / Mutación del Sistema de Lectura / Predisposición Genética a la Enfermedad / Canales de Potasio de Pequeña Conductancia Activados por el Calcio / Genética Tipo de estudio: Estudio de etiología Límite: Adolescente / Adulto / Anciano / Niño / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2005 Tipo del documento: Artículo