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Association of MDR1 gene polymorphisms with refractory epilepsy in children / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 1073-1076, 2019.
Artigo em Chinês | WPRIM | ID: wpr-776744
ABSTRACT
OBJECTIVE@#To assess the association of single nucleotide polymorphisms of multidrug resistance gene 1 (MDR1) with refractory epilepsy in children.@*METHODS@#Peripheral blood samples were collected from 200 children with epilepsy and 100 healthy controls. Genomic DNA was extracted and subjected to PCR amplification, agarose gel electrophoresis and target site sequencing. Genotypes of rs1922242, rs2235048, rs10808072, rs868755 and rs1202184 loci of the MDR1 gene were analyzed.@*RESULTS@#No significant difference was found in genotypic distribution and allelic frequencies of the rs1922242, rs2235048, rs10808072 and rs868755 loci between the drug-resistant and drug-sensitive groups. For the rs1202184 locus, a significant difference in genotypic distribution was found (P=0.008). No significant difference was found in the frequencies of various haplotypes between the two groups.@*CONCLUSION@#Genotypes of the rs1202184 locus of the MDR1 gene are associated with refractory epilepsy in children, for which the AA genotype plays a dominant role.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Haplótipos / Estudos de Casos e Controles / Subfamília B de Transportador de Cassetes de Ligação de ATP / Polimorfismo de Nucleotídeo Único / Epilepsia Resistente a Medicamentos / Frequência do Gene / Genética / Genótipo Tipo de estudo: Estudo observacional / Fatores de risco Limite: Criança / Humanos Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2019 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Haplótipos / Estudos de Casos e Controles / Subfamília B de Transportador de Cassetes de Ligação de ATP / Polimorfismo de Nucleotídeo Único / Epilepsia Resistente a Medicamentos / Frequência do Gene / Genética / Genótipo Tipo de estudo: Estudo observacional / Fatores de risco Limite: Criança / Humanos Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2019 Tipo de documento: Artigo