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Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome in China / 浙江大学学报(英文版)(B辑:生物医学和生物技术)
Article em En | WPRIM | ID: wpr-277295
Biblioteca responsável: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To explore the relationship between genetic polymorphisms in methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase (MTRR), the central enzymes in folate metabolism that affects DNA methylation and synthesis, and the risk of Down syndrome in China.</p><p><b>METHODS</b>Genomic DNA was isolated from the peripheral lymphocytes of 64 mothers of children with Down syndrome and 70 age matched control subjects. Polymerase chain reaction and restriction fragment length polymorphism were used to examine the polymorphisms of MTHFR 677C-->T, MTRR 66A-->G and the relationship between these genotypes and the risk of Down syndrome was analyzed.</p><p><b>RESULTS</b>The results show that the MTHFR 677C-->T polymorphism is more prevalent among mothers of children with Down syndrome than among control mothers, with an odds ratio of 3.78 (95% confidence interval (CI), 1.78 approximately 8.47). In addition, the homozygous MTRR 66A-->G polymorphism was independently associated with a 5.2-fold increase in estimated risk (95% CI, 1.90 approximately 14.22). The combined presence of both polymorphisms was associated with a greater risk of Down syndrome than the presence of either alone, with an odds ratio of 6.0 (95% CI, 2.058 approximately 17.496). The two polymorphisms appear to act without a multiplicative interaction.</p><p><b>CONCLUSION</b>MTHFR and MTRR gene mutation alleles are related to Down syndrome, and CT, TT and GG gene mutation types increase the risk of Down syndrome.</p>
Assuntos
Texto completo: 1 Base de dados: WPRIM Assunto principal: Polimorfismo Genético / Linfócitos / Estudos de Casos e Controles / China / Fatores de Risco / Síndrome de Down / Predisposição Genética para Doença / Metilenotetra-Hidrofolato Redutase (NADPH2) / Diagnóstico / Alelos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans País/Região como assunto: Asia Idioma: En Revista: Journal of Zhejiang University. Science. B Ano de publicação: 2008 Tipo de documento: Article
Texto completo: 1 Base de dados: WPRIM Assunto principal: Polimorfismo Genético / Linfócitos / Estudos de Casos e Controles / China / Fatores de Risco / Síndrome de Down / Predisposição Genética para Doença / Metilenotetra-Hidrofolato Redutase (NADPH2) / Diagnóstico / Alelos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans País/Região como assunto: Asia Idioma: En Revista: Journal of Zhejiang University. Science. B Ano de publicação: 2008 Tipo de documento: Article