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Association of Common Genetic Variants in Mitogen-activated Protein Kinase Kinase Kinase Kinase 4 with Type 2 Diabetes Mellitus in a Chinese Han Population / 中华医学杂志(英文版)
Chinese Medical Journal ; (24): 1179-1184, 2016.
Article em En | WPRIM | ID: wpr-290105
Biblioteca responsável: WPRO
ABSTRACT
<p><b>BACKGROUND</b>A study has identified several novel susceptibility variants of the mitogen-activated protein kinase kinase kinase kinase 4 (MAP4K4) gene for type 2 diabetes mellitus (T2DM) within the German population. Among the variants, five single nucleotide polymorphisms (SNPs) of MAP4K4 (rs1003376, rs11674694, rs2236935, rs2236936, and rs6543087) showed significant association with T2DM or diabetes-related quantitative traits. We aimed to evaluate whether common SNPs in the MAP4K4 gene were associated with T2DM in the Chinese population.</p><p><b>METHODS</b>Five candidate SNPs were genotyped in 996 patients newly diagnosed with T2DM and in 976 control subjects, using the SNPscan™ method. All subjects were recruited from the Second Affiliated Hospital, Harbin Medical University from October 2010 to September 2013. We evaluated the T2DM risk conferred by individual SNPs and haplotypes using logistic analysis, and the association between the five SNPs and metabolic traits in the subgroups.</p><p><b>RESULTS</b>Of the five variants, SNP rs2236935T/C was significantly associated with T2DM in this study population (odds ratio = 1.293; 95% confidence interval: 1.034-1.619, P= 0.025). In addition, among the controls, rs1003376 was significantly associated with an increased body mass index (P = 0.045) and homeostatic model assessment-insulin resistance (P = 0.037).</p><p><b>CONCLUSIONS</b>MAP4K4 gene is associated with T2DM in a Chinese Han population, and MAP4K4 gene variants may contribute to the risk toward the development of T2DM.</p>
Assuntos
Texto completo: 1 Índice: WPRIM Assunto principal: Haplótipos / Desequilíbrio de Ligação / Proteínas Serina-Treonina Quinases / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Povo Asiático / Peptídeos e Proteínas de Sinalização Intracelular / Diabetes Mellitus Tipo 2 / Genética / Genótipo Limite: Adult / Female / Humans / Male Idioma: En Revista: Chinese Medical Journal Ano de publicação: 2016 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Haplótipos / Desequilíbrio de Ligação / Proteínas Serina-Treonina Quinases / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Povo Asiático / Peptídeos e Proteínas de Sinalização Intracelular / Diabetes Mellitus Tipo 2 / Genética / Genótipo Limite: Adult / Female / Humans / Male Idioma: En Revista: Chinese Medical Journal Ano de publicação: 2016 Tipo de documento: Article