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乌拉圭人群中维生素D受体基因多态性的患病率及其与1型糖尿病的关系。

Prevalence of vitamin D receptor gene polymorphism in a Uruguayan population and its relation to type 1 diabetes mellitus.

作者信息

Mimbacas A, Trujillo J, Gascue C, Javiel G, Cardoso H

机构信息

Departamento de Citogenética, Unidad Asociada Instituto de Biología, Facultad de Ciencias, Montevideo, Uruguay.

出版信息

Genet Mol Res. 2007 Sep 5;6(3):534-42.

Abstract

Vitamin D has important immuno-modulatory properties and it influences insulin secretion. It acts through a vitamin D receptor (VDR), for which several gene polymorphisms have been described. The Uruguayan population presents several epidemiological characteristics that make it different from that of other counties, including other Latin-American countries. It went through miscegenation processes, with a tri-hybrid European, Amerindian and African origin, with no contribution from isolated Amerindian communities. Such differences have important consequences for the relationship between frequencies of several genes in the general population and their association with the diabetes mellitus. We examined the prevalence of VDR gene polymorphisms in the general population and their relation to type 1 diabetes in a parent-case design. One hundred unrelated individuals from the general population and 45 parent-patient triads with a child affected with type 1 diabetes were genotyped for FokI, BsmI and TaqI VDR gene polymorphisms by RFLP-PCR. We used a transmission disequilibrium test to assess preferential transmission of parents to affected offspring. The prevalence of the three VDR polymorphisms was: allele F = 48%, B = 35%, T = 64%. The f, b, T alleles and heterozygous genotypes were found at a high frequency in this population. Among 36 informative heterozygous parental genotypes, 30 transmitted the F allele (probability of transmission = 83%). The other two polymorphisms did not show significant transmission. We suggest that FokI polymorphism indicates susceptibility to type 1 diabetes mellitus in the Uruguayan population.

摘要

维生素D具有重要的免疫调节特性,并且会影响胰岛素分泌。它通过维生素D受体(VDR)发挥作用,针对该受体已描述了几种基因多态性。乌拉圭人群呈现出一些流行病学特征,使其与其他国家(包括其他拉丁美洲国家)的人群有所不同。它经历了混血过程,起源于欧洲、美洲印第安人和非洲人的三杂交,没有孤立的美洲印第安人群体的贡献。这些差异对于普通人群中几种基因的频率及其与糖尿病的关联之间的关系具有重要影响。我们在一项病例对照设计中研究了普通人群中VDR基因多态性的患病率及其与1型糖尿病的关系。通过RFLP-PCR对来自普通人群的100名无关个体和45个有1型糖尿病患儿的亲子三联体进行FokI、BsmI和TaqI VDR基因多态性的基因分型。我们使用传递不平衡检验来评估父母向受影响后代的优先传递情况。三种VDR多态性的患病率分别为:等位基因F = 48%,B = 35%,T = 64%。f、b、T等位基因和杂合基因型在该人群中发现频率较高。在36个信息丰富的杂合亲本基因型中,30个传递了F等位基因(传递概率 = 83%)。其他两种多态性未显示出显著的传递。我们认为FokI多态性表明乌拉圭人群对1型糖尿病易感性。

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