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克罗地亚南部人群中维生素D受体基因多态性与1型糖尿病的家系分析。

Family-based analysis of vitamin D receptor gene polymorphisms and type 1 diabetes in the population of South Croatia.

作者信息

Boraska Vesna, Škrabić Veselin, Zeggini Eleftheria, Groves Christopher James, Buljubašić Maja, Peruzović Marijana, Zemunik Tatijana

机构信息

Department of Medical Biology, Medical School, University of Split, 21000, Split, Croatia.

Department of Pediatrics, Clinical Hospital Split, 21000, Split, Croatia.

出版信息

J Hum Genet. 2008;53(3):210-214. doi: 10.1007/s10038-007-0234-2. Epub 2007 Dec 27.

Abstract

Type 1 diabetes mellitus (T1DM) is a disease characterised by the autoimmune destruction of insulin-producing pancreatic beta cells. Vitamin D is a known immune system modulator and its effects are exerted via the vitamin D receptor (VDR). Several VDR gene single nucleotide polymorphisms (SNPs) have been commonly studied in relation to T1DM. The aim of this study was to evaluate the role of VDR gene variation in T1DM susceptibility by genotyping four SNPs (FokI-rs10735810, TaqI-rs731236, BsmI-rs1544410, and Tru9I-rs757343) in 160 case-parent trio samples from the population of South Croatia. We observed overtransmission of Tru9I allele G and undertransmission of the Tru9I-BsmI A-A haplotype from parents to affected children (P = 0.032, P = 0.002, respectively). These results indicate a possible role of the VDR gene in T1DM aetiology. In conclusion, this family-based study presents some evidence of association of specific VDR gene variants with T1DM in the population of South Croatia.

摘要

1型糖尿病(T1DM)是一种以胰岛素分泌胰腺β细胞的自身免疫性破坏为特征的疾病。维生素D是一种已知的免疫系统调节剂,其作用通过维生素D受体(VDR)发挥。几种VDR基因单核苷酸多态性(SNP)已被普遍研究与T1DM的关系。本研究的目的是通过对来自克罗地亚南部人群的160个病例-父母三联体样本中的四个SNP(FokI-rs10735810、TaqI-rs731236、BsmI-rs1544410和Tru9I-rs757343)进行基因分型,评估VDR基因变异在T1DM易感性中的作用。我们观察到Tru9I等位基因G从父母向患病子女的过度传递以及Tru9I-BsmI A-A单倍型的传递不足(分别为P = 0.032,P = 0.002)。这些结果表明VDR基因在T1DM病因学中可能起作用。总之,这项基于家庭的研究提供了一些证据,证明特定的VDR基因变异与克罗地亚南部人群的T1DM有关。

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