Lack of association of vitamin D receptor gene polymorphisms with susceptibility to type 1 diabetes mellitus in the Portuguese population

被引:60
|
作者
Lemos, Manuel C. [1 ,2 ,3 ]
Fagulha, Ana [2 ]
Coutinho, Eduarda [3 ]
Gomes, Leonor [2 ]
Bastos, Margarida [2 ]
Barros, Luisa [2 ]
Carrilho, Francisco [2 ]
Geraldes, Elizabete [2 ]
Regateiro, Fernando J. [3 ]
Carvatheiro, Manuela [2 ]
机构
[1] Univ Beira Interior, Fac Hlth Sci, Hlth Sci Res Ctr CICS, P-6200506 Covilha, Portugal
[2] Univ Hosp Coimbra, Endocrinol Diabet & Metab Serv, P-3000075 Coimbra, Portugal
[3] Univ Coimbra, Fac Med, Gen Med Serv, P-3004504 Coimbra, Portugal
关键词
vitamin D receptor; VDR; single nucleotide polymorphism; SNP; type 1 diabetes mellitus; genetic susceptibility;
D O I
10.1016/j.humimm.2008.01.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The vitamin D receptor (VDR) gene is a candidate gene for susceptibility to autoimmune disorders. Association studies of VDR polymorphisms and risk of type 1 diabetes often produced conflicting results in different ethnic backgrounds. The aim of this study was to test for association between common VDR polymorphisms and the genetic susceptibility to type I diabetes in the Portuguese population. We genotyped 207 patients with type 1 diabetes and 249 controls for the FokI T>C (rs10735810), BsmI A>G (rs1544410), Apal G>T (rs7975232), and Taql C>T (rs731236) single nucleotide polymorphisms by polymerase chain reaction and restriction fragment Length polymorphism analysis. The distribution of VDR genotype, allele, and haplotype frequencies did not differ significantly between patients and controls. These data suggest that the single nucleotide polymorphisms of the VDR gene are unlikely to contribute significantly to type 1 diabetes susceptibility in the Portuguese population. (C) 2008 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:134 / 138
页数:5
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