Vitamin D receptor (VDR) gene polymorphisms and susceptibility to systemic lupus erythematosus clinical manifestations

被引:20
作者
de Azevedo Silva, J. [1 ,2 ]
Monteiro Fernandes, K. [2 ]
Tres Pancotto, J. A. [3 ]
Sotero Fragoso, T. [2 ]
Donadi, E. A. [4 ]
Crovella, S. [1 ,2 ]
Sandrin-Garcia, P. [1 ,2 ]
机构
[1] Univ Fed Pernambuco, Dept Genet, BR-50760901 Recife, PE, Brazil
[2] Univ Fed Pernambuco, Lab Immunopathol Keizo Asami LIKA, BR-50760901 Recife, PE, Brazil
[3] Fed Univ Espirito Santo UFES, Vitoria, ES, Brazil
[4] Univ Sao Paulo, Sch Med Ribeirao Preto, Dept Med, Div Clin Immunol, BR-05508 Sao Paulo, Brazil
关键词
SNPs; VDR gene; SLE; SLE clinical manifestations; TYPE-1; DIABETES-MELLITUS; D DEFICIENCY; ASSOCIATION; SLE; PREVALENCE; PROFILES; PROTECTS; CANCER; DAMAGE; BSMI;
D O I
10.1177/0961203313500549
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Systemic lupus erythematosus (SLE) is an autoimmune disorder with heterogeneous clinical manifestations and target tissue damage. Currently, several genes have been associated with SLE susceptibility, including vitamin D receptor (VDR), which is a mediator of immune responses through the action of vitamin D. Polymorphisms in the VDR gene can impair the vitamin D (D-3) function role, and since SLE patients show deficient D-3 blood levels, it leads to a possible connection to the disease's onset. In our study we searched for an association between VDR polymorphisms and risk of developing SLE, as well as the disease's clinical manifestations. We enrolled 158 SLE patients and 190 Southeast Brazilian healthy controls, genotyped for five Tag single nucleotide polymorphisms (SNPs), covering most of the VDR gene region. We found an association between VDR SNPs and SLE for the following clinical manifestations: rs11168268 and cutaneous alterations (p=0.036), rs3890733 (p=0.003) rs3890733 and arthritis (p=0.001), rs2248098 and immunological alterations (p=0.040), rs4760648 and antibody anti-dsDNA (p=0.036). No association was reported between VDR polymorphisms and SLE susceptibility.
引用
收藏
页码:1110 / 1117
页数:8
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