Functional single-nucleotide polymorphisms in the DEFB1 gene are associated with systemic lupus erythematosus in Southern Brazilians


Autoria(s): Sandrin-Garcia, P.; Brandao, L. A. C.; Guimaraes, R. L.; Pancoto, J. A. T.; Donadi, E. A.; de Lima-Filho, J. L.; Segat, L.; Crovella, S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

12/10/2013

12/10/2013

2012

Resumo

Systemic lupus erythematosus (SLE) is an autoimmune disease that results in inflammation and tissue damage. The etiology of SLE remains unknown, but recent studies have shown that the innate immune system may have a role in SLE pathogenesis through the secretion of small cationic peptides named defensins. The aim of the study was to determine the possible involvement in SLE of three functional single nucleotide polymorphisms (SNPs) (c.-52G>A, c.-44C>G and c.-20G>A) in the 5'UTR region of DEFB1 gene, by analyzing them in a population of 139 SLE patients and 288 healthy controls. The c.-52G>A SNP showed significant differences in allele and genotype frequency distribution between SLE patients and controls (p = 0.01 and p = 0.02 respectively) indicating protection against SLE (A allele, OR = 0.68, AA genotype OR = 0.51). Significant differences were also observed for c.-44C>G SNP, the C/G genotype being associated with susceptibility to SLE (OR = 1.60, p = 0.04). Moreover, statistically significant differences between patients and controls were found for two DEFB1 haplotypes (GCA and GGG, p = 0.01 and p = 0.02 respectively). When considering DEFB1 SNPs and SLE clinical and laboratory manifestations, significant association was found with neuropsychiatric disorders, immunological alterations and anti-DNA antibodies. In conclusion, our results evidence a possible role for the c.-52G>A and c.-44C>G DEFB1 polymorphisms in SLE pathogenesis, that can be considered as possible risk factors for development of disease and disease-related clinical manifestations. Additional studies are needed, to corroborate these results as well as functional studies to understand the biological role of these SNPs in the pathogenesis of SLE. Lupus (2012) 21, 625-631.

FACEPE/CNPq

FACEPE/CNPq

FACEPE

FACEPE [APQ-0020-4.01/08]

European Project 'Talents for an International House'

European Project Talents for an International House

Identificador

LUPUS, LONDON, v. 21, n. 6, supl. 1, Part 1, pp. 625-631, MAY, 2012

0961-2033

http://www.producao.usp.br/handle/BDPI/34208

10.1177/0961203312436858

http://dx.doi.org/10.1177/0961203312436858

Idioma(s)

eng

Publicador

SAGE PUBLICATIONS LTD

LONDON

Relação

LUPUS

Direitos

closedAccess

Copyright SAGE PUBLICATIONS LTD

Palavras-Chave #SYSTEMIC LUPUS ERYTHEMATOSUS #SNPS #DEFB1 #GENETIC POLYMORPHISMS #DEFENSINS #HUMAN BETA-DEFENSIN-1 GENE #ATOPIC-DERMATITIS #BETA-DEFENSIN #HIV-1 INFECTION #CHILDREN #HAPLOTYPE #POPULATIONS #EXPRESSION #PEPTIDES #ASTHMA #RHEUMATOLOGY
Tipo

article

original article

publishedVersion