CD38 polymorphisms in Spanish patients with systemic lupus erythematosus

被引:15
作者
González-Escribano, MF
Aguilar, F
Torres, B
Sánchez-Román, J
Núñez-Roldán, A
机构
[1] Hosp Univ Virgen del Rocio, Serv Immunol, Serv Andaluz Salud, Seville 41013, Spain
[2] Hosp Univ Virgen del Rocio, Unidad Colagenosis, Serv Andaluz Salud, Seville 41013, Spain
关键词
CD38; systemic lupus erythematosus-1; genetic susceptibility; genetic polymorphism;
D O I
10.1016/j.humimm.2004.02.032
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 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase (CD38) gene is a positional and functional candidate gene for the susceptibility to systemic lupus erythematosus (SLE) because CD38 gene maps in the described SLE risk region 4p15 and CD38 molecule is a leukocyte activation antigen and ectoenzyme involved in numerous immune functions. The aim of this study was to investigate the possible association of the polymorphisms located at positions 182 of intron I (C/G) and 418 (C/T, located in exon 3) of the CD38 gene with the susceptibility and clinical features of SLE. Genotyping of 276 Spanish patients with SLE and 194 controls was performed by polymerase chain reaction amplification-refractory mutation system techniques. No association between the polymorphisms studied and the susceptibility to SLE was found. However, when patients were stratified according to their clinical manifestations, a significant increase of CC individuals and a significant decrease of CG individuals among patients with discoid rash (67.996 vs. 53.1% in controls p = 0.02, p, > 0.05, odds ratio [OR] = 1.87, 95176 confidence interval [9596 CI] 1.05-3-35; and 23.5% vs. 40.2% in controls, p = 0.008, p, = 0.024, OR = 0.46 95% CI 0.24-0.85) were found. Logistic regression analysis identified CC genotype as an independent risk factor for discoid rash among patients with SLE (p = 0.01, OR = 2.23, 95% CI 1.19-4.18). In conclusion, a slight contribution of the polymorphism located in intron I of the CD38 gene in the clinical features of SLE could be postulated. (C) American Society for Histocompatibility and Immunogenetics, 2004. Published by Elsevier Inc.
引用
收藏
页码:660 / 664
页数:5
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