Macrophage migration inhibitory factor gene:: Influence on rheumatoid arthritis susceptibility

被引:50
|
作者
Martinez, Alfonso
Orozco, Gisela
Varade, Jezabel
Lopez, Marta Sanchez
Pascual, Dora
Balsa, Alejandro
Garcia, Antonio
de la Concha, Emilio G.
Fernandez-Gutierrez, Benjamin
Martin, Javier
Urcelay, Elena [1 ]
机构
[1] Hosp Clin San Carlos, Dept Clin Immunol, Madrid, Spain
[2] CSIC, Lopez Neyra Inst, Granada, Spain
[3] Hosp Clin San Carlos, Dept Rheumatol, Madrid, Spain
[4] Hosp La Paz, Dept Rheumatol, Madrid, Spain
[5] Hosp Virgen Nieves, Dept Rheumatol, Granada, Spain
关键词
MIF gene; rheumatoid arthritis; susceptibility; early-onset;
D O I
10.1016/j.humimm.2007.06.007
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 macrophage inhibitory factor (MIF) is a cytokine that has been implicated in several inflammatory and autoimmune diseases, including rheumatoid arthritis, systemic Lupus, glomerutonephritis, and multiple sclerosis. In rheumatoid arthritis (RA), results ranging from tack of association of MIF polymorphisms with RA, to involvement in either severity or suscep-tibitity to the disease have been reported in the past. We aimed at investigating the role of this gene in RA in the Spanish population. Two well-known MIF promoter polymorphisms were tested in 606 adult RA patients and 886 healthy controls: a single nucleotide polymorphism at - 1 73G/C and a tetranucleotide repeat (CATT)(5-8) located at -794. We found a significant association of the allele -173C with RA (p = 0.01; odds ratio [OR] = 1.31; 95% confidence interval [Cl] 1.06-1.62). The -173C risk allele, previously reported to be transmitted in excess in patients with juvenile idiopathic arthritis, was significantly more frequent in earty-onset adult RA patients than in healthy controls (p = 0.003; OR = 1.57; 95% Cl = 1.14-2.15), whereas late-onset patients were not significantly different to controls (p = 0.6; OR = 1.09; 95% Cl = 0.77-1.55). In conclusion, the -173C allele in the MIF promoter region is associated with increased RA predisposition, mainly in earty-onset patients. (C) 2007 American Society for Histocompatibitity and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:744 / 747
页数:4
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