Tumor necrosis factor-alpha-308 promoter polymorphism contributes independently to HLA alleles in the severity of rheumatoid arthritis in Mexicans

被引:52
|
作者
Rodríguez-Carreón, AA
Zúñiga, J
Hernández-Pacheco, G
Rodríguez-Pérez, JM
Pérez-Hernández, N
de Oca, JVM
Cardiel, MH
Granados, J
Vargas-Alarcón, G
机构
[1] Inst Nacl Cardiol Ignacio Chavez, Dept Physiol, Mexico City, DF, Mexico
[2] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Immunol & Rheumatol, Zubiran, Mexico
关键词
genetic susceptibility; HLA alleles; major histocompatibility complex; rheumatoid arthritis; tumor necrosis factor;
D O I
10.1016/j.jaut.2004.11.002
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 aim of this study was to determine the frequency and potential relevance of the promoter polymorphisms of the tumor necrosis factor-alpha (TNF-alpha) in the severity of rheumatoid arthritis (RA) in Mexicans. HLA-DR and polymorphisms at positions -238 and -308 of TNF-alpha gene were determined in 137 Mexican RA patients (44 with severe and 93 with non-severe RA) as well as in 169 healthy controls (99 were typed for HLA-DR). We observed an increased frequency of HLA-DR4 in severe RA compared to healthy controls (pC = 0.02, OR = 2.33). TNF polymorphism analysis showed a significant increased frequency of TNF -238 GG genotype in the whole group of RA patients when compared to healthy controls (pC = 0.007, OR = 4.71). When the analyses were carried out separately in severe and non-severe RA patients, the increased frequency of -238 GG genotype only was observed in patients with non-severe forms of the disease. Analysis of -308 polymorphism showed increased frequency of -308 T2 (A) allele in severe RA when compared to non-severe disease (pQ = 0.011, OR = 3.29) and to healthy controls (pC = 0.002, OR = 3.97). The data demonstrate that -308 T2 (A) allele is associated with susceptibility to develop severe RA in Mexicans. This association could be independent from HLA-DR alleles and might be used as a prognostic marker for severe RA. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:63 / 68
页数:6
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