Contribution of HLA class II genes to end stage renal disease in Mexican patients with type 2 diabetes mellitus

被引:26
作者
Pérez-Luque, E
Malacara, JM
Olivo-Díaz, A
Aláez, C
Debaz, H
Vázquez-Garcia, M
Garay, ME
Nava, LE
Burguete, A
Gorodezky, C
机构
[1] Inst Diagnost & Referencia Epidemiol, InDRE SSA, Dept Immunogenet, Mexico City 11340, DF, Mexico
[2] Univ Guanajuato, Inst Invest Med, Leon, Gto, Mexico
[3] IPN, CINVESTAV, Program Mol Biomed, Mexico City 07738, DF, Mexico
[4] Inst Mexicano Suguro Social, Leon, Gto, Mexico
关键词
end stage renal disease; type; 2; DM; class II genes; MHC; diabetic nephropathy;
D O I
10.1016/S0198-8859(00)00174-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To analyze the contribution of MHC class II genes in type 2 diabetes mellitus (DM) with end stage renal disease (ESRD), we examined the distribution of HLA-DRB1, DQA1, DQB1 loci in Mexican Mestizos of General Mexico, using PCR-SSOP and PCR-SSP. Three groups were included: 47 type 2 diabetic ESRD patients; 42 patients with ESRD and 50 type 2 DM patients with no kidney complication. The results were compared with those of 101 controls of the same area. The median since DM was first diagnosed, was 18 years prior to the onset of ESRD, The frequencies of DRB1*1502 and DQB1*0501 were increased in DM patients with ESRD (p = 0.004; RR = 7.4, CI = 1.5-37; EF = 0.13; P = 0.007; RR = 2.9, CI = 2.3-3.5, EF = 0.21, respectively). In contrast, DRB1*0407 was decreased in the same group VI = 0.0008 RR = 0.2; CI = 0.035-0.70 PF = 0.19). Diabetic patients with DRB1*1502 are 8.8 times more likely to develop ESRD, independently of the duration time of DM. DRB1*1502 contributes to the susceptibility to ESRD while DRB1*0407 is involved in protect ion. The residue at DRB1-74 differs in these alleles: DRB1*0407 has glutamic acid and DRB1*1502 has an alanine, suggesting that this substitution may be important. for both, peptide anchoring and for presentation to the T cells. (C) American Society for Histocompatibility and Immunogenetics, 2000, Published by Elsevier Science Inc.
引用
收藏
页码:1031 / 1038
页数:8
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