Influence of Interleukin-6 Promoter Polymorphism-174 G/C on Kidney Graft Outcome

被引:8
|
作者
Sanchez-Velasco, P. [2 ]
Rodrigo, E. [1 ]
Fernandez-Fresnedo, G. [1 ]
Ocejo-Vinyals, J. G. [2 ]
Ruiz, J. C. [1 ]
Arnau, A. [1 ]
Leyva-Cobian, F. [2 ]
Arias, M. [1 ,3 ,4 ]
机构
[1] Hosp Univ Marques de Valdecilla, Serv Nephrol, Santander 39008, Spain
[2] Hosp Univ Marques de Valdecilla, Serv Immunol, Santander 39008, Spain
[3] Univ Cantabria, Serv Cantabro Salud, E-39005 Santander, Spain
[4] Univ Cantabria, Dept Med & Psychiat, E-39005 Santander, Spain
关键词
TRANSPLANTATION; IL-6; HAPLOTYPES; IMPACT;
D O I
10.1016/j.transproceed.2010.07.041
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The cytokine interleukin-6 (IL-6) is important in both immune responses and cardiovascular diseases. The IL-6 promoter polymorphism -174 G/C is associated with increased plasma concentrations of IL-6. The relationship between IL-6 polymorphisms and graft survival, cardiovascular events, and new-onset diabetes mellitus after kidney transplantation is controversial. Objective. To analyze whether IL-6 (-174 G/C) polymorphism influences kidney graft survival or development of chronic allograft nephropathy, cardiovascular events, or new-onset diabetes. Methods. The IL-6 promoter polymorphism (-174 G/C) was analyzed using the polymerase chain reaction with sequence-specific primers in 335 kidney transplant recipients. Data for graft survival, chronic graft nephropathy, cardiovascular events, and new-onset diabetes were obtained retrospectively from clinical records. Categorical variables were compared between individuals with CC, GG, and GC genotypes using chi(2) tests. Survival analysis was performed using the Kaplan-Meier method, comparing groups using the log-rank test. Results. No significant differences were observed in 5-year graft survival between individuals with CC and GC/GG genotypes (85.3% vs 77.1%; P = .22). Nor were significant differences noted in the rates of chronic allograft nephropathy (37.5% vs 33.8%; P = .48), cardiovascular events (10.0% vs 23.0%; P = .10), or new-onset diabetes (7.5% vs 11.8%; P = .28). Conclusion. There is no association between IL-6 (-174 G/C) polymorphism and graft survival or development of chronic allograft nephropathy, cardiovascular events, or new-onset diabetes.
引用
收藏
页码:2854 / 2855
页数:2
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