Influence of interleukin-6 promoter polymorphism -174 g/c on kidney graft outcome |
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Authors: | Sánchez-Velasco P Rodrigo E Fernández-Fresnedo G Ocejo-Vinyals J G Ruiz J C Arnau A Leyva-Cobián F Arias M |
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Affiliation: | a Service of Immunology, Hospital Universitario Marqués de Valdecilla, Servicio Cántabro de Salud, Santander, Spain b Service of Nephrology, Hospital Universitario Marqués de Valdecilla, Servicio Cántabro de Salud, Santander, Spain c Department of Medicine and Psychiatry, University of Cantabria, Santander, Spain |
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Abstract: | BackgroundThe 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.ObjectiveTo analyze whether IL-6 (−174 G/C) polymorphism influences kidney graft survival or development of chronic allograft nephropathy, cardiovascular events, or new- onset diabetes.MethodsThe 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 χ2 tests. Survival analysis was performed using the Kaplan-Meier method, comparing groups using the log-rank test.ResultsNo 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).ConclusionThere 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. |
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