Pascual Julio, Marcén Roberto, Zamora Javier, Fernández Ana M, Burgos Francisco J, Villafruela Juan J, Ortuño Joaquín
Nephrology Unit, Ramón y Cajal Hospital, Madrid, Spain.
J Nephrol. 2009 Jan-Feb;22(1):90-8.
Available studies of early serum creatinine (SCr) as a surrogate marker for long-term graft loss are multicenter, registry-based or limited to 5- to 7-year survival.
This was a single-center observational retrospective study. SCr during the first year post-kidney transplant as an independent variable in determining long-term (>10-year) graft survival in 754 first cadaver kidney transplants was assessed with univariate and multivariate models.
Kaplan-Meier survival estimates showed that recipient female sex, a transplant procedure performed after 1997, donor age under 55 years, immunosuppression including tacrolimus and/or mycophenolate mofetil and absence of acute rejection, were significantly related to better long-term graft survival. SCr at 1, 3, 6 and 12 months stratified into <or=1.5, 1.6-2 and >2 mg/dL groups was also strongly related to long-term graft survival. Multivariate Cox models showed that increased SCr at any point during the first year had a higher relative risk for ultimate graft loss.
Early graft function is strongly correlated with long-term graft survival (>or=10 years). Mild differences in SCr (1.5 vs. 1.6-2 mg/dL) are associated with highly significant impact on long-term survival, longer than previously described. However, the "hard" predictive value of SCr as an isolated tool is not strong enough. Other early surrogate end points for graft loss are needed.
现有关于早期血清肌酐(SCr)作为长期移植肾丢失替代标志物的研究多为多中心、基于登记处的研究,或仅限于5至7年的生存率。
这是一项单中心观察性回顾性研究。采用单变量和多变量模型评估了754例首次尸体肾移植中,肾移植术后第一年的SCr作为确定长期(>10年)移植肾存活的独立变量的情况。
Kaplan-Meier生存估计显示,受者为女性、1997年后进行的移植手术、供者年龄小于55岁、免疫抑制包括使用他克莫司和/或霉酚酸酯以及无急性排斥反应,均与更好的长期移植肾存活显著相关。将1、3、6和12个月时的SCr分层为≤1.5、1.6 - 2和>2mg/dL组,也与长期移植肾存活密切相关。多变量Cox模型显示,第一年中任何时间点SCr升高,最终移植肾丢失的相对风险更高。
早期移植肾功能与长期(≥10年)移植肾存活密切相关。SCr的轻微差异(1.5 vs. 1.6 - 2mg/dL)对长期存活有高度显著影响,且影响时间比先前描述的更长。然而,SCr作为单一工具的“硬”预测价值不够强。需要其他早期移植肾丢失的替代终点。