1] Division of Nephrology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada [2] Division of Nephrology and the Kidney Transplant Program, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
Division of Nephrology and the Kidney Transplant Program, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
Kidney Int. 2014 Jun;85(6):1404-11. doi: 10.1038/ki.2013.465. Epub 2013 Dec 11.
Wide variations in tacrolimus levels have been identified as a risk factor for inferior kidney allograft survival but past studies have not properly accounted for the dynamic nature of drug exposure over time. Here we evaluated whether time-varying exposure to tacrolimus increases the risk of long-term adverse outcomes in a retrospective cohort study in adult kidney transplant recipients on tacrolimus-based immunosuppression. Time-dependent Cox proportional hazards models were used to examine the association between the standard deviation of tacrolimus levels (TacSD) starting at 1-year post-transplant and the composite end point of late allograft rejection, transplant glomerulopathy, or total graft loss (including death). Among 356 patients, there was a significant 27% increase in the adjusted hazard of the composite end point for every 1-unit increase in TacSD (hazard ratio 1.27 (95% confidence interval 1.03, 1.56)). There was also a graded increase in the relative hazard for the composite end point by TacSD threshold (hazard ratios 1.33, 1.50, 1.84, and 2.56 for TacSD 1.5, 2, 2.5, and 3, respectively). The results were similar for total graft loss and the composite end point excluding death. Thus, increased time-dependent TacSD may be an independent risk factor for adverse kidney transplant outcomes. TacSD may serve as a monitoring tool to identify high-risk patients. Whether interventions to decrease TacSD will improve outcomes requires further study.
环孢素水平的广泛变化已被确定为肾移植后移植物存活率降低的一个风险因素,但过去的研究并没有正确考虑药物暴露随时间的动态变化。在这里,我们在接受基于环孢素的免疫抑制治疗的成年肾移植受者的回顾性队列研究中评估了环孢素的时变暴露是否会增加长期不良结局的风险。使用时依 Cox 比例风险模型来检查移植后 1 年开始时环孢素水平(TacSD)的标准差与晚期移植物排斥、移植肾小球病或总移植物丢失(包括死亡)的复合终点之间的关联。在 356 名患者中,TacSD 每增加 1 个单位,复合终点的调整后危险比增加 27%(危险比 1.27(95%置信区间 1.03, 1.56))。复合终点的相对危险也随 TacSD 阈值呈梯度增加(TacSD 分别为 1.5、2、2.5 和 3 时,危险比为 1.33、1.50、1.84 和 2.56)。TacSD 与总移植物丢失和排除死亡的复合终点的结果相似。因此,增加的时间依赖性 TacSD 可能是不良肾移植结局的独立危险因素。TacSD 可作为一种监测工具,以识别高危患者。是否干预降低 TacSD 将改善结局需要进一步研究。