Department of Nephrology, University of Queensland at the Princess Alexandra Hospital, Brisbane, Qld, Australia.
Transpl Int. 2012 Nov;25(11):1182-93. doi: 10.1111/j.1432-2277.2012.01553.x. Epub 2012 Sep 5.
This study analysed associations between tacrolimus, mycophenolic acid (MPA) and prednisolone exposures on day 4 and month 1 post kidney transplant and clinical outcomes. Area under the concentration-time curve (AUC) for each drug was estimated using validated multiple regression-derived limited sampling strategies. Multivariate logistic regression was used to associate drug exposure with clinical outcomes. One hundred and twenty subjects were studied. Between-subject variability in dose-adjusted exposure to each medication was high. Both day 4 tacrolimus and MPA exposures were independently predictive of delayed graft function (2.6 change in odds for a standard deviation (SD) increase in tacrolimus AUC(0-12) , P = 0.02; 0.23 change in odds for a SD increase in MPA AUC(0-12) , P = 0.02). Both day 4 MPA and total prednisolone exposures were independently predictive of rejection (0.20 change in odds for a SD increase in MPA AUC(0-12) , P = 0.04; 0.40 change in odds for a SD increase in total prednisolone AUC(0-6) , P = 0.03). Lowest tertile exposure to all three immunosuppressant medications imposed significantly higher odds of rejection [adjusted odds ratio 34.2 (95% CI 4.1, 284.4), P = 0.001]. This study highlights the importance of achieving early target exposure and suggests a potential role for individualized initial dosing or early therapeutic monitoring of all three immunosuppressive agents.
本研究分析了肾移植后第 4 天和第 1 个月他克莫司、霉酚酸(MPA)和泼尼松龙暴露与临床结果之间的关系。使用验证的多回归衍生有限采样策略估计每种药物的浓度-时间曲线下面积(AUC)。多变量逻辑回归用于将药物暴露与临床结果相关联。对 120 名受试者进行了研究。每种药物的剂量调整暴露的个体间变异性很高。第 4 天他克莫司和 MPA 的暴露均独立预测延迟移植物功能(他克莫司 AUC(0-12)的标准偏差(SD)增加一个单位,比值比变化 2.6,P=0.02;MPA AUC(0-12)的 SD 增加一个单位,比值比变化 0.23,P=0.02)。第 4 天 MPA 和总泼尼松龙的暴露均独立预测排斥反应(MPA AUC(0-12)的 SD 增加一个单位,比值比变化 0.20,P=0.04;总泼尼松龙 AUC(0-6)的 SD 增加一个单位,比值比变化 0.40,P=0.03)。三种免疫抑制剂药物的最低三分位暴露显著增加了排斥反应的可能性[调整比值比 34.2(95%CI 4.1,284.4),P=0.001]。本研究强调了达到早期目标暴露的重要性,并提示了对所有三种免疫抑制剂进行个体化初始剂量或早期治疗监测的潜在作用。