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他克莫司变异系数评分优于变异系数,可预测活体肾移植的临床结局。

Tacrolimus variability score outperforms coefficient of variation in predicting clinical outcomes of living kidney transplantation.

机构信息

Urology Department/Urology research institute/Organ transplantation center, West China Hospital, Sichuan University, Chengdu City, Sichuan Province, China.

West China Medical School, Sichuan University, Chengdu City, Sichuan Province, China.

出版信息

Br J Clin Pharmacol. 2022 Jan;88(1):75-83. doi: 10.1111/bcp.14876. Epub 2021 May 12.

Abstract

AIMS

Intrapatient variability (IPV) was previously defined as coefficient of variation (CV) or standard deviation of tacrolimus (Tac) exposure while none of them was easily being interpreted and translated into clinical practice after kidney transplantation.

METHODS

We developed a novel Tac variability score (TVS) to evaluate IPV by calculating the frequency of clinically significant changes of Tac trough levels after kidney transplantation. Multivariate Cox proportional analyses were conducted to compare the impact of TVS and CV on transplant outcomes.

RESULTS

A total of 1343 patients were divided into high TVS (>0.30) and low TVS (<0.30) groups, and low CV (<0.30) and high CV (>0.30) groups. Univariate analyses showed that high TVS (hazard ratio [HR]: 2.323, 95% confidence interval [CI]: 1.455-3.709) and high CV (HR: 1.606, 95%CI: 1.044-2.471) were associated with inferior graft survival. However, only TVS was an independent predictor for graft failure in multivariate analyses (HR: 1.972, 95%CI: 1.2-3.24), and the correlation maintained in high CV (P = .020) and low CV (P = .037) subgroups, while CV failed to predict graft loss in neither low (P = .387) nor high TVS (P = .600) subgroups. In addition, TVS had a higher correlation with graft survival in patients with Tac exposure within the therapeutic range and the correlation was less influenced by mean Tac trough levels.

CONCLUSION

TVS is a novel measure of Tac IPV with higher correlation with graft survival and more convenience in clinical use than CV after kidney transplantation.

摘要

目的

先前,个体内变异(IPV)被定义为环孢素(Tac)暴露的变异系数(CV)或标准差,但在肾移植后,它们均不易解释且难以转化为临床实践。

方法

我们开发了一种新的 Tac 变异评分(TVS),通过计算肾移植后 Tac 谷浓度的临床显著变化频率来评估 IPV。采用多变量 Cox 比例风险分析比较 TVS 和 CV 对移植结局的影响。

结果

共纳入 1343 例患者,分为 TVS 较高(>0.30)和较低(<0.30)组,以及 CV 较高(>0.30)和较低(<0.30)组。单因素分析显示,TVS 较高(风险比 [HR]:2.323,95%置信区间 [CI]:1.455-3.709)和 CV 较高(HR:1.606,95%CI:1.044-2.471)与移植物存活率降低相关。然而,仅 TVS 在多因素分析中是移植物失功的独立预测因子(HR:1.972,95%CI:1.2-3.24),且在 CV 较高(P = .020)和较低(P = .037)亚组中相关性保持,而 CV 在低 TVS(P = .387)和高 TVS(P = .600)亚组中均未能预测移植物丢失。此外,在 Tac 暴露于治疗范围内的患者中,TVS 与移植物存活率的相关性更高,且与 Tac 谷浓度的相关性受影响更小。

结论

TVS 是 Tac IPV 的一种新的衡量指标,与肾移植后移植物存活率的相关性更高,且比 CV 更方便临床应用。

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