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Influence of tacrolimus metabolism rate on renal function after solid organ transplantation

机译:他克莫司代谢率对实体器官移植后肾功能的影响

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摘要

The calcineurin inhibitor (CNI) tacrolimus (TAC) is an integral part of the immunosuppressive regimen after solid organ transplantation. Although TAC is very effective in prevention of acute rejection episodes, its highly variable pharmacokinetic and narrow therapeutic window require frequent monitoring of drug levels and dose adjustments. TAC can cause CNI nephrotoxicity even at low blood trough levels (4-6 ng/mL). Thus, other factors besides the TAC trough level might contribute to CNI-related kidney injury. Unfortunately, TAC pharmacokinetic is determined by a whole bunch of parameters. However, for daily clinical routine a simple application strategy is needed. To address this problem, we and others have evaluated a simple calculation method in which the TAC blood trough concentration (C) is divided by the daily dose (D). Fast TAC metabolism (C/D ratio < 1.05) was identified as a potential risk factor for an inferior kidney function after transplantation. In this regard, we recently showed a strong association between fast TAC metabolism and CNI nephrotoxicity as well as BKV infection. Therefore, the TAC C/D ratio may assist transplant clinicians in a simple way to individualize the immunosuppressive regimen.
机译:钙调神经磷酸酶抑制剂(CNI)他克莫司(TAC)是实体器官移植后免疫抑制方案不可或缺的一部分。尽管TAC在预防急性排斥反应方面非常有效,但其高度可变的药代动力学和狭窄的治疗范围要求经常监测药物水平和剂量调整。 TAC甚至可以在低血谷水平(4-6 ng / mL)时引起CNI肾毒性。因此,除了TAC低谷水平外,其他因素也可能导致CNI相关的肾脏损伤。不幸的是,TAC的药代动力学由许多参数决定。但是,对于日常临床常规,需要一种简单的应用策略。为了解决这个问题,我们和其他人评估了一种简单的计算方法,其中TAC血谷浓度(C)除以日剂量(D)。 TAC快速代谢(C / D比<1.05)被确定为移植后肾功能低下的潜在危险因素。在这方面,我们最近显示出快速的TAC代谢和CNI肾毒性以及BKV感染之间有很强的联系。因此,TAC C / D比可以以简单的方式帮助移植临床医生个体化免疫抑制方案。

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