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Explaining variability in tacrolimus pharmacokinetics to optimize early exposure in adult kidney transplant recipients.

机译:解释他克莫司药代动力学的变异性,以优化成年肾移植受者的早期暴露。

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To prevent acute rejection episodes, it is important to reach adequate tacrolimus (TRL) exposure early after kidney transplantation. With a better understanding of the high variability in the pharmacokinetics of TRL, the starting dose can be individualized, resulting in a reduction in dose adjustments to obtain the target exposure. A population pharmacokinetic analysis was performed to estimate the effects of demographic factors, hematocrit, serum albumin concentration, prednisolone dose, TRL dose interval, polymorphisms in genes coding for ABCB1, CYP3A5, CYP3A4, and the pregnane X receptor on TRL pharmacokinetics. Pharmacokinetic data were prospectively obtained in 31 de novo kidney transplant patients randomized to receive TRL once or twice daily, and subsequently, the data were analyzed by means of nonlinear mixed-effects modeling. TRL clearance was 1.5-fold higher for patients with the CYP3A5*1/*3 genotype compared with the CYP3A5*3/*3 genotype (5.5 +/- 0.5 L/h versus 3.7 +/- 0.3 L/h, respectively). This factor explained 30% of the interindividual variability in apparent clearance (exposure). Also, a relationship between the pregnane X receptor A+7635G genotype and TRL clearance was identified with a clearance of 3.9 +/- 0.3 L/h in the A allele carriers versus 5.4 +/- 0.6 L/h in the GG genotype. Finally, a concomitant prednisolone dose of more than 10 mg/d increased the TRL apparent clearance by 15%. In contrast, body weight was not related to TRL clearance in this population. Because patients are typically dosed per kilogram body weight, this might result in underexposure and overexposure in patients, with a low and high body weight, respectively. This integrated analysis shows that adult renal transplant recipients with the CYP3A5*1/*3 genotype require a 1.5 times higher, fixed, starting dose compared with CYP3A5*3/*3 to reach the predefined target exposure early after transplantation.
机译:为防止急性排斥反应发作,重要的是在肾脏移植后尽早达到足够的他克莫司(TRL)暴露。更好地了解TRL药代动力学的高变异性后,就可以对起始剂量进行个体化,从而减少剂量调整以获得目标暴露量。进行了群体药代动力学分析,以评估人口统计学因素,血细胞比容,血清白蛋白浓度,泼尼松龙剂量,TRL剂量间隔,编码ABCB1,CYP3A5,CYP3A4的基因多态性以及妊娠X受体对TRL药代动力学的影响。前瞻性地从31名每天接受一次或两次TRL的新肾移植患者中获得药代动力学数据,然后通过非线性混合效应模型对数据进行分析。与CYP3A5 * 3 / * 3基因型相比,CYP3A5 * 1 / * 3基因型患者的TRL清除率高1.5倍(分别为5.5 +/- 0.5 L / h和3.7 +/- 0.3 L / h)。该因素解释了表观清除率(暴露)中个体间差异的30%。而且,确定了孕烷X受体A + 7635G基因型与TRL清除之间的关系,在A等位基因携带者中的清除率为3.9 +/- 0.3 L / h,而在GG基因型中为5.4 +/- 0.6 L / h。最后,同时强的松龙剂量大于10 mg / d可使TRL表观清除率增加15%。相反,该人群的体重与TRL清除率无关。因为患者通常按每千克体重服用,这可能会导致低体重和高体重的患者暴露不足和过度暴露。这项综合分析表明,具有CYP3A5 * 1 / * 3基因型的成年肾移植受者需要比CYP3A5 * 3 / * 3高1.5倍的固定起始剂量,才能在移植后早期达到预定的目标暴露水平。

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