Ito Satoko, Yano Ikuko, Hashi Sachiyo, Tsuda Masahiro, Sugimoto Mitsuhiro, Yonezawa Atsushi, Ikeda Akio, Matsubara Kazuo
*Department of Clinical Pharmacy and Education, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan; †Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital, Kyoto, Japan; and ‡Department of Epilepsy, Movement Disorders and Physiology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Ther Drug Monit. 2016 Jun;38(3):371-8. doi: 10.1097/FTD.0000000000000291.
Levetiracetam, a second-generation antiepileptic drug, is frequently used for managing partial-onset seizures. About 70% of the administered dose is excreted in urine unchanged, and dosage adjustment is recommended based on the individual's renal function. In this study, a population pharmacokinetic model of levetiracetam was developed using routinely monitored serum concentration data for individualized levetiracetam therapy.
Patients whose serum concentrations of levetiracetam at steady-state were routinely monitored at Kyoto University Hospital from April 2012 to March 2013 were enrolled. The influence of patient characteristics on levetiracetam pharmacokinetics was evaluated using the nonlinear mixed-effects modeling (NONMEM) program.
A total of 583 steady-state concentrations from 225 patients were used for the analysis. The median patient age and estimated glomerular filtration rate (eGFR) were 38 (range: 1-89) years and 98 (15-189) mL·min·1.73 m, respectively. Serum concentration-time data of levetiracetam were well described by a 1-compartment model with first-order absorption. Oral clearance was allometrically related to the individual body weight and eGFR. An increase in the dose significantly increased oral clearance. No improvement in model fit was observed by including the covariate of any concomitant antiepileptic drugs. The population mean clearance for an adult weighing 70 kg and with a normal renal function was 4.8 and 5.9 L/h for 500 mg bis in die (bid) and 1500 mg bid, respectively.
Oral clearance allometrically related with body weight and eGFR can well predict the routine therapeutic drug monitoring data from pediatric to aged patients with varying renal function. Dosage adjustments based on renal function are effective in controlling the trough and peak concentrations in similar ranges.
左乙拉西坦是一种第二代抗癫痫药物,常用于治疗部分性发作。约70%的给药剂量以原形经尿液排泄,建议根据个体肾功能调整剂量。在本研究中,利用左乙拉西坦治疗期间常规监测的血清浓度数据,建立了左乙拉西坦的群体药代动力学模型,用于个体化治疗。
纳入2012年4月至2013年3月在京都大学医院常规监测左乙拉西坦稳态血清浓度的患者。采用非线性混合效应模型(NONMEM)程序评估患者特征对左乙拉西坦药代动力学的影响。
共分析了225例患者的583个稳态浓度。患者年龄中位数和估计肾小球滤过率(eGFR)分别为38(范围:1 - 89)岁和98(15 - 189)mL·min·1.73 m²。左乙拉西坦的血清浓度 - 时间数据用具有一级吸收的单室模型能很好地描述。口服清除率与个体体重和eGFR呈异速生长关系。剂量增加显著提高口服清除率。纳入任何联合使用的抗癫痫药物的协变量后,模型拟合未得到改善。体重70 kg且肾功能正常的成年人,500 mg每日两次(bid)和1500 mg bid时的群体平均清除率分别为4.8和5.9 L/h。
与体重和eGFR呈异速生长关系的口服清除率能够很好地预测不同肾功能的儿童至老年患者的常规治疗药物监测数据。根据肾功能调整剂量可有效将谷浓度和峰浓度控制在相似范围内。