Population Pharmacokinetics of Perampanel in Chinese Pediatric and Adult Patients With Epilepsy

吡仑帕奈 奥卡西平 卡马西平 癫痫 药代动力学 分配量 人口 医学 苯妥英钠 药理学 环境卫生 精神科
作者
Jiayu Yang,Sitian Zhang,Zhigang Zhao,Shenghui Mei,Weixing Feng
出处
期刊:Therapeutic Drug Monitoring [Lippincott Williams & Wilkins]
被引量:1
标识
DOI:10.1097/ftd.0000000000001296
摘要

Background: Perampanel is a promising epilepsy treatment with an innovative mechanism of action. This study was performed to investigate the factors affecting perampanel clearance in a population pharmacokinetic (PPK) model of Chinese pediatric and adult patients with epilepsy. Methods: A total of 135 perampanel plasma concentrations from 125 patients with epilepsy were analyzed using the PPK model with nonlinear mixed-effects modeling. One-compartment and proportional residual models best described the pharmacokinetics of perampanel. Covariate effects on the model parameters were assessed using forward and backward elimination. Goodness-of-fit, bootstrapping, visual predictive checks, and normalized prediction distribution errors were used to evaluate the model. Monte Carlo simulations were conducted to assess the impact of covariate combinations on perampanel plasma concentrations at different dosages. Results: In the final PPK model, body weight (BW), concomitant carbamazepine (CBZ), oxcarbazepine (OXC), and C-reactive protein (CRP) levels significantly influenced perampanel clearance. The interindividual clearance was calculated as follows: 0.84 × (BW/70) 0.53 × e CBZ × e OXC × e CRP (CBZ = 0.98, when comedicated with carbamazepine; OXC = 0.43, when comedicated with oxcarbazepine; CRP = −0.69, when CRP >15 mg/L, otherwise = 0). The estimates (relative standard error) for clearance and apparent volume of distribution of the final model were 0.84 L/h (8.75%) and 64.35 L (19.78%), respectively. The model maintained its stability and effectiveness with moderate predictability. Conclusions: BW and CBZ, OXC, and CRP levels may influence perampanel clearance in both pediatric and adult patients with epilepsy according to a population pharmacokinetic model that included real-world data.
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