A pharmacokinetic analysis of amisulpride in adult Chinese patients with schizophrenia: Impact of creatinine clearance.

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY International journal of clinical pharmacology and therapeutics Pub Date : 2023-03-05 DOI:10.5414/CP204334
Wei Liu, Jingqi Zhou, Minjuan Cao, Fangming Zhang, Xiaoming Sun
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Abstract

Objective: To develop a stable population pharmacokinetic (PPK) model of amisulpride and to investigate the effects of covariates on the pharmacokinetic parameters in adult Chinese patients with schizophrenia.

Materials and methods: This retrospective study was carried out using 168 serum samples from 88 patients collected during routine clinical monitoring. Covariates recorded included demographic parameters (gender, age, weight), clinical parameters (serum creatinine, creatinine clearance), and intake of co-medications. The amisulpride PPK model was established using a nonlinear mixed effects modeling (NONMEM) approach. Goodness-of-fit (GOF) plots, bootstrap validation (1,000 runs), and normalized prediction distribution error (NPDE) were used in the evaluation of the final model.

Results: A one-compartment model with first-order absorption and elimination was developed. The population estimates for apparent clearance (CL/F) and apparent volume of distribution (V/F) were 32.6 L/h and 391 L, respectively. Estimated creatinine clearance (eCLcr) was a significant covariate for CL/F. The established model was: CL/F = 32.6 × (eCLcr/114.3)0.485 (L/h). The stability of the model was confirmed using GOF plots, bootstrap, and NPDE.

Conclusion: Creatinine clearance is a major covariate which is positively correlated with CL/F. Therefore, additional dose adjustments of amisulpride may be required on the basis of eCLcr. An ethnic difference may exist in the pharmacokinetics of amisulpride, but further research is needed in order to confirm this possibility. The PPK model of amisulpride for adult Chinese schizophrenic patients established here using NONMEM, is potentially an important tool for individualizing drug dosage and therapeutic drug monitoring.

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氨磺必利在中国成年精神分裂症患者中的药代动力学分析:肌酐清除率的影响。
摘要建立稳定的阿米舒必利群体药代动力学(PPK)模型,并研究共变量对中国成年精神分裂症患者药代动力学参数的影响:这项回顾性研究使用了在常规临床监测中收集的 88 名患者的 168 份血清样本。记录的协变量包括人口统计学参数(性别、年龄、体重)、临床参数(血清肌酐、肌酐清除率)和联合用药情况。采用非线性混合效应建模(NONMEM)方法建立了阿米舒必利 PPK 模型。在评估最终模型时使用了拟合优度(GOF)图、引导验证(1,000 次运行)和归一化预测分布误差(NPDE):结果:建立了一个具有一阶吸收和消除的单室模型。表观清除率(CL/F)和表观分布容积(V/F)的人群估计值分别为 32.6 升/小时和 391 升。估计肌酐清除率(eCLcr)是 CL/F 的重要协变量。建立的模型为CL/F = 32.6 × (eCLcr/114.3)0.485 (L/h)。该模型的稳定性通过 GOF 图、bootstrap 和 NPDE 得到证实:结论:肌酐清除率是与 CL/F 呈正相关的主要协变量。因此,可能需要根据 eCLcr 调整阿米舒必利的剂量。氨磺必利的药代动力学可能存在种族差异,但需要进一步研究才能证实这种可能性。本文利用NONMEM建立的中国成年精神分裂症患者氨磺必利的PPK模型可能是个体化用药和治疗药物监测的重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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