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基于群体药代动力学的精神分裂症患者阿立哌唑的药物相互作用及初始剂量优化

Drug-drug interaction and initial dosage optimization of aripiprazole in patients with schizophrenia based on population pharmacokinetics.

作者信息

Zhang Cun, Jiang Lei, Hu Ke, Zhang Yi-Jia, Han Jing, Chen Jin, Dong Boling, Shi Hao-Zhe, He Su-Mei, Yu Ting-Ting, Chen Xiao, Wang Dong-Dong

机构信息

Department of Pharmacy, Xuzhou Oriental Hospital Affiliated to Xuzhou Medical University, Xuzhou, Jiangsu, China.

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy and School of Pharmacy, Xuzhou Medical University, Xuzhou, Jiangsu, China.

出版信息

Front Psychiatry. 2024 Jun 18;15:1377268. doi: 10.3389/fpsyt.2024.1377268. eCollection 2024.

Abstract

BACKGROUND

The present study aimed to investigate the drug-drug interaction and initial dosage optimization of aripiprazole in patients with schizophrenia based on population pharmacokinetics.

RESEARCH DESIGN AND METHODS

A total of 119 patients with schizophrenia treated with aripiprazole were included to build an aripiprazole population pharmacokinetic model using nonlinear mixed effects.

RESULTS

The weight and concomitant medication of fluoxetine influenced aripiprazole clearance. Under the same weight, the aripiprazole clearance rates were 0.714:1 in patients with or without fluoxetine, respectively. In addition, without fluoxetine, for the once-daily aripiprazole regimen, dosages of 0.3 and 0.2 mg kg day were recommended for patients with schizophrenia weighing 40-95 and 95-120 kg, respectively, while for the twice-daily aripiprazole regimen, 0.3 mg kg day was recommended for those weighing 40-120 kg. With fluoxetine, for the once-daily aripiprazole regimen, a dosage of 0.2 mg kg day was recommended for patients with schizophrenia weighing 40-120 kg, while for the twice-daily aripiprazole regimen, 0.3 and 0.2 mg kg day were recommended for those weighing 40-60 and 60-120 kg, respectively.

CONCLUSION

This is the first investigation of the effects of fluoxetine on aripiprazole via drug-drug interaction. The optimal aripiprazole initial dosage is recommended in patients with schizophrenia.

摘要

背景

本研究旨在基于群体药代动力学研究阿立哌唑在精神分裂症患者中的药物相互作用及初始剂量优化。

研究设计与方法

纳入119例接受阿立哌唑治疗的精神分裂症患者,采用非线性混合效应建立阿立哌唑群体药代动力学模型。

结果

体重及氟西汀的合并用药影响阿立哌唑清除率。在相同体重下,服用或未服用氟西汀患者的阿立哌唑清除率分别为0.714:1。此外,未服用氟西汀时,对于阿立哌唑每日一次给药方案,体重40 - 95 kg和95 - 120 kg的精神分裂症患者推荐剂量分别为0.3和0.2 mg·kg·d,而对于阿立哌唑每日两次给药方案,体重40 - 120 kg的患者推荐剂量为0.3 mg·kg·d。服用氟西汀时,对于阿立哌唑每日一次给药方案,体重40 - 120 kg的精神分裂症患者推荐剂量为0.2 mg·kg·d,而对于阿立哌唑每日两次给药方案,体重40 - 60 kg和60 - 120 kg的患者推荐剂量分别为0.3和0.2 mg·kg·d。

结论

这是首次通过药物相互作用研究氟西汀对阿立哌唑的影响。为精神分裂症患者推荐了阿立哌唑的最佳初始剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/636e/11217561/3845d60ffdbd/fpsyt-15-1377268-g001.jpg

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