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度洛西汀对利培酮和阿立哌唑稳态血清浓度的影响:基于治疗药物监测数据的研究。

The effect of coadministration of duloxetine on steady-state serum concentration of risperidone and aripiprazole: a study based on therapeutic drug monitoring data.

机构信息

Center for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.

出版信息

Ther Drug Monit. 2010 Dec;32(6):787-90. doi: 10.1097/FTD.0b013e3181fc50d5.

DOI:10.1097/FTD.0b013e3181fc50d5
PMID:21068650
Abstract

Previous studies have categorized duloxetine as a moderate inhibitor of CYP2D6. The aim of the present study was to investigate the potential interactions between duloxetine and the two CYP2D6 substrates risperidone and aripiprazole in psychiatric patients. Serum concentration data from patients treated with risperidone (n = 8) or aripiprazole (n = 7) in combination with duloxetine were retrieved from therapeutic drug monitoring files at the Center for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway. The degree of interaction was assessed by comparing the data with a control group of CYP2D6-genotyped patients (homozygous "extensive metabolizers") using oral risperidone or aripiprazole without duloxetine. Coadministration of duloxetine did not significantly increase the concentration of the parent drug or the parent drug/metabolite ratio of either risperidone or aripiprazole. The present study therefore indicates that duloxetine may safely be used concomitantly with risperidone or aripiprazole.

摘要

先前的研究将度洛西汀归类为 CYP2D6 的中度抑制剂。本研究旨在调查度洛西汀与两种 CYP2D6 底物利培酮和阿立哌唑在精神科患者中的潜在相互作用。从挪威奥斯陆 Diakonhjemmet 医院精神药理学中心的治疗药物监测文件中检索到同时接受度洛西汀治疗的利培酮(n = 8)或阿立哌唑(n = 7)患者的血清浓度数据。通过与 CYP2D6 基因分型患者(纯合“广泛代谢者”)的对照组(口服利培酮或阿立哌唑而不使用度洛西汀)比较数据,评估相互作用的程度。度洛西汀的共同给药并未显著增加利培酮或阿立哌唑的母体药物或母体药物/代谢物比值的浓度。因此,本研究表明度洛西汀可与利培酮或阿立哌唑同时安全使用。

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