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

机译:并用度洛西汀对利培酮和阿立哌唑稳态血药浓度的影响:一项基于治疗药物监测数据的研究。

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摘要

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.
机译:先前的研究已将度洛西汀归类为CYP2D6的中度抑制剂。本研究的目的是研究度洛西汀与两种CYP2D6底物利培酮和阿立哌唑之间在精神病患者中的潜在相互作用。利培酮(n = 8)或阿立哌唑(n = 7)与度洛西汀联用治疗的患者的血清浓度数据可从挪威奥斯陆Diakonhjemmet医院心理药理学中心的治疗药物监测档案中获取。通过将数据与使用口服利培酮或阿立哌唑但不使用度洛西汀的CYP2D6基因型对照组(纯合子“广泛代谢者”)进行比较,评估相互作用的程度。并用度洛西汀并没有显着增加母体药物的浓度或利培酮或阿立哌唑的母体药物/代谢物比率。因此,本研究表明度洛西汀可以安全地与利培酮或阿立哌唑同时使用。

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