Nemoto K, Mihara K, Nakamura A, Nagai G, Kagawa S, Suzuki T, Kondo T
Department of Neuropsychiatry Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan.
Pharmacopsychiatry. 2014 May;47(3):101-4. doi: 10.1055/s-0034-1372644. Epub 2014 Apr 24.
The effects of escitalopram (10 mg/d) coadministration on plasma concentrations of aripiprazole and its active metabolite, dehydroaripiprazole, were studied in 13 Japanese psychiatric patients and compared with those of paroxetine (10 mg/d) coadministration.
The patients had received 6-24 mg/d of aripiprazole for at least 2 weeks. Patients were randomly allocated to one of 2 treatment sequences: paroxetine-escitalopram (n=6) or escitalopram-paroxetine (n=7). Each sequence consisted of two 2-week phases. Plasma concentrations of aripiprazole and dehydroaripiprazole were measured using liquid chromatography with mass spectrometric detection.
Plasma concentrations of aripiprazole and the sum of aripiprazole and dehydroaripiprazole during paroxetine coadministration were 1.7-fold (95% confidence intervals [CI], 1.3-2.1, p<0.001) and 1.5-fold (95% CI 1.2-1.9, p<0.01) higher than those values before the coadministration. These values were not influenced by escitalopram coadministration (1.3-fold, 95% CI 1.1-1.5 and 1.3-fold, 95% CI 1.0-1.5). Plasma dehydroaripiprazole concentrations remained constant during the study.
The present study suggests that low doses of escitalopram can be safely coadministered with aripiprazole, at least from a pharmacokinetic point of view.
在13名日本精神病患者中研究了艾司西酞普兰(10毫克/天)联合用药对阿立哌唑及其活性代谢物去氢阿立哌唑血浆浓度的影响,并与帕罗西汀(10毫克/天)联合用药的情况进行了比较。
患者接受6 - 24毫克/天的阿立哌唑治疗至少2周。患者被随机分配到2种治疗顺序之一:帕罗西汀 - 艾司西酞普兰组(n = 6)或艾司西酞普兰 - 帕罗西汀组(n = 7)。每个顺序包括两个2周阶段。使用液相色谱 - 质谱检测法测量阿立哌唑和去氢阿立哌唑的血浆浓度。
帕罗西汀联合用药期间阿立哌唑的血浆浓度以及阿立哌唑和去氢阿立哌唑的血浆浓度总和分别比联合用药前高1.7倍(95%置信区间[CI],1.3 - 2.1,p < 0.001)和1.5倍(95% CI 1.2 - 1.9,p < 0.01)。这些值不受艾司西酞普兰联合用药的影响(分别为1.3倍,95% CI 1.1 - 1.5和1.3倍,95% CI 1.0 - 1.5)。在研究期间血浆去氢阿立哌唑浓度保持恒定。
本研究表明,至少从药代动力学角度来看,低剂量的艾司西酞普兰可与阿立哌唑安全地联合使用。