Pharmacopsychiatry 2014; 47(03): 101-104
DOI: 10.1055/s-0034-1372644
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Effects of Escitalopram on Plasma Concentrations of Aripiprazole and its Active Metabolite, Dehydroaripiprazole, in Japanese Patients

Authors

  • K. Nemoto

    1   Department of Neuropsychiatry Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan
  • K. Mihara

    1   Department of Neuropsychiatry Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan
  • A. Nakamura

    1   Department of Neuropsychiatry Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan
  • G. Nagai

    1   Department of Neuropsychiatry Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan
  • S. Kagawa

    1   Department of Neuropsychiatry Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan
  • T. Suzuki

    1   Department of Neuropsychiatry Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan
    2   Department of Pharmacy Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan
  • T. Kondo

    1   Department of Neuropsychiatry Faculty of Medicine, University of the Ryukyus, Nishihara, Okinawa, Japan
Further Information

Publication History

received 06 February 2014
revised 20 March 2014

accepted 20 March 2014

Publication Date:
24 April 2014 (online)

Abstract

Introduction: 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.

Methods: 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.

Results: 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.

Conclusion: The present study suggests that low doses of escitalopram can be safely coadministered with aripiprazole, at least from a pharmacokinetic point of view.