Evidence‐based insomnia treatment strategy using novel orexin antagonists: A review

Abstract Most conventional insomnia medications are gamma‐aminobutylic acid receptor agonists. However, physical dependence is a concern and one of the major limiting factors for long‐term treatment. The dual orexin receptor antagonists, suvorexant and lemborexant, were recently approved for treatin...

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Main Authors: Taro Kishi, Maika Nishida, Michinori Koebis, Takehiro Taninaga, Kenzo Muramoto, Naoki Kubota, Margaret Moline, Kenji Sakuma, Makoto Okuya, Ikuo Nomura, Nakao Iwata
Format: Article
Language:English
Published: Wiley 2021-12-01
Series:Neuropsychopharmacology Reports
Subjects:
Online Access:https://doi.org/10.1002/npr2.12205
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author Taro Kishi
Maika Nishida
Michinori Koebis
Takehiro Taninaga
Kenzo Muramoto
Naoki Kubota
Margaret Moline
Kenji Sakuma
Makoto Okuya
Ikuo Nomura
Nakao Iwata
author_facet Taro Kishi
Maika Nishida
Michinori Koebis
Takehiro Taninaga
Kenzo Muramoto
Naoki Kubota
Margaret Moline
Kenji Sakuma
Makoto Okuya
Ikuo Nomura
Nakao Iwata
author_sort Taro Kishi
collection DOAJ
description Abstract Most conventional insomnia medications are gamma‐aminobutylic acid receptor agonists. However, physical dependence is a concern and one of the major limiting factors for long‐term treatment. The dual orexin receptor antagonists, suvorexant and lemborexant, were recently approved for treating chronic insomnia, giving a novel pharmacotherapeutic option. Because there are no comparative studies on these drugs, a network meta‐analysis was conducted, which is suitable for comparing interventions. According to this analysis, 5‐ and 10‐mg lemborexant were superior to 20‐mg suvorexant because of the greater improvement in initiating sleep after 1‐week administration. Furthermore, 5‐mg lemborexant (not 10 mg) and suvorexant were similarly well tolerated, without requiring discontinuation due to adverse events. We also overviewed the pharmacological and pharmacokinetic properties of lemborexant and suvorexant that may support these clinical outcomes. When compared to suvorexant, lemborexant quickly binds to the orexin receptors. The time to reach the maximum concentration after multiple administrations is shorter for lemborexant than for suvorexant. Considering these results, we recommend 5‐mg lemborexant as an initial treatment for insomnia, followed by 10‐mg lemborexant or suvorexant.
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spelling doaj.art-e1c3cd06cd9f45a8a585f4644d879cd02022-12-22T04:21:43ZengWileyNeuropsychopharmacology Reports2574-173X2021-12-0141445045810.1002/npr2.12205Evidence‐based insomnia treatment strategy using novel orexin antagonists: A reviewTaro Kishi0Maika Nishida1Michinori Koebis2Takehiro Taninaga3Kenzo Muramoto4Naoki Kubota5Margaret Moline6Kenji Sakuma7Makoto Okuya8Ikuo Nomura9Nakao Iwata10Department of Psychiatry Fujita Health University School of Medicine Toyoake Aichi JapanEisai Co., Ltd. Tokyo JapanEisai Co., Ltd. Tokyo JapanEisai Co., Ltd. Tokyo JapanEisai Co., Ltd. Tokyo JapanEisai Co., Ltd. Tokyo JapanEisai Inc. Woodcliff Lake New Jersey USADepartment of Psychiatry Fujita Health University School of Medicine Toyoake Aichi JapanDepartment of Psychiatry Fujita Health University School of Medicine Toyoake Aichi JapanDepartment of Psychiatry Fujita Health University School of Medicine Toyoake Aichi JapanDepartment of Psychiatry Fujita Health University School of Medicine Toyoake Aichi JapanAbstract Most conventional insomnia medications are gamma‐aminobutylic acid receptor agonists. However, physical dependence is a concern and one of the major limiting factors for long‐term treatment. The dual orexin receptor antagonists, suvorexant and lemborexant, were recently approved for treating chronic insomnia, giving a novel pharmacotherapeutic option. Because there are no comparative studies on these drugs, a network meta‐analysis was conducted, which is suitable for comparing interventions. According to this analysis, 5‐ and 10‐mg lemborexant were superior to 20‐mg suvorexant because of the greater improvement in initiating sleep after 1‐week administration. Furthermore, 5‐mg lemborexant (not 10 mg) and suvorexant were similarly well tolerated, without requiring discontinuation due to adverse events. We also overviewed the pharmacological and pharmacokinetic properties of lemborexant and suvorexant that may support these clinical outcomes. When compared to suvorexant, lemborexant quickly binds to the orexin receptors. The time to reach the maximum concentration after multiple administrations is shorter for lemborexant than for suvorexant. Considering these results, we recommend 5‐mg lemborexant as an initial treatment for insomnia, followed by 10‐mg lemborexant or suvorexant.https://doi.org/10.1002/npr2.12205evidence‐based medicineinsomnialemborexantnetwork meta‐analysisorexin
spellingShingle Taro Kishi
Maika Nishida
Michinori Koebis
Takehiro Taninaga
Kenzo Muramoto
Naoki Kubota
Margaret Moline
Kenji Sakuma
Makoto Okuya
Ikuo Nomura
Nakao Iwata
Evidence‐based insomnia treatment strategy using novel orexin antagonists: A review
Neuropsychopharmacology Reports
evidence‐based medicine
insomnia
lemborexant
network meta‐analysis
orexin
title Evidence‐based insomnia treatment strategy using novel orexin antagonists: A review
title_full Evidence‐based insomnia treatment strategy using novel orexin antagonists: A review
title_fullStr Evidence‐based insomnia treatment strategy using novel orexin antagonists: A review
title_full_unstemmed Evidence‐based insomnia treatment strategy using novel orexin antagonists: A review
title_short Evidence‐based insomnia treatment strategy using novel orexin antagonists: A review
title_sort evidence based insomnia treatment strategy using novel orexin antagonists a review
topic evidence‐based medicine
insomnia
lemborexant
network meta‐analysis
orexin
url https://doi.org/10.1002/npr2.12205
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