TY - JOUR
T1 - Evidence-based insomnia treatment strategy using novel orexin antagonists
T2 - A review
AU - Kishi, Taro
AU - Nishida, Maika
AU - Koebis, Michinori
AU - Taninaga, Takehiro
AU - Muramoto, Kenzo
AU - Kubota, Naoki
AU - Moline, Margaret
AU - Sakuma, Kenji
AU - Okuya, Makoto
AU - Nomura, Ikuo
AU - Iwata, Nakao
N1 - Publisher Copyright:
© 2021 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology
PY - 2021/12
Y1 - 2021/12
N2 - 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.
AB - 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.
KW - evidence-based medicine
KW - insomnia
KW - lemborexant
KW - network meta-analysis
KW - orexin
UR - https://www.scopus.com/pages/publications/85115295949
UR - https://www.scopus.com/inward/citedby.url?scp=85115295949&partnerID=8YFLogxK
U2 - 10.1002/npr2.12205
DO - 10.1002/npr2.12205
M3 - Review article
C2 - 34553844
AN - SCOPUS:85115295949
SN - 1340-2544
VL - 41
SP - 450
EP - 458
JO - Neuropsychopharmacology reports
JF - Neuropsychopharmacology reports
IS - 4
ER -