Evidence map›Paper›PMID 42717137›Full record

ArticleJournal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine2026

Dual orexin receptor antagonist-assisted dose reduction of benzodiazepines and benzodiazepine receptor agonists: a mirror-image analysis of insurance claims data.

Kentaro Matsui, Ko Sugiura, Akiyoshi Shimura, Shunsuke Takagi, Kazuhiro Kurihara, Yoshikazu Takaesu, Yuichi Inoue

Abstract read
In one paragraph

Article in Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Deprescribing benzodiazepine hypnotics and Z-drugs: are DORAs the answer?Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Kentaro MatsuiDepartment of Sleep Medicine, National Center of Neurology and Psychiatry, National Center Hospital, Tokyo, Japan.
Ko SugiuraDepartment of Economics, Ghent University, Ghent, Belgium.
Akiyoshi ShimuraJapan Somnology Center, Neuropsychiatric Research Institute, Tokyo, Japan.
Shunsuke TakagiDepartment of Psychiatry and Behavioral Science, Institute of Science Tokyo, Tokyo, Japan.
Kazuhiro KuriharaDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Yoshikazu TakaesuDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Yuichi InoueJapan Somnology Center, Neuropsychiatric Research Institute, Tokyo, Japan. inoue@somnology.com.ORCID http://orcid.org/0000-0001-7414-9017

Funding

Japan Society for the Promotion of Science 22K15778
6 · The paper itself

Abstract

purposeDiscontinuing benzodiazepines and benzodiazepine receptor agonists (BZ/BZRAs) remains challenging for patients with chronic insomnia despite safety concerns. This study evaluated whether continuous treatment with dual orexin receptor antagonists (DORAs) facilitates a reduction in BZ/BZRA doses among long-term users.

methodsThis self-controlled (mirror-image) study, in which each patient served as their own control, used Japanese health insurance claims data (Dokenpo database, 2019-2024). Eligible patients had continuous BZ/BZRA use for ≥ 6 months and initiated suvorexant or lemborexant for ≥ 6 months. Changes in bedtime BZ/BZRA dose (diazepam equivalents) were compared between pre- and post-DORA periods. Logistic regression analyses identified factors associated with ≥ 50% dose reduction and BZ/BZRA discontinuation.

resultsPrior to DORA initiation, 605 patients were taking a mean of 1.9 ± 1.0 types of BZ/BZRAs at a pretreatment total daily dose of 8.2 ± 7.4 mg diazepam equivalent. Of these, 42.1% achieved ≥ 50% bedtime BZ/BZRA dose reduction and 21.3% achieved discontinuation. Mean bedtime doses decreased in both the suvorexant group (7.2 to 5.2 mg) and the lemborexant group (8.3 to 5.2 mg). In adjusted analyses, age ≥ 65 years was independently associated with both ≥ 50% reduction (odds ratio [OR] 2.485; 95% confidence interval [CI] 1.190-5.192; p = 0.015) and discontinuation (OR 2.636; 95% CI 1.158-6.000; p = 0.021). Lower pretreatment BZ/BZRA dose and lemborexant use were also associated with dose reduction and discontinuation.

conclusionDORA treatment for at least six months may support BZ/BZRA dose reduction among long-term users, particularly in older patients. CURRENT KNOWLEDGE/STUDY RATIONALE: Discontinuing benzodiazepine and benzodiazepine receptor agonists (BZ/BZRAs) in patients with long-term use remains clinically challenging despite well-documented safety concerns. Whether sustained treatment with dual orexin receptor antagonists (DORAs) facilitates BZ/BZRA dose reduction in real-world practice has not been adequately examined in patients already exposed for six months or longer. STUDY IMPACT: Sustained DORA treatment for at least six months was associated with substantial bedtime BZ/BZRA dose reduction and discontinuation among long-term users, with older adults (aged 65 years or older) showing the highest odds of success. These findings support DORA co-administration as a practical pharmacological switching strategy to enable safer insomnia management, particularly in populations vulnerable to BZ/BZRA-related adverse events.

Indexed as

BenzodiazepinesGABA-A Receptor AgonistsOrexin Receptor AntagonistsSleep Initiation and Maintenance DisordersAdultAgedAzepinesDose-Response Relationship, DrugFemaleHumansInsurance Claim ReviewJapanMaleMiddle AgedPyridinesPyrimidinesAzepinesBenzodiazepinesGABA-A Receptor AgonistslemborexantOrexin Receptor AntagonistsPyridinesPyrimidinessuvorexantTriazolesBenzodiazepinesDeprescriptionsHypnotics and sedativesInsomniaOrexin receptor antagonists

Identifiers

PMID42717137
PMCPMC13558528

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.