Evidence map›Paper›PMID 42052562›Full record

ArticleSleep advances : a journal of the Sleep Research Society2026

Effects of lemborexant and zolpidem on sleep electroencephalography in older adults with insomnia: a randomized trial.

Negin Sattari, Abhishek Dave, Hamid Niknazar, Ivy Y Chen, Ariel B Neikrug, Bryce A Mander, Ruth M Benca

Abstract read
In one paragraph

Article in Sleep advances : a journal of the Sleep Research Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Negin SattariDepartment of Psychiatry and Human Behavior, University of California Irvine, Irvine, CA, United States.
Abhishek DaveDepartment of Psychiatry and Human Behavior, University of California Irvine, Irvine, CA, United States.ORCID https://orcid.org/0000-0002-6186-027X
Hamid NiknazarDepartment of Cognitive Sciences, University of California, Irvine, Irvine, CA, United States.
Ivy Y ChenDepartment of Psychiatry and Human Behavior, University of California Irvine, Irvine, CA, United States.ORCID https://orcid.org/0000-0002-6739-3211
Ariel B NeikrugDepartment of Psychiatry and Human Behavior, University of California Irvine, Irvine, CA, United States.
Bryce A ManderDepartment of Psychiatry and Human Behavior, University of California Irvine, Irvine, CA, United States.ORCID https://orcid.org/0000-0002-0831-7980
Ruth M BencaDepartments of Psychiatry and Behavioral Medicine, and Translational Neuroscience, Wake Forest University School of Medicine, Winston-Salem, NC, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

How sleep medications affect brain physiology over time remains largely unknown. Prior pharmacodynamic work has established distinct spectral signatures of GABA-A receptor modulators vs. DORAs in younger or mixed adult samples. Here, we report how sleep EEG effects evolve from acute (days 1-2) to chronic (days 29-30) exposure in older adults with insomnia meeting DSM-5 criteria, and how within-person changes relate to Insomnia Severity Index (ISI). This analysis used data from a randomized, double-blind, placebo-controlled, active-comparator phase III trial (May 2016-January 2018). A subset of 249 participants was analyzed for EEG outcomes. Participants received 5 mg or 10 mg LEM (LEM5, LEM10), 6.25 mg extended-release zolpidem (ZOL), or placebo nightly for 30 days. Polysomnography was collected at baseline, after acute exposure, and after chronic exposure. Acute ZOL exposure produced significant increases in non-rapid eye movement (NREM) slow oscillation (SO), sigma, beta, and gamma power, with decreases in delta and theta compared to all treatment groups. These effects persisted with chronic exposure, alongside an alpha increase from acute to chronic exposure. LEM10 showed minimal acute effects but, with continued use, increased SO and decreased alpha power. The degree of SO power increase from acute to chronic exposure predicted improvements in ISI scores, driven by the LEM10 group. ZOL showed similar REM effects, whereas LEM5, but not LEM10, reduced REM sigma and beta power. These findings demonstrate that ZOL and LEM differentially modulate sleep EEG, with sustained SO enhancement under LEM10 linked to symptom improvement.

Indexed as

insomnialemborexantorexin antagonistssleep EEGslow oscillationsspectral powerzolpidem

Identifiers

PMID42052562
PMCPMC13116325

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.