Evidence map›Paper›PMID 38870144›Full record

ArticlePloS one2024

Insomnia symptoms and neurofunctional correlates among adults receiving buprenorphine for opioid use disorder.

Augustus M White, Michelle Eglovitch, Anna Beth Parlier-Ahmad, Joseph M Dzierzewski, Morgan James, James M Bjork, F Gerard Moeller, Caitlin E Martin

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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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

8 authors.

Augustus M WhiteSchool of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States of America.ORCID 0000-0001-7794-1253
Michelle EglovitchSchool of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Anna Beth Parlier-AhmadSchool of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Joseph M DzierzewskiNational Sleep Foundation, Washington, DC, United States of America.
Morgan JamesDepartment of Psychiatry, Rutgers University, Newark, New Jersey, United States of America.ORCID 0000-0001-9298-8607
James M BjorkSchool of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States of America.ORCID 0000-0003-0593-3291
F Gerard MoellerSchool of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Caitlin E MartinSchool of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States of America.ORCID 0000-0001-5560-458X

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI BRIAN T BUCKLEY · 1988 to 2026
$47.4M
Wright Regional Center for Clinical and Translational ScienceUM1TR004360 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI FREDERICK Gerard MOELLER · 2023 to 2026
$16.3M
TRAINING IN THE PHARMACOLOGY OF ABUSED DRUGST32DA007027 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI William L. Dewey · 1985 to 2026
$14.7M
Olanzapine Augmentation in OUD Patients on Buprenorphine-Naloxone with Comorbid Symptoms of Serious Mental Illness (SMI): A Prospective Observational 8-week Pilot StudyUG1DA050207 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI ARIAS, ALBERT JOSEPH, MOELLER, FREDERICK GERARD · 2020 to 2024
$3.1M
Orexin (hypocretin) signaling in ventral tegmental area as a common mediator of sleep disturbances and drug demand in cocaine abstinenceR01DA061303 · NIDA · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Gary S. Aston-Jones, Morgan H. James · 2024 to 2026
$1.1M
Adaptation and Refinement of a Clinically Applicable Phenotypic Battery to Individualize Opioid Use Disorder Treatment for Women Through the Postpartum PeriodK23DA053507 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI MARTIN, CAITLIN EILEEN · 2021 to 2025
$1.0M
Orexin/hypocretin as a common mediator of stress and reward behavior in cocaine addictionR00DA045765 · NIDA · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI JAMES, MORGAN H. · 2021 to 2023
$747k
Health equity informed delivery of cognitive behavioral therapy for insomnia adapted for individuals with opioid use disorderR34DA058494 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI Caitlin Eileen Martin · 2024 to 2026
$699k
The Abuse Liability of a Novel Heated Tobacco Product (IQOS) and Its Feasibility as a Menthol Cigarette Substitute.F30DA057047 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI WHITE, AUGUSTUS MICHAEL · 2022 to 2025
$191k
NCATS NIH HHS UM1 TR004360NIDA NIH HHS F30 DA057047NIDA NIH HHS K23 DA053507NIDA NIH HHS R00 DA045765NIDA NIH HHS R01 DA061303NIDA NIH HHS R34 DA058494NIDA NIH HHS T32 DA007027NIDA NIH HHS UG1 DA050207NIEHS NIH HHS P30 ES005022
6 · The paper itself

Abstract

objectivesInsomnia symptoms are negatively related to opioid use disorder (OUD) treatment outcomes, possibly reflecting the influence of sleep on neurofunctional domains implicated in addiction. Moreover, the intersection between OUD recovery and sleep represents an area well-suited for the development of novel, personalized treatment strategies. This study assessed the prevalence of clinically significant insomnia symptoms and characterized its neurofunctional correlates among a clinical sample of adults with OUD receiving buprenorphine.

methodsAdults (N = 129) receiving buprenorphine for OUD from an outpatient clinic participated in a cross-sectional survey. Participants completed an abbreviated version of NIDA's Phenotyping Assessment Battery, which assessed 6 neurofunctional domains: sleep, negative emotionality, metacognition, interoception, cognition, and reward. Bivariate descriptive statistics compared those with evidence of clinically significant insomnia symptoms (Insomnia Severity Index [ISI] score of ≥11) to those with minimal evidence of clinically significant insomnia symptoms (ISI score of ≤10) across each of the neurofunctional domains.

resultsRoughly 60% of participants reported clinically significant insomnia symptoms (ISI score of ≥11). Experiencing clinically significant insomnia symptoms was associated with reporting greater levels of depression, anxiety, post-traumatic stress, stress intolerance, unhelpful metacognition, and interoceptive awareness (ps<0.05). Participants with evidence of clinically significant insomnia were more likely to report that poor sleep was interfering with their OUD treatment and that improved sleep would assist with their treatment (ps<0.05).

conclusionsInsomnia was prevalent among adults receiving buprenorphine for OUD. Insomnia was associated with neurofunctional performance, which may impact OUD treatment trajectories. Our findings indicate potential targets in the development of personalized treatment plans for patients with co-morbid insomnia and OUD. To inform the development of novel treatment strategies, more research is needed to understand the potential mechanistic links between sleep disturbances and substance use.

Indexed as

BuprenorphineOpioid-Related DisordersSleep Initiation and Maintenance DisordersAdultCognitionCross-Sectional StudiesFemaleHumansInteroceptionMaleMiddle AgedOpiate Substitution TreatmentRewardSleepBuprenorphine

Identifiers

PMID38870144
PMCPMC11175529

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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.