Evidence map›Paper›PMID 34670131›Full record

Trial reportJournal of affective disorders2022

Longitudinal study of impact of medication for opioid use disorder on Hamilton Depression Rating Scale.

Kesheng Wang, Toni DiChiacchio, Wei Fang, Laura Lander, Judith Feinberg, Changchun Xie, Erin L Winstanley, Ubolrat Piamjariyakul

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of affective disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Article
  3. 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

8 authors at 3 institutions in 1 country.

Kesheng WangDepartment of Family and Community Health, School of Nursing, Health Sciences Center, West Virginia University, Morgantown, WV 26506, USA. Electronic address: kesheng.wang@hsc.wvu.edu.
Toni DiChiacchioSchool of Nursing, Health Sciences Center, West Virginia University, Morgantown, WV 26506, USA.
Wei FangWest Virginia Clinical and Translational Science Institute, Health Sciences Center, West Virginia University, Morgantown, WV 26506, USA.
Laura LanderDepartment of Behavioral Medicine and Psychiatry, School of Medicine, Rockefeller Neuroscience Institute, Morgantown, WV 26506, USA.
Judith FeinbergDepartment of Behavioral Medicine and Psychiatry, School of Medicine, Rockefeller Neuroscience Institute, Morgantown, WV 26506, USA; Department of Neuroscience, West Virginia University, Morgantown, WV 26506, USA.
Changchun XieDivision of Biostatistics and Bioinformatics, Department of Environmental and Public Health Sciences, University of Cincinnati, Cincinnati, OH 45267, USA.
Erin L WinstanleyDepartment of Behavioral Medicine and Psychiatry, School of Medicine, Rockefeller Neuroscience Institute, Morgantown, WV 26506, USA; Department of Neuroscience, West Virginia University, Morgantown, WV 26506, USA.
Ubolrat PiamjariyakulSchool of Nursing, Health Sciences Center, West Virginia University, Morgantown, WV 26506, USA.
West Virginia University · USBlanchette Rockefeller Neurosciences Institute · USUniversity of Cincinnati · US

Funding

Project-008UG1DA049436 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jane M. Liebschutz, Erin L Winstanley · 2019 to 2026
$10.5M
NIDA NIH HHS UG1 DA049436
6 · The paper itself

Abstract

objectiveThis study aimed to evaluate the longitudinal treatment effect on depression measured by Hamilton Depression Rating Scale (HAM-D) score in a randomized clinical trial for the treatment of opioid use disorder (OUD).

methodsWe conducted a secondary data analysis of data from the National Institute on Drug Abuse's Clinical Trials Network Protocol-0051. Patients with OUD (N = 570) were randomized to receive buprenorphine/naloxone (BUP-NX, n = 287) or extended-release naltrexone injection (XR-NTX, n = 283). The HAM-D score was completed at baseline and follow-up visit up to 36 weeks. A linear mixed model analysis was performed for log transformed HAM-D score and a generalized linear mixed model analysis was conducted for depression status.

resultsCompared with BUP-NX, subjects randomized to XR-NTX had higher HAM-D scores at weeks 1 and 3 (p<0.05). There were significant interactions between treatment and visit on HAM-D score and depression status during the first four weeks of treatments in individuals without lifetime major depressive disorder (MDD). Past year cocaine use was associated with HAM-D score and depression status just in individuals without MDD, whereas past year cannabis use was associated with HAM-D score and depression status just in individuals with MDD. Past year amphetamine use was associated with HAM-D score just in individuals without MDD, however, lifetime anxiety was associated with HAM-D scores regardless of MDD.

conclusionWhen prescribing XR-NTX, particularly in the first month of treatment, it is essential to monitor for depressive symptoms. Screening for depression and multiple substance abuse may help clinicians identify appropriate treatment.

Indexed as

Major Depressive DisorderOpioid-Related DisordersDelayed-Action PreparationsDepressionHumansInjections, IntramuscularLongitudinal StudiesNarcotic AntagonistsDelayed-Action PreparationsNarcotic AntagonistsDepressionGeneralized linear mixed modelHAM-DLinear mixed modelOpioid use disorderSubstance use

Identifiers

PMID34670131
PMCPMC12882690
OpenAlexW3205768753

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.