Evidence map›Paper›PMID 25497473›Full record

Trial reportJournal of affective disorders2015

Pre-treatment insomnia as a predictor of single and combination antidepressant outcomes: a CO-MED report.

Sharon C Sung, Stephen R Wisniewski, James F Luther, Madhukar H Trivedi, A John Rush, COMED Study Team

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of affective disorders, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Bypassing the blues: Insomnia in the depressed post-CABG population.Annals of clinical psychiatry : official journal of the American Academy of Clinical Psychiatrists · 2020
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  5. The Association between Intranasal Esketamine and Treatment-emergent Insomnia in the Treatment of Treatment-resistant Major Depression: A Meta-analysis.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2025
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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

6 authors at 3 institutions in 2 countries.

Sharon C SungOffice of Clinical Sciences, Duke-NUS Graduate Medical School Singapore, Singapore. Electronic address: sharon.sung@duke-nus.edu.sg.
Stephen R WisniewskiEpidemiology Data Center, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
James F LutherEpidemiology Data Center, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Madhukar H TrivediDepartment of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, TX, USA.
A John RushOffice of Clinical Sciences, Duke-NUS Graduate Medical School Singapore, Singapore.
COMED Study Team
Duke-NUS Medical School · SGUniversity of Pittsburgh · USThe University of Texas Southwestern Medical Center · US

Funding

TREATMENT RESISTANT DEPRESSION-278990003N01MH090003 · NIMH · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · 1999 to 2003
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NIMH NIH HHS N01 MH090003
6 · The paper itself

Abstract

backgroundMost patients with major depressive disorder (MDD) report clinically significant sleep problems. Pre-treatment insomnia has been associated with poorer treatment outcomes in some antidepressant trials, leading to suggestions that combined treatment regimens may be more successful in this subgroup. This study investigated this question using data from the CO-MED trial.

methodsAdult outpatients with chronic and/or recurrent MDD were randomly assigned in 1:1:1 ratio to 28 weeks of single-blind, placebo-controlled antidepressant treatment with (1) escitalopram+placebo, (2) bupropion-sustained-release+escitalopram, or (3) venlafaxine-extended-release+mirtazapine. We compared baseline characteristics, tolerability, and treatment outcomes at 12 and 28 weeks for patients with and without pre-treatment insomnia.

resultsOf the 665 evaluable patients, the majority (88.3%) reported significant pre-treatment insomnia. Those with pre-treatment insomnia were more likely to be female (69.3% vs. 57.7%) and African-American (29.1% vs. 11.8%). Those with pre-treatment insomnia symptoms reported higher rates of concurrent anxiety disorders, lower rates of alcohol and substance use disorders, and greater impairment in psychosocial functioning. The two groups did not differ in either tolerability or treatment outcomes among the three antidepressant treatments.

conclusionsInsomnia symptoms, while common in patients with chronic/recurrent MDD were not predictive of response, remission, or tolerability with either single or combined antidepressant medications.

Indexed as

AdolescentAdultAgedAntidepressive AgentsAnxiety DisordersBupropionCitalopramComorbidityCyclohexanolsDelayed-Action PreparationsDrug Administration ScheduleDrug Therapy, CombinationFemaleHumansMajor Depressive DisorderMaleAntidepressive AgentsBupropionCitalopramCyclohexanolsDelayed-Action PreparationsMianserinMirtazapineVenlafaxine HydrochlorideAntidepressantInsomniaMajor depressive disorder

Identifiers

PMID25497473
PMCPMC4340746
OpenAlexW2065826161

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.