Evidence map›Paper›PMID 24767003›Full record

Trial reportJournal of affective disorders2014

Antidepressant treatment history as a predictor of response to scopolamine: clinical implications.

Jessica S Ellis, Carlos A Zarate, David A Luckenbaugh, Maura L Furey

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of affective disorders, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04211961 (A Randomised Double-Blinded Placebo-Controlled Trial to Assess the Efficacy and Safety of Scopolamine Compared to Placebo in Individuals With Bipolar Disorder Who Are Experiencing a Depressive Episode), which is not on this map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 8% 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.

NCT04211961 phase2completednot on this mapstarted 2021, after this paper: background citation

A Randomised Double-Blinded Placebo-Controlled Trial to Assess the Efficacy and Safety of Scopolamine Compared to Placebo in Individuals With Bipolar Disorder Who Are Experiencing a Depressive Episode

TypeinterventionalSponsorDr. Brian HallahanRan2021 to 2024Enrolled55ConditionsBipolar Disorder DepressionArmsPlacebo / Saline, Scopolamine
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. The effect of scopolamine on memory and attention: a systematic review and meta-analysis.European psychiatry : the journal of the Association of European Psychiatrists · 2025
    Pooled it
  2. Pooled it
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  7. Article
  8. Normalization of impaired emotion inhibition in bipolar disorder mediated by cholinergic neurotransmission in the cingulate cortex.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
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  18. Rodent models of treatment-resistant depression.European journal of pharmacology · 2015
    Review
  19. Review
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

4 authors at 2 institutions in 1 country.

Jessica S EllisNational Institutes of Health/National Institute of Mental Health,Experimental Therapeutics and Pathophysiology Branch, 10 Center Dr., Building 10/CRC, Room 7-5561, Bethesda, MD 20814-9692, USA. Electronic address: brockmeyerjs@mail.nih.gov.
Carlos A ZarateNational Institutes of Health/National Institute of Mental Health,Experimental Therapeutics and Pathophysiology Branch, 10 Center Dr., Building 10/CRC, Room 7-5561, Bethesda, MD 20814-9692, USA; National Institutes of Health/National Institute of Mental Health, Experimental Therapeutics and Pathophysiology Branch, 10 Center Dr., Building 10/CRC, Bethesda, MD, 20814-9692, USA.
David A LuckenbaughNational Institutes of Health/National Institute of Mental Health,Experimental Therapeutics and Pathophysiology Branch, 10 Center Dr., Building 10/CRC, Room 7-5561, Bethesda, MD 20814-9692, USA; National Institutes of Health/National Institute of Mental Health, Experimental Therapeutics and Pathophysiology Branch, 10 Center Dr., Building 10/CRC, Bethesda, MD, 20814-9692, USA.
Maura L FureyNational Institutes of Health/National Institute of Mental Health,Experimental Therapeutics and Pathophysiology Branch, 10 Center Dr., Building 10/CRC, Room 7-5561, Bethesda, MD 20814-9692, USA; National Institutes of Health/National Institute of Mental Health, Experimental Therapeutics and Pathophysiology Branch, 10 Center Dr., Building 10/CRC, Bethesda, MD, 20814-9692, USA.
National Institute of Mental Health · USNational Institutes of Health · US

Funding

Cholinergic Modulation of Cognition and Emotion in Mood DisordersZIAMH002813 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI ZARATE, CARLOS · 2009 to 2014
$3.4M
Cholinergic System--Cognition/Emotion in Mood DisZ01MH002813 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI FUREY, MAURA L. · 2003 to 2008
$851k
Intramural NIH HHS Z99 MH999999NIMH NIH HHS Z01-MH002813
6 · The paper itself

Abstract

backgroundThe intravenous administration of scopolamine produces rapid antidepressant effects. Generally, failing multiple previous antidepressant trials is associated with a poor prognosis for response to future medications. This study evaluated whether treatment history predicts antidepressant response to scopolamine.

methodsTreatment resistant patients (2 failed medication trials) (n=31) and treatment naïve patients (no exposure to psychotropic medication) (n=31) with recurrent major depressive or bipolar disorder participated in a double-blind, placebo-controlled, crossover clinical trial. Following a placebo lead-in, participants randomly received P/S or S/P (P=3 placebo; S=3 scopolamine (4ug/kg) sessions 3 to 5 days apart). The Montgomery-Asberg Depression Rating Scale (MADRS) was the primary outcome measure. A linear mixed model was used to examine the interaction between clinical response and treatment history, adjusting for baseline MADRS.

resultsTreatment resistant and treatment naïve subjects combined responded significantly to scopolamine compared to placebo (F=15.06, p<0.001). Reduction in depressive symptoms was significant by the first post-scopolamine session (F=42.75, p<0.001). A treatment history by scopolamine session interaction (F=3.37, p=0.04) indicated treatment naïve subjects had lower MADRS scores than treatment resistant patients; this was significant after the second scopolamine infusion (t=2.15, p=0.03). LIMITATIONS: Post-hoc analysis: Also, we used a single regimen to administer scopolamine, and smokers were excluded from the sample, limiting generalizability.

conclusionsTreatment naïve and treatment resistant patients showed improved clinical symptoms following scopolamine, while those who were treatment naïve showed greater improvement. Scopolamine rapidly reduces symptoms in both treatment history groups, and demonstrates sustained improvement even in treatment resistant patients.

Indexed as

AdolescentAdultAntidepressive AgentsBipolar DisorderCross-Over StudiesDouble-Blind MethodFemaleHumansMajor Depressive DisorderMaleMiddle AgedPsychiatric Status Rating ScalesResearch DesignScopolamineYoung AdultAntidepressive AgentsScopolamineAntidepressantDepressionScopolamineTreatment historyTreatment resistant

Identifiers

PMID24767003
PMCPMC4030406
OpenAlexW2051925083

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.