Evidence map›Paper›PMID 24914549›Full record

Trial reportPloS one2014

Changes in QTc interval in the citalopram for agitation in Alzheimer's disease (CitAD) randomized trial.

Lea T Drye, David Spragg, D P Devanand, Constantine Frangakis, Christopher Marano, Curtis L Meinert, Jacobo E Mintzer, Cynthia A Munro, Gregory Pelton, Bruce G Pollock and 9 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00898807 (A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease), which is not on this map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.9field-weighted citation impact, top 4% 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.

NCT00898807 phase3completednot on this map

A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease

TypeinterventionalSponsorJHSPH Center for Clinical TrialsRan2009 to 2013Enrolled186ConditionsAlzheimer's Disease, AgitationArmscitalopram, placebo
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
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  5. The Effect of Agomelatine in Behavioral and Psychological Symptoms of Dementia.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2022
    Article
  6. Article
  7. Diagnosis and Treatment of Alzheimer's Disease:: An Update.Delaware journal of public health · 2021
    Article
  8. Observational
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  10. Review
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  19. Characterizing Highly Benefited Patients in Randomized Clinical Trials.The international journal of biostatistics · 2017
    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

19 authors at 10 institutions in 2 countries.

Lea T DryeDepartment of Epidemiology and Center for Clinical Trials, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
David SpraggElectrophysiology Laboratory, Johns Hopkins Hospital and Johns Hopkins Bayview Medical Center, Baltimore, Maryland, United States of America.
D P DevanandDivision of Geriatric Psychiatry, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America.
Constantine FrangakisDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Christopher MaranoDivision of Geriatric Psychiatry and Neuropsychiatry, Johns Hopkins University School of Medicine, Johns Hopkins Bayview Medical Center, Baltimore, Maryland, United States of America.
Curtis L MeinertDepartments of Epidemiology and Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Jacobo E MintzerClinical Biotechnology Research Institute, Roper St. Francis Healthcare, Department of Health Studies, Medical University of South Carolina, Ralph H. Johnson VA Medical Center, Charleston, South Carolina, United States of America.
Cynthia A MunroDepartments of Psychiatry and Behavioral Sciences and Neurology, Johns Hopkins Bayview and Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Gregory PeltonDivision of Geriatric Psychiatry, New York State Psychiatric Institute, College of Physicians and Surgeons of Columbia University, New York, New York, United States of America.
Bruce G PollockCampbell Family Mental Health Research Institute, Division of Geriatric Psychiatry and Centre for Addiction and Mental Health, University of Toronto, Toronto, Ontario, Canada.
Anton P PorsteinssonAlzheimer's Disease Care, Research and Education Program (AD-CARE), University of Rochester School of Medicine and Dentistry, Rochester, New York, United States of America.
Peter V RabinsDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine and Johns Hopkins Hospital, Baltimore, Maryland, United States of America.
Paul B RosenbergDepartment of Psychiatry and Behavioral Sciences, John Hopkins University School of Medicine and Johns Hopkins Bayview Medical Center, Baltimore, Maryland, United States of America.
Lon S SchneiderDepartments of Psychiatry, Neurology, and Gerontology, Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
David M ShadeDepartments of Medicine (Pulmonary) and Epidemiology and Center for Clinical Trials, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
Daniel WeintraubDepartments of Psychiatry and Neurology, Perelman School of Medicine at the University of Pennsylvania, Parkinson's Disease Research, Education and Clinical Center (PADRECC), Mental Illness Research, Education and Clinical Center (MIRECC), Philadelphia Veterans Affairs Medical Center, Philadelphia, Pennsylvania, United States of America.
Jerome YesavageAging Clinical Research Center, Mental Illness Research Education and Clinical Center, Veterans Affairs Palo Alto Health Care System, Departments of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, California, United States of America.
Constantine G LyketsosMemory and Alzheimer's Treatment Center, Department of Psychiatry and Behavioral Sciences, Johns Hopkins Bayview and Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.
CitAD Research Group
Johns Hopkins University · USColumbia University · USJohns Hopkins Bayview Medical Center · USJohns Hopkins Hospital · USMedical University of South Carolina · USUniversity of Pennsylvania · USUniversity of Rochester · USUniversity of Southern California · USUniversity of Toronto · CAVA Palo Alto Health Care System · US

Funding

VASCULAR RISK AND COGNITIVE STATUS IN A LATINO POPULATIONP50AG005142 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KIM, PAUL E · 1985 to 2019
$41.0M
Citalopram Treatment for Agitation in Alzheimer DementiaR01AG031348 · NIA · JOHNS HOPKINS UNIVERSITY · PI LYKETSOS, CONSTANTINE G · 2008 to 2012
$7.9M
Insulin Resistance in Late-Life DepressionK23MH095971 · NIMH · JOHNS HOPKINS UNIVERSITY · PI MARANO, CHRISTOPHER · 2012 to 2016
$903k
NIA NIH HHS P50 AG005142NIA NIH HHS R01 AG031348NIA NIH HHS R01AG031348NIMH NIH HHS K23 MH095971
6 · The paper itself

Abstract

backgroundA Food and Drug Administration (FDA) safety communication in August 2011 warned that citalopram was associated with a dose dependent risk of QT prolongation and recommended dose restriction in patients over the age of 60 but did not provide data for this age group.

methodsCitAD was a randomized, double-masked, placebo-controlled, multicenter clinical trial for agitation in Alzheimer's disease (AD). Participants were assigned to citalopram (target dose of 30 mg/day) or placebo in a 1 ∶ 1 ratio. 186 people, 181 of whom were over the age of 60, having probable AD with clinically significant agitation were recruited from September 2009 to January 2013. After the FDA safety communication about citalopram, ECG was added to the required study procedures before enrollment and repeated at week 3 to monitor change in QTc interval. Forty-eight participants were enrolled after enhanced monitoring began.

resultsCitalopram treatment was associated with a larger increase in QTc interval than placebo (difference in week 3 QTc adjusting for baseline QTc: 18.1 ms [95% CI: 6.1, 30.1]; p = 0.004). More participants in the citalopram group had an increase ≥ 30 ms from baseline to week 3 (7 in citalopram versus 1 in placebo; Fisher's exact p = 0.046), but only slightly more in the citalopram group met a gender-specific threshold for prolonged QTc (450 ms for males; 470 ms for females) at any point during follow-up (3 in citalopram versus 1 in placebo, Fisher's exact p = 0.611). One of the citalopram participants who developed prolonged QTc also displayed ventricular bigeminy. No participants in either group had a cardiovascular-related death.

conclusionCitalopram at 30 mg/day was associated with improvement in agitation in patients with AD but was also associated with QT prolongation.

trial registrationClinicalTrials.gov NCT00898807.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseAntidepressive Agents, Second-GenerationCardiotoxicityCitalopramDouble-Blind MethodFemaleHeart RateHumansMalePsychomotor AgitationAntidepressive Agents, Second-GenerationCitalopram

Identifiers

PMID24914549
PMCPMC4051660
OpenAlexW1975308821

What OpenQuestion holds

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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.