Evidence map›Paper›PMID 21841458›Full record

Trial reportThe American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry2011

Serotonin transporter occupancy and the functional neuroanatomic effects of citalopram in geriatric depression.

Gwenn S Smith, Alan Kahn, Julia Sacher, Pablo Rusjan, Thilo van Eimeren, Alastair Flint, Alan A Wilson

Abstract readClinical Trial
In one paragraph

Trial report in The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. SLC6A4 polymorphisms and age of onset in late-life depression on treatment outcomes with citalopram: a Sequenced Treatment Alternatives to Relieve Depression (STAR*D) report.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry · 2014
    Trial
  4. Trial
  5. Trajectories of late-life depression: insights from molecular imaging.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Positron emission tomography molecular imaging in late-life depression.Journal of geriatric psychiatry and neurology · 2014
    Review
  10. Review
  11. 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

7 authors at 5 institutions in 3 countries.

Gwenn S SmithDivision of Geriatric Psychiatry and Neuropsychiatry, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA. gsmith95@jhmi.edu
Alan Kahn
Julia Sacher
Pablo Rusjan
Thilo van Eimeren
Alastair Flint
Alan A Wilson
Centre for Addiction and Mental Health · CAUniversity Health Network · CAJohns Hopkins University · USMax Planck Institute for Human Cognitive and Brain Sciences · DEUniversity of Toronto · CA

Funding

Serotonin Modulation in Geriatric DepressionR01MH064823 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SMITH, GWENN S. · 2003 to 2006
$1.9M
MONOAMINERGIC FUNCTION IN GERIATRIC NEUROPSYCHIATRYK02MH001621 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SMITH, GWENN S · 1998 to 2008
$884k
NIMH NIH HHS K02 MH001621NIMH NIH HHS MH01621NIMH NIH HHS MH64823NIMH NIH HHS R01 MH064823
6 · The paper itself

Abstract

objectivesThe functional neuroanatomic changes associated with selective serotonin reuptake inhibitor (SSRI) treatment have been the focus of positron emission tomography (PET) studies of cerebral glucose metabolism in geriatric depression.

designTo evaluate the underlying neurochemical mechanisms, both cerebral glucose metabolism and serotonin transporter (SERT) availability were measured before and during treatment with the SSRI, citalopram. It was hypothesized that SERT occupancy would be observed in cortical and limbic brain regions that have shown metabolic effects, as well as striatal and thalamic regions that have been implicated in prior studies in midlife patients.

settingPsychiatric outpatient clinic.

participantsSeven depressed patients who met Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria for current major depressive episode were enrolled.

interventionPatients underwent a 12-week open-label trial of the SSRI, citalopram. MEASUREMENTS: Patients underwent high-resolution research tomography PET scans to measure changes in cerebral glucose metabolism and SERT occupancy by citalopram treatment (after 8-10 weeks of treatment).

resultsThree different tracer kinetic models were applied to the [¹¹C]-DASB region-of-interest data and yielded similar results of an average of greater than 70% SERT occupancy in the striatum and thalamus during citalopram treatment. Voxel-wise analyses showed significant SERT occupancy in these regions, as well as cortical (e.g., anterior cingulate, superior and middle frontal, precuneus, and limbic (parahippocampal gyrus) areas that also showed reductions in glucose metabolism.

conclusionThe findings suggest that cortical and limbic SERT occupancy may be an underlying mechanism for the regional cerebral metabolic effects of citalopram in geriatric depression.

Indexed as

AgedAniline CompoundsBrainCitalopramDepressionFemaleGlucoseHumansMalePositron-Emission TomographyRadioligand AssaySelective Serotonin Reuptake InhibitorsSerotonin Plasma Membrane Transport ProteinsSulfides3-amino-4-(2-dimethylaminomethylphenylsulfanyl)benzonitrileAniline CompoundsCitalopramGlucoseSelective Serotonin Reuptake InhibitorsSerotonin Plasma Membrane Transport ProteinsSulfides

Identifiers

PMID21841458
PMCPMC3968900
OpenAlexW2144357260

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.