Evidence map›Paper›PMID 25411966›Full record

ArticlePloS one2014

Striatal dopamine D2/3 receptor availability in treatment resistant depression.

Bart P de Kwaasteniet, Chedwa Pinto, Henricus G Ruhé, Eric H G Ruhé, Guido A van Wingen, Jan Booij, Damiaan Denys

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  4. Review
  5. Article
  6. Article
  7. The relationship between the dopaminergic system and depressive symptoms in cervical dystonia.European journal of nuclear medicine and molecular imaging · 2017
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Bart P de KwaastenietDepartment of Psychiatry, Academic Medical Center, Amsterdam, the Netherlands; Brain Imaging Center, Academic Medical Center, Amsterdam, the Netherlands.
Chedwa PintoDepartment of Psychiatry, MC groep, Lelystad, the Netherlands.
Henricus G Ruhé
Eric H G RuhéDepartment of Psychiatry, Academic Medical Center, Amsterdam, the Netherlands; Brain Imaging Center, Academic Medical Center, Amsterdam, the Netherlands; University of Groningen, University Medical Center Groningen, Mood and Anxiety Disorders, Department of Psychiatry, Groningen, the Netherlands.
Guido A van WingenDepartment of Psychiatry, Academic Medical Center, Amsterdam, the Netherlands; Brain Imaging Center, Academic Medical Center, Amsterdam, the Netherlands.
Jan BooijBrain Imaging Center, Academic Medical Center, Amsterdam, the Netherlands; Department of Nuclear Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Damiaan DenysDepartment of Psychiatry, Academic Medical Center, Amsterdam, the Netherlands; Brain Imaging Center, Academic Medical Center, Amsterdam, the Netherlands; The Institute for Neuroscience, an institute of the Royal Netherlands Academy of Arts and Sciences, Amsterdam, the Netherlands.
Academic Medical Center · NLRoyal Netherlands Academy of Arts and Sciences · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies demonstrated improvement of depressive symptoms in treatment resistant depression (TRD) after administering dopamine agonists which suggest abnormal dopaminergic neurotransmission in TRD. However, the role of dopaminergic signaling through measurement of striatal dopamine D(2/3) receptor (D2/3R) binding has not been investigated in TRD subjects. We used [(123)I]IBZM single photon emission computed tomography (SPECT) to investigate striatal D2/3R binding in TRD. We included 6 severe TRD patients, 11 severe TRD patients on antipsychotics (TRD AP group) and 15 matched healthy controls. Results showed no significant difference (p = 0.75) in striatal D2/3R availability was found between TRD patients and healthy controls. In the TRD AP group D2/3R availability was significantly decreased (reflecting occupancy of D2/3Rs by antipsychotics) relative to TRD patients and healthy controls (p<0.001) but there were no differences in clinical symptoms between TRD AP and TRD patients. This preliminary study therefore does not provide evidence for large differences in D2/3 availability in severe TRD patients and suggests this TRD subgroup is not characterized by altered dopaminergic transmission. Atypical antipsychotics appear to have no clinical benefit in severe TRD patients who remain depressed, despite their strong occupancy of D2/3Rs.

Indexed as

AdolescentAdultAgedAntipsychotic AgentsCase-Control StudiesCorpus StriatumDepressive Disorder, Treatment-ResistantDopamine D2 Receptor AntagonistsFemaleHumansIodobenzenesMaleMiddle AgedRadiopharmaceuticalsReceptors, Dopamine D2Receptors, Dopamine D3Antipsychotic AgentsDopamine D2 Receptor AntagonistsidobenzamideIodobenzenesRadiopharmaceuticalsReceptors, Dopamine D2Receptors, Dopamine D3

Identifiers

PMID25411966
PMCPMC4239080
OpenAlexW1980894681

What OpenQuestion holds

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LicenceCC BY
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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.