Evidence map›Paper›PMID 24820537›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Cannabinoid type 1 receptor availability in the amygdala mediates threat processing in trauma survivors.

Robert H Pietrzak, Yiyun Huang, Stefani Corsi-Travali, Ming-Qiang Zheng, Shu-fei Lin, Shannan Henry, Marc N Potenza, Daniele Piomelli, Richard E Carson, Alexander Neumeister

RetractedOpen access · bronzeAbstract readRetracted Publication
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.0field-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.

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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  5. CBInternational journal of molecular sciences · 2020
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  13. Article
  14. Cannabinoid Receptor 1 Positive Allosteric Modulators for Posttraumatic Stress Disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Robert H Pietrzak1] Clinical Neurosciences Division, National Center for Posttraumatic Stress Disorder, Veterans Affairs Connecticut Healthcare System, West Haven, CT, USA [2] Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Yiyun HuangDepartment of Diagnostic Radiology, Yale University School of Medicine, New Haven, CT, USA.
Stefani Corsi-TravaliDepartments of Psychiatry and Radiology, New York University School of Medicine, New York, NY, USA.
Ming-Qiang ZhengDepartment of Diagnostic Radiology, Yale University School of Medicine, New Haven, CT, USA.
Shu-fei LinDepartment of Diagnostic Radiology, Yale University School of Medicine, New Haven, CT, USA.
Shannan HenryDepartment of Diagnostic Radiology, Yale University School of Medicine, New Haven, CT, USA.
Marc N PotenzaDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Daniele PiomelliAnatomy & Neurobiology School of Medicine, University of California, Irvine, Irvine, CA, USA.
Richard E CarsonDepartment of Diagnostic Radiology, Yale University School of Medicine, New Haven, CT, USA.
Alexander NeumeisterDepartments of Psychiatry and Radiology, New York University School of Medicine, New York, NY, USA.
Yale University · USNew York University · USUniversity of California, Irvine · USVA Connecticut Healthcare System · US

Funding

YALE UNIVERSITY CLINICAL AND TRANSLATIONAL SCIENCE AWARD PROGRAMUL1RR024139 · NCRR · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2006 to 2011
$56.8M
Yale University Clinical and Translational Science Award ProgramUL1TR000142 · NCATS · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2012 to 2015
$31.8M
CB1 Receptor PET Imaging Reveals Gender Differencesin PTSDR01MH096876 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEUMEISTER, ALEXANDER · 2012 to 2014
$921k
Kappa Opioid Receptor Imaging in PTSDR21MH096105 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEUMEISTER, ALEXANDER · 2012 to 2014
$746k
KOR DepressionR01MH102566 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEUMEISTER, ALEXANDER · 2014 to 2014
$438k
Serotonin 1B Receptor Imaging in PTSD with and without Co-morbid DepressionR21MH085627 · NIMH · YALE UNIVERSITY · PI NEUMEISTER, ALEXANDER · 2009 to 2010
$411k
A mGlu2/3 agonist in the treatment of PTSDR34MH102871 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEUMEISTER, ALEXANDER · 2014 to 2014
$18k
NCATS NIH HHS UL1 TR000142NCRR NIH HHS UL1 RR024139NIMH NIH HHS R01 MH096876NIMH NIH HHS R01MH096876NIMH NIH HHS R01 MH102566NIMH NIH HHS R01MH102566NIMH NIH HHS R21 MH085627NIMH NIH HHS R21MH085627NIMH NIH HHS R21 MH096105NIMH NIH HHS R21MH096105NIMH NIH HHS R34 MH102871
6 · The paper itself

Abstract

Attentional bias to threat is a key endophenotype that contributes to the chronicity of trauma-related psychopathology. However, little is known about the neurobiology of this endophenotype and no known in vivo molecular imaging study has been conducted to evaluate candidate receptor systems that may be implicated in this endophenotype or the phenotypic expression of trauma-related psychopathology that comprises threat (ie, re-experiencing, avoidance, and hyperarousal) and loss (ie, emotional numbing, depression/dysphoria, generalized anxiety) symptomatology. Using the radioligand [(11)C]OMAR and positron emission tomography (PET), we evaluated the relationship between in vivo cannabinoid receptor type 1 (CB1) receptor availability in the amygdala, and performance on a dot-probe measure of attentional bias to threat, and clinician interview-based measures of trauma-related psychopathology. The sample comprised adults presenting with a broad spectrum of trauma-related psychopathology, ranging from nontrauma-exposed, psychiatrically healthy adults to trauma-exposed adults with severe trauma-related psychopathology. Results revealed that increased CB1 receptor availability in the amygdala was associated with increased attentional bias to threat, as well as increased severity of threat, but not loss, symptomatology; greater peripheral anandamide levels were associated with decreased attentional bias to threat. A mediation analysis further suggested that attentional bias to threat mediated the relationship between CB1 receptor availability in the amygdala and severity of threat symptomatology. These data substantiate a key role for compromised endocannabinoid function in mediating both the endophenotypic and phenotypic expression of threat symptomatology in humans. They further suggest that novel pharmacotherapies that target the CB1 system may provide a more focused, mechanism-based approach to mitigating this core aspect of trauma-related psychopathology.

Indexed as

AdultAmygdalaArachidonic AcidsAttentionCarbon RadioisotopesEndocannabinoidsFearFemaleHumansInterview, PsychologicalMagnetic Resonance ImagingMaleMiddle AgedNeuropsychological TestsPolyunsaturated AlkamidesPositron-Emission TomographyanandamideArachidonic AcidsCarbon RadioisotopesEndocannabinoidsPolyunsaturated AlkamidesRadiopharmaceuticalsReceptor, Cannabinoid, CB1

Identifiers

PMID24820537
PMCPMC4207337
OpenAlexW1967402002

What OpenQuestion holds

Textmetadata
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.