Evidence map›Paper›PMID 25456347›Full record

ReviewPsychoneuroendocrinology2015

Translational evidence for a role of endocannabinoids in the etiology and treatment of posttraumatic stress disorder.

Alexander Neumeister, Jordan Seidel, Benjamin J Ragen, Robert H Pietrzak

Open access · greenAbstract readReview
In one paragraph

Review in Psychoneuroendocrinology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 74 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Investigational drugs in PTSD.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  4. Review
  5. Impact of self-reported cannabis use on veterans' intensive PTSD treatment outcomes.Psychological trauma : theory, research, practice and policy · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Longitudinal course of endocannabinoids andPsychological medicine · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. [Comorbidity of posttraumatic stress disorder and addiction from a biopsychosocial perspective].Neuropsychiatrie : Klinik, Diagnostik, Therapie und Rehabilitation : Organ der Gesellschaft Osterreichischer Nervenarzte und Psychiater · 2022
    Article
  15. Article
  16. Article
  17. Article
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  20. 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

4 authors at 2 institutions in 1 country.

Alexander NeumeisterDepartment of Psychiatry, New York University School of Medicine, New York, NY, USA; Department of Radiology, New York University School of Medicine, New York, NY, USA. Electronic address: alexander.neumeister@nyumc.org.
Jordan SeidelDepartment of Psychiatry, New York University School of Medicine, New York, NY, USA.
Benjamin J RagenDepartment of Psychiatry, New York University School of Medicine, New York, NY, USA.
Robert H PietrzakUnited States Department of Veterans Affairs National Center for Posttraumatic Stress Disorder, Clinical Neurosciences Division, VA Connecticut Healthcare System, West Haven, CT, USA; Department of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
New York University · USUnited States Department of Veterans Affairs · US

Funding

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
NIMH 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

introductionPosttraumatic stress disorder (PTSD) is a prevalent, chronic, and disabling anxiety disorder that may develop following exposure to a traumatic event. Despite the public health significance of PTSD, relatively little is known about the etiology or pathophysiology of this disorder, and pharmacotherapy development to date has been largely opportunistic instead of mechanism-based. Recently, an accumulating body of evidence has implicated the endocannabinoid system in the etiology of PTSD, and targets within this system are believed to be suitable for treatment development.

methodsHerein, we describe evidence from translational studies arguing for the relevance of the endocannabinoid system in the etiology of PTSD. We also show mechanisms relevant for treatment development.

resultsThere is convincing evidence from multiple studies for reduced endocannabinoid availability in PTSD. Brain imaging studies show molecular adaptations with elevated cannabinoid type 1 (CB1) receptor availability in PTSD which is linked to abnormal threat processing and anxious arousal symptoms.

conclusionOf particular relevance is evidence showing reduced levels of the endocannabinoid anandamide and compensatory increase of CB1 receptor availability in PTSD, and an association between increased CB1 receptor availability in the amygdala and abnormal threat processing, as well as increased severity of hyperarousal, but not dysphoric symptomatology, in trauma survivors. Given that hyperarousal symptoms are the key drivers of more disabling aspects of PTSD such as emotional numbing or suicidality, novel, mechanism-based pharmacotherapies that target this particular symptom cluster in patients with PTSD may have utility in mitigating the chronicity and morbidity of the disorder.

Indexed as

AnimalsBrainDisease Models, AnimalEndocannabinoidsHumansReceptor, Cannabinoid, CB1Stress Disorders, Post-TraumaticTranslational Research, BiomedicalEndocannabinoidsReceptor, Cannabinoid, CB15-Factor PTSD modelAnxious arousalEndocannabinoidsPTSDTreatment

Identifiers

PMID25456347
PMCPMC4268027
OpenAlexW2148899785

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.