Evidence map›Paper›PMID 26432420›Full record

ArticleBiological psychiatry2016

Reduced Brain Cannabinoid Receptor Availability in Schizophrenia.

Mohini Ranganathan, Jose Cortes-Briones, Rajiv Radhakrishnan, Halle Thurnauer, Beata Planeta, Patrick Skosnik, Hong Gao, David Labaree, Alexander Neumeister, Brian Pittman and 4 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05105542 (Muscarinic M1 Receptor Availability and Cognition in Schizophrenia), which is not on this map. Cited by 69 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 3 pooled it
6.2field-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.

NCT05105542 phase1completednot on this mapstarted 2021, after this paper: background citation

Muscarinic M1 Receptor Availability and Cognition in Schizophrenia

TypeinterventionalSponsorYale UniversityRan2021 to 2023Enrolled18ConditionsSchizophrenia, Schizoaffective Disorder, HealthyArms11C-EMO - A Novel PET Radiotracer for Muscarinic M1 Receptor, PET Scan
3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 3 syntheses or guidelines pooled it, 124 citations in OpenAlex.

  1. Pooled it
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  3. Pooled it
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  9. Gray Matter Volume Loss in Parkinson's Disease Psychosis and Cannabinoid Receptor Gene Expression in the Brain.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
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9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 1 country.

Mohini RanganathanSchizophrenia and Neuropharmacology Research Group, Veterans Affairs Connecticut Healthcare System, West Haven; Abraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven; Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut. Electronic address: mohini.ranganathan@yale.edu.
Jose Cortes-BrionesSchizophrenia and Neuropharmacology Research Group, Veterans Affairs Connecticut Healthcare System, West Haven; Abraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven; Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut.
Rajiv RadhakrishnanSchizophrenia and Neuropharmacology Research Group, Veterans Affairs Connecticut Healthcare System, West Haven; Abraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven; Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut.
Halle ThurnauerSchizophrenia and Neuropharmacology Research Group, Veterans Affairs Connecticut Healthcare System, West Haven; Abraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven; Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut.
Beata PlanetaAbraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven; Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut; Positron Emission Tomography Center, Yale University School of Medicine, New Haven, Connecticut.
Patrick SkosnikSchizophrenia and Neuropharmacology Research Group, Veterans Affairs Connecticut Healthcare System, West Haven; Abraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven; Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut.
Hong GaoPositron Emission Tomography Center, Yale University School of Medicine, New Haven, Connecticut.
David LabareePositron Emission Tomography Center, Yale University School of Medicine, New Haven, Connecticut.
Alexander NeumeisterMolecular Imaging Program for Mood and Anxiety Disorders, New York University Langone Medical Center, New York, New York.
Brian PittmanAbraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven; Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut; Positron Emission Tomography Center, Yale University School of Medicine, New Haven, Connecticut.
Toral SurtiDepartment of Psychiatry, Yale University School of Medicine, New Haven, Connecticut.
Yiyun HuangPositron Emission Tomography Center, Yale University School of Medicine, New Haven, Connecticut.
Richard E CarsonPositron Emission Tomography Center, Yale University School of Medicine, New Haven, Connecticut.
Deepak Cyril D'SouzaSchizophrenia and Neuropharmacology Research Group, Veterans Affairs Connecticut Healthcare System, West Haven; Abraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven; Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut.
Yale University · USConnecticut Mental Health Center · USItron (United States) · USNYU Langone Health · USVA Connecticut Healthcare System · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Schizophrenia Research FellowshipR25MH071584 · NIMH · YALE UNIVERSITY · PI Christopher John Pittenger · 2005 to 2026
$4.4M
CB1 Receptor PET Imaging Reveals Gender Differencesin PTSDR01MH096876 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEUMEISTER, ALEXANDER · 2012 to 2014
$921k
Imaging Brain Cannabinoid Receptors in Cannabis Dependence, Withdrawal and AbstinR21DA030702 · NIDA · YALE UNIVERSITY · PI D'SOUZA, DEEPAK CYRIL, SKOSNIK, PATRICK DAVID · 2011 to 2012
$456k
Imaging Brain Cannabinoid Receptors (CB1) in SchizophreniaR21MH094961 · NIMH · YALE UNIVERSITY · PI D'SOUZA, DEEPAK CYRIL · 2012 to 2013
$383k
NCATS NIH HHS UL1 TR001863NIDA NIH HHS R21 DA030702NIMH NIH HHS R01 MH096876NIMH NIH HHS R21 MH094961NIMH NIH HHS R25 MH071584
6 · The paper itself

Abstract

backgroundSeveral lines of evidence suggest the presence of abnormalities in the endocannabinoid (eCB) system in schizophrenia (SCZ). However, there are limited in vivo measures of the eCB system in SCZ.

methodsTwenty five male SCZ subjects (SCZs) (18 antipsychotic treated and 7 antipsychotic free) were compared with 18 age-matched male healthy control subjects (HCs). Subjects underwent one positron emission tomography scan each with the cannabinoid receptor-1 (CB1R) selective radiotracer [(11)C]OMAR on the high resolution research tomography scanner. Regional volume of distribution (VT) values were determined using kinetic modeling of positron emission tomography data as a measure of CB1R availability. Group differences in mean composite [(11)C]OMAR VT values were compared between SCZs and HCs. Exploratory comparisons of CB1R availability within 15 brain regions were also conducted. All analyses were covaried for age and body mass index.

resultsSCZs showed significantly (p = .02) lower composite [(11)C]OMAR VT relative to HCs (~12% difference, effect size d = .73). [(11)C]OMAR VT was significantly (all ps < .05) lower in SCZs in the amygdala, caudate, posterior cingulate cortex, hippocampus, hypothalamus, and insula. Composite [11]OMAR VT was HCs > antipsychotic treated SZCs > antipsychotic free SZCs. Furthermore, composite [(11)C]OMAR VT was greater in HCs than SCZ smokers (n = 11) and SCZ nonsmokers (n = 14).

conclusionsCB1R availability is lower in male SCZ subjects compared with HCs. Furthermore, antipsychotics and tobacco use may increase CB1R availability in this population. The findings of the study provide further evidence supporting the hypothesis that alterations in the eCB system might contribute to the pathophysiology of SCZ.

Indexed as

AdultAntipsychotic AgentsHumansMaleMiddle AgedPositron-Emission TomographyRadiopharmaceuticalsReceptor, Cannabinoid, CB1SchizophreniaSmokingYoung AdultAntipsychotic AgentsRadiopharmaceuticalsReceptor, Cannabinoid, CB1AntipsychoticsCannabinoidCB(1)ROMARSchizophreniaSmoking

Identifiers

PMID26432420
PMCPMC4884543
OpenAlexW1160137332

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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.