Evidence map›Paper›PMID 36764853›Full record

ArticleBiological psychiatry2023

Differences in Quantification of the Metabotropic Glutamate Receptor 5 Across Bipolar Disorder and Major Depressive Disorder.

Sophie E Holmes, Ruth H Asch, Margaret T Davis, Nicole DellaGioia, Neha Pashankar, Jean-Dominique Gallezot, Nabeel Nabulsi, David Matuskey, Gerard Sanacora, Richard E Carson and 2 more

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2023. 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
2.8field-weighted citation impact, top 8% 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, 21 citations in OpenAlex.

  1. Pooled it
  2. Trajectories of late-life depression: insights from molecular imaging.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  3. Article
  4. In vivo evidence for metabotropic glutamate receptor 5 dysregulation in chronic pain.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  5. Review
  6. Biomarkers of bipolar disorder in omics and neuroimaging.Journal of pharmaceutical analysis · 2025
    Review
  7. Challenges and rewards of in vivo synaptic density imaging, and its application to the study of depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  8. Article
  9. Article
  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

12 authors at 1 institution in 1 country.

Sophie E HolmesDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut.
Ruth H AschDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut.
Margaret T DavisDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut; Department of Psychology, Yale University, New Haven, Connecticut.
Nicole DellaGioiaDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut.
Neha PashankarDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut.
Jean-Dominique GallezotDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut.
Nabeel NabulsiDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut.
David MatuskeyDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut.
Gerard SanacoraDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut.
Richard E CarsonDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut.
Hilary P BlumbergDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut; Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut; Child Study Center, Yale School of Medicine, New Haven, Connecticut.
Irina EsterlisDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut; Child Study Center, Yale School of Medicine, New Haven, Connecticut; Clinical Neurosciences Division, U.S. Department of Veteran Affairs National Center for Posttraumatic Stress Disorder, VA Connecticut Healthcare System, West Haven, Connecticut. Electronic address: irina.esterlis@yale.edu.
Yale University · 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
RESEARCH TRAINING - BIOLOGICAL SCIENCEST32MH014276 · NIMH · YALE UNIVERSITY · PI Marina R Picciotto · 1985 to 2026
$7.2M
In vivo imaging of a neural marker of suicidal behavior in Bipolar DisorderR01MH116657 · NIMH · YALE UNIVERSITY · PI ESTERLIS, IRINA · 2019 to 2024
$4.0M
PET-fMRI Study of Glutamate and Frontal Function in Bi- and Uni-polar DepressionR01MH104459 · NIMH · YALE UNIVERSITY · PI ESTERLIS, IRINA · 2015 to 2019
$3.6M
Dysregulation in mGluR5 as a marker of BPD and suicide related endophenotypesK08MH117351 · NIMH · YALE UNIVERSITY · PI DAVIS, MARGARET TAYLOR · 2018 to 2022
$983k
Role of Beta2-nAChR in Bipolar DisorderK01MH092681 · NIMH · YALE UNIVERSITY · PI ESTERLIS, IRINA · 2011 to 2015
$850k
Using multimodal imaging and the RDoC framework to predict risk factors for suicide attemptR03MH118609 · NIMH · YALE UNIVERSITY · PI HOLMES, SOPHIE · 2019 to 2020
$168k
NCATS NIH HHS UL1 TR001863NIMH NIH HHS K01 MH092681NIMH NIH HHS K08 MH117351NIMH NIH HHS R01 MH104459NIMH NIH HHS R01 MH116657NIMH NIH HHS R03 MH118609NIMH NIH HHS T32 MH014276
6 · The paper itself

Abstract

backgroundUnderstanding the neurobiology underlying bipolar disorder (BD) versus major depressive disorder (MDD) is crucial for accurate diagnosis and for driving the discovery of novel treatments. A promising target is the metabotropic glutamate receptor 5 (mGluR5), a modulator of glutamate transmission associated with synaptic plasticity. We measured mGluR5 availability in individuals with MDD and BD for the first time using positron emission tomography.

methodsIndividuals with BD (n = 17 depressed; n = 10 euthymic) or MDD (n = 17) and healthy control (HC) individuals (n = 18) underwent imaging with [

resultsPrefrontal cortex mGluR5 availability was significantly different across groups (F

conclusionsThis work suggests that mGluR5 could be helpful in distinguishing BD and MDD as a possible treatment target for depressive symptoms in MDD and for cognitive alterations in both disorders. Further work is needed to confirm differentiating roles for mGluR5 in BD and MDD and to probe modulation of mGluR5 as a preventive/treatment strategy.

Indexed as

Bipolar DisorderMajor Depressive DisorderHumansMagnetic Resonance ImagingPositron-Emission TomographyPrefrontal CortexReceptor, Metabotropic Glutamate 5Receptor, Metabotropic Glutamate 5Bipolar disorderDepressionGlutamateImagingmGluR5PET

Identifiers

PMID36764853
PMCPMC10164841
OpenAlexW4308515137

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Registered trials

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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.