Evidence map›Paper›PMID 26686292›Full record

ArticleJournal of chemical neuroanatomy2016

Reduced GABA neuron density in auditory cerebral cortex of subjects with major depressive disorder.

John F Smiley, Troy A Hackett, Cynthia Bleiwas, Eva Petkova, Aleksandar Stankov, J John Mann, Gorazd Rosoklija, Andrew J Dwork

Abstract read
In one paragraph

Article in Journal of chemical neuroanatomy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 5 pooled it
1.3field-weighted citation impact, top 23% 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, 5 syntheses or guidelines pooled it, 34 citations in OpenAlex.

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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

8 authors at 5 institutions in 2 countries.

John F SmileyProgram in Cognitive Neuroscience and Schizophrenia, Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, USA; Department of Child and Adolescent Psychiatry, New York University Langone Medical Center, New York, NY, USA. Electronic address: smiley@nki.rfmh.org.
Troy A HackettDepartment of Psychology, Vanderbilt University School of Medicine, Nashville, TN, USA.
Cynthia BleiwasProgram in Cognitive Neuroscience and Schizophrenia, Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, USA.
Eva PetkovaProgram in Cognitive Neuroscience and Schizophrenia, Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, USA; Department of Child and Adolescent Psychiatry, New York University Langone Medical Center, New York, NY, USA.
Aleksandar StankovInstitute for Forensic Medicine, School of Medicine, Skopje, Macedonia.
J John MannDivision of Molecular Imaging and Neuropathology, New York State Psychiatric Institute and Columbia University, New York, NY, USA; Department of Neuroscience, New York State Psychiatric Institute, New York, NY, USA.
Gorazd RosoklijaDivision of Molecular Imaging and Neuropathology, New York State Psychiatric Institute and Columbia University, New York, NY, USA; Department of Neuroscience, New York State Psychiatric Institute, New York, NY, USA; Macedonian Academy of Sciences and Arts, Skopje, Macedonia.
Andrew J DworkDivision of Molecular Imaging and Neuropathology, New York State Psychiatric Institute and Columbia University, New York, NY, USA; Department of Neuroscience, New York State Psychiatric Institute, New York, NY, USA; Macedonian Academy of Sciences and Arts, Skopje, Macedonia.
Columbia University · USNathan Kline Institute for Psychiatric Research · USNew York Psychoanalytic Society and Institute · USNYU Langone Health · USVanderbilt University · US

Funding

The Conte Center for Schizophrenia ResearchP50MH086385 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI JAVITT, DANIEL C. · 2009 to 2013
$10.7M
Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DYKENS, ELISABETH MAY · 2015 to 2019
$7.1M
Discovery, characterization and preclinical development of pro-neurogenic drugsR01MH087986 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI MCKNIGHT, STEVEN L, PIEPER, ANDREW A · 2009 to 2013
$6.2M
Golgi Studies of SchizophreniaR01MH064168 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI DWORK, ANDREW J · 2001 to 2013
$4.3M
Myelin Pathology in SchizophreniaR01MH060877 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI DWORK, ANDREW J · 1999 to 2011
$2.4M
Cortical interneuron number and expression profile in schizophreniaR21MH085208 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI SMILEY, JOHN F · 2009 to 2010
$435k
GPU-Accelerated Parallel Computer for Drug Discovery ApplicationsS10OD020154 · OD · VANDERBILT UNIVERSITY · PI SMITH, JARROD ANSON · 2015 to 2015
$225k
NICHD NIH HHS U54 HD083211NIMH NIH HHS P50 MH086385NIMH NIH HHS R01 MH060877NIMH NIH HHS R01 MH064168NIMH NIH HHS R01 MH087986NIMH NIH HHS R21 MH085208
6 · The paper itself

Abstract

Although major depressive disorder (MDD) and schizophrenia (SZ) are closely associated with disrupted functions in frontal and limbic areas of cerebral cortex, cellular pathology has also been found in other brain areas, including primary sensory cortex. Auditory cortex is of particular interest, given the prominence of auditory hallucinations in SZ, and sensory deficits in MDD. We used stereological sampling methods in auditory cortex to look for cellular differences between MDD, SZ and non-psychiatric subjects. Additionally, as all of our MDD subjects died of suicide, we evaluated the association of suicide with our measurements by selecting a SZ sample that was divided between suicide and non-suicide subjects. Measurements were done in primary auditory cortex (area A1) and auditory association cortex (area Tpt), two areas with distinct roles in sensory processing and obvious differences in neuron density and size. In MDD, densities of GABAergic interneurons immunolabeled for calretinin (CR) and calbindin (CB) were 23-29% lower than non-psychiatric controls in both areas. Parvalbumin (PV) interneurons (counted only in area Tpt) showed a nominally smaller (16%) reduction that was not statistically significant. Total neuron and glia densities measured in Nissl stained sections did not show corresponding reductions. Analysis of suicide in the SZ sample indicated that reduced CR cell density was associated with suicide, whereas the densities of CB and other cells were not. Our results are consistent with previous studies in MDD that found altered GABA-associated markers throughout the cerebral cortex including primary sensory areas.

Indexed as

Human postmortemInterneuronMajor depressionPsychiatricSchizophreniaSensory cortexStereologySuicide

Identifiers

PMID26686292
PMCPMC4903945
OpenAlexW2204831719

What OpenQuestion holds

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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.