Evidence map›Paper›PMID 24091486›Full record

ReviewNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Postmortem brain: an underutilized substrate for studying severe mental illness.

Robert E McCullumsmith, John H Hammond, Dan Shan, James H Meador-Woodruff

Erratum issuedAbstract readReview
In one paragraph

Review 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. An erratum has been issued. Cited by 64 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

64 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Robert E McCullumsmithDepartment of Psychiatry, University of Cincinnati, Cincinnati, OH, USA.
John H Hammond
Dan Shan
James H Meador-Woodruff

Funding

Subcellular Glutamate Receptor Defects in SchizophreniaR01MH053327 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MEADOR-WOODRUFF, JAMES H · 1995 to 2015
$5.8M
Defects of subcellular glutamate transporter localization in schizophreniaR01MH094445 · NIMH · UNIVERSITY OF CINCINNATI · PI MCCULLUMSMITH, ROBERT E · 2011 to 2015
$1.7M
Neuron Subtype and Circuit Specific Patterns of Gene Expression in SchizophreniaRC1MH088752 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MEADOR-WOODRUFF, JAMES H · 2009 to 2010
$1.0M
Glutamate Transporter Expression in SchizophreniaK08MH074016 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MCCULLUMSMITH, ROBERT E · 2006 to 2010
$872k
NIMH NIH HHS K08 MH074016NIMH NIH HHS MH074016NIMH NIH HHS MH094445NIMH NIH HHS MH53327NIMH NIH HHS MH88752NIMH NIH HHS R01 MH053327NIMH NIH HHS R01 MH094445NIMH NIH HHS RC1 MH088752
6 · The paper itself

Abstract

We propose that postmortem tissue is an underutilized substrate that may be used to translate genetic and/or preclinical studies, particularly for neuropsychiatric illnesses with complex etiologies. Postmortem brain tissues from subjects with schizophrenia have been extensively studied, and thus serve as a useful vehicle for illustrating the challenges associated with this biological substrate. Schizophrenia is likely caused by a combination of genetic risk and environmental factors that combine to create a disease phenotype that is typically not apparent until late adolescence. The complexity of this illness creates challenges for hypothesis testing aimed at understanding the pathophysiology of the illness, as postmortem brain tissues collected from individuals with schizophrenia reflect neuroplastic changes from a lifetime of severe mental illness, as well as treatment with antipsychotic medications. While there are significant challenges with studying postmortem brain, such as the postmortem interval, it confers a translational element that is difficult to recapitulate in animal models. On the other hand, data derived from animal models typically provide specific mechanistic and behavioral measures that cannot be generated using human subjects. Convergence of these two approaches has led to important insights for understanding molecular deficits and their causes in this illness. In this review, we discuss the problem of schizophrenia, review the common challenges related to postmortem studies, discuss the application of biochemical approaches to this substrate, and present examples of postmortem schizophrenia studies that illustrate the role of the postmortem approach for generating important new leads for understanding the pathophysiology of severe mental illness.

Indexed as

AnimalsAutopsyBrainDisease Models, AnimalHumansModels, NeurologicalSchizophrenia

Identifiers

PMID24091486
PMCPMC3857666

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.