Evidence map›Paper›PMID 33890175›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2021

Cortical copper transporter expression in schizophrenia: interactions of risk gene dysbindin-1.

Kirsten E Schoonover, William M Kennedy, Rosalinda C Roberts

Open access · greenAbstract read
In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Genetic polymorphism and neuroanatomical changes in schizophrenia.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Review
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

3 authors at 1 institution in 1 country.

Kirsten E SchoonoverDepartment of Psychology and Behavioral Neuroscience, The University of Alabama at Birmingham, 3811 O'Hara Street BST W1651, Pittsburgh, PA, 15213, USA. Schoonoverke@upmc.edu.ORCID 0000-0002-1960-7887
William M KennedyDepartment of Psychiatry and Behavioral Neurobiology, The University of Alabama at Birmingham, Pittsburgh, USA.
Rosalinda C RobertsDepartment of Psychiatry and Behavioral Neurobiology, The University of Alabama at Birmingham, Pittsburgh, USA.
University of Alabama at Birmingham · US

Funding

Mechanisms of copper dysregulation in schizophreniaR21MH117434 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROBERTS, ROSALINDA C · 2018 to 2019
$400k
Mechanisms of Dysbindin Abnormalities in SchizophreniaF99NS105208 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SCHOONOVER, KIRSTEN · 2017 to 2018
$71k
NIMHD NIH HHS R21117434NIMH NIH HHS R21 MH117434NINDS NIH HHS F99 NS105208NINDS NIH HHS F99NS105208
6 · The paper itself

Abstract

Schizophrenia susceptibility factor dysbindin-1 is associated with cognitive processes. Downregulated dysbindin-1 expression is associated with lower expression of copper transporters ATP7A and CTR1, required for copper transport to the central nervous system. We measured dysbindin-1 isoforms-1A and -1BC, CTR1, and ATP7A via Western blots of the postmortem dorsolateral prefrontal cortex (DLPFC) of schizophrenia subjects (n = 28) and matched controls (n = 14). In addition, we subdivided the schizophrenia group by treatment status and comorbidity of alcohol use disorder (AUD) and assessed the relationships between proteins. Schizophrenia subjects exhibited similar protein levels to that of controls, with no effect of antipsychotic treatment. We observed a shift towards more dysbindin-1A expression in schizophrenia, as revealed by the ratio of dysbindin-1 isoforms. Dysbindin-1A expression was negatively correlated with ATP7A in schizophrenia, with no correlation present in controls. AUD subjects exhibited less dysbindin-1BC and CTR1 than those without AUD. Our results, taken together with previous data, suggest that alterations in dysbindin-1 and copper transporters are brain-region specific. For example, protein levels of ATP7A, dysbindin 1BC, and CTR1 are lower in the substantia nigra in schizophrenia subjects. AUD in the DLPFC was associated with lower protein levels of dysbindin-1 and CTR1. Changes in dysbindin-1 isoform ratio and relationships appear to be prevalent in the disease, potentially impacting symptomology.

Indexed as

Antipsychotic AgentsDysbindinSchizophreniaCopperCopper Transport ProteinsHumansPrefrontal CortexAntipsychotic AgentsCopperCopper Transport ProteinsDTNBP1 protein, humanDysbindinAlcoholATP7ACognitionCopperCTR1Postmortem

Identifiers

PMID33890175
PMCPMC11000637
OpenAlexW3154600832

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.