Evidence map›Paper›PMID 24078172›Full record

ArticleSchizophrenia bulletin2014

ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies.

Carl Christoph Schultz, Igor Nenadic, Brien Riley, Vladimir I Vladimirov, Gerd Wagner, Kathrin Koch, Claudia Schachtzabel, Thomas W Mühleisen, Buket Basmanav, Markus M Nöthen and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Schizophrenia bulletin, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

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  6. Effect of rs1344706 in theNeuroImage. Clinical · 2018
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 8 institutions in 4 countries.

Carl Christoph Schultz*To whom correspondence should be addressed; Department of Psychiatry and Psychotherapy, Jena University Hospital, Philosophenweg 3, 07740 Jena, Germany; tel: +49-3641-9-35665, fax: +49-3641-9-35444, e-mail: christoph.schultz@med.uni-jena.de.
Igor Nenadic
Brien Riley
Vladimir I Vladimirov
Gerd Wagner
Kathrin Koch
Claudia Schachtzabel
Thomas W Mühleisen
Buket Basmanav
Markus M Nöthen
Thomas Deufel
Michael Kiehntopf
Marcella Rietschel
Jürgen R Reichenbach
Sven Cichon
Ralf G M Schlösser
Heinrich Sauer
Jena University Hospital · DECentral Institute of Mental Health · DEDepartment of Biomedicine Basel · CHForschungszentrum Jülich · DEInstitute of Human Genetics · PLKlinikum rechts der Isar · DELife & Brain (Germany) · DEVirginia Commonwealth University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent evidence indicated that the ZNF804A (rs1344706) risk allele A is associated with better cognitive performance in patients with schizophrenia. Moreover, it has been demonstrated that ZNF804A may also be related to relatively intact gray matter volume in patients. To further explore these putatively protective effects, the impact of ZNF804A on cortical thickness and folding was examined in this study. To elucidate potential molecular mechanisms, an allelic-specific gene expression study was also carried out. Magnetic resonance imaging cortical thickness and folding were computed in 55 genotyped patients with schizophrenia and 40 healthy controls. Homozygous risk allele carriers (AA) were compared with AC/CC carriers. ZNF804A gene expression was analyzed in a prefrontal region using postmortem tissue from another cohort of 35 patients. In patients, AA carriers exhibited significantly thicker cortex in prefrontal and temporal regions and less disturbed superior temporal cortical folding, whereas the opposite effect was observed in controls, ie, AA carrier status was associated with thinner cortex and more severe altered cortical folding. Along with this, our expression analysis revealed that the risk allele is associated with lower prefrontal ZNF804A expression in patients, whereas the opposite effect in controls has been observed by prior analyses. In conclusion, our analyses provide convergent support for the hypothesis that the schizophrenia-associated ZNF804A variant mediates protective effects on cortex structure in patients. In particular, the allele-specific expression profile in patients might constitute a molecular mechanism for the observed protective influence of ZNF804A on cortical thickness and folding and potentially other intermediate phenotypes.

Indexed as

AdolescentAdultCase-Control StudiesCerebral CortexCognition DisordersFemaleGene Expression ProfilingGray MatterHeterozygoteHomozygoteHumansKruppel-Like Transcription FactorsMagnetic Resonance ImagingMaleOrgan SizePrefrontal CortexKruppel-Like Transcription FactorsZNF804A protein, humancortical foldingcortical thicknessgene expressionpsychosisrs1344706schizophreniasusceptibility geneZNF804A

Identifiers

PMID24078172
PMCPMC3984519
OpenAlexW2164303355

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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.