Evidence map›Paper›PMID 27013967›Full record

ArticleFrontiers in cellular neuroscience2016

Serum S100B Protein is Specifically Related to White Matter Changes in Schizophrenia.

Berko Milleit, Stefan Smesny, Matthias Rothermundt, Christoph Preul, Matthias L Schroeter, Christof von Eiff, Gerald Ponath, Christine Milleit, Heinrich Sauer, Christian Gaser

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

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  8. Schizophrenia and Alarmins.Medicina (Kaunas, Lithuania) · 2022
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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

10 authors at 5 institutions in 2 countries.

Berko MilleitDepartment of Psychiatry, Jena University HospitalJena, Germany; St. Joseph-KrankenhausDessau-Roßlau, Germany.
Stefan SmesnyDepartment of Psychiatry, Jena University Hospital Jena, Germany.
Matthias RothermundtDepartment of Psychiatry, University of MuensterMuenster, Germany; Department of Psychiatry, St. Rochus HospitalTelgte, Germany.
Christoph PreulDepartment of Neurology, Jena University Hospital Jena, Germany.
Matthias L SchroeterMax Planck Institute for Human Cognitive and Brain Sciences and Clinic for Cognitive Neurology Leipzig, Germany.
Christof von EiffInstitute of Medical Microbiology, University of Muenster Muenster, Germany.
Gerald PonathDepartment of Psychiatry, University of MuensterMuenster, Germany; Department of Neurology, School of Medicine, Yale UniversityNew Haven, CT, USA.
Christine MilleitDepartment of Psychiatry, Jena University HospitalJena, Germany; Department of Psychiatry, Sophien- und Hufeland-KlinikumWeimar, Germany.
Heinrich SauerDepartment of Psychiatry, Jena University Hospital Jena, Germany.
Christian GaserDepartment of Psychiatry, Jena University HospitalJena, Germany; Department of Neurology, Jena University HospitalJena, Germany.
Jena University Hospital · DEUniversity of Münster · DEMax Planck Institute for Human Cognitive and Brain Sciences · DESophien-und Hufeland Klinikum · DESt. Joseph-Krankenhaus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSchizophrenia can be conceptualized as a form of dysconnectivity between brain regions.To investigate the neurobiological foundation of dysconnectivity, one approach is to analyze white matter structures, such as the pathology of fiber tracks. S100B is considered a marker protein for glial cells, in particular oligodendrocytes and astroglia, that passes the blood brain barrier and is detectable in peripheral blood. Earlier Studies have consistently reported increased S100B levels in schizophrenia. In this study, we aim to investigate associations between S100B and structural white matter abnormalities.

methodsWe analyzed data of 17 unmedicated schizophrenic patients (first and recurrent episode) and 22 controls. We used voxel based morphometry (VBM) to detect group differences of white matter structures as obtained from T1-weighted MR-images and considered S100B serum levels as a regressor in an age-corrected interaction analysis.

resultsS100B was increased in both patient subgroups. Using VBM, we found clusters indicating significant differences of the association between S100B concentration and white matter. Involved anatomical structures are the posterior cingulate bundle and temporal white matter structures assigned to the superior longitudinal fasciculus.

conclusionsS100B-associated alterations of white matter are shown to be existent already at time of first manifestation of psychosis and are distinct from findings in recurrent episode patients. This suggests involvement of S100B in an ongoing and dynamic process associated with structural brain changes in schizophrenia. However, it remains elusive whether increased S100B serum concentrations in psychotic patients represent a protective response to a continuous pathogenic process or if elevated S100B levels are actively involved in promoting structural brain damage.

Indexed as

first episode psychosisS100BschizophreniaVBMvoxel based morphometrywhite matter

Identifiers

PMID27013967
PMCPMC4782018
OpenAlexW2297007627

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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.