Evidence map›Paper›PMID 34880402›Full record

ArticleScientific reports2021

Osteopontin levels are associated with late-time lower regional brain volumes in multiple sclerosis.

Gergely Orsi, Zsofia Hayden, Tamas Cseh, Timea Berki, Zsolt Illes

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. 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
1.0field-weighted citation impact, top 25% 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, 16 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

5 authors at 3 institutions in 2 countries.

Gergely OrsiMTA-PTE Clinical Neuroscience MR Research Group, Eötvös Loránd Research Network (ELKH), Ret str. 2, 7623, Pecs, Hungary. gergo.orsi@gmail.com.
Zsofia HaydenDepartment of Immunology and Biotechnology, Medical School, University of Pecs, Pecs, Hungary.
Tamas CsehDepartment of Neurology, Medical School, University of Pecs, Pecs, Hungary.
Timea BerkiDepartment of Immunology and Biotechnology, Medical School, University of Pecs, Pecs, Hungary.
Zsolt IllesDepartment of Neurology, Medical School, University of Pecs, Pecs, Hungary.
University of Pecs · HUHungarian Research NetworkOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteopontin (OPN) is a proinflammatory marker produced by systemic immune and central nervous system (CNS) resident cells. We examined, if the level of OPN in the cerebrospinal fluid (CSF) and blood is associated with late-time regional brain volumes and white matter (WM) lesion load in MS. Concentrations of OPN in blood and CSF were related to MRI findings 10.1 ± 2.0 years later in 46 patients with MS. OPN concentration was measured by ELISA, while regional brain volumes and lesion load was assessed by magnetic resonance imaging (MRI) using 3D MPRAGE sequence and automated MR volumetry. OPN measured in the CSF was associated with several regional brain volumes and WM lesion load measured 10.1 ± 2.0 years later. CSF OPN concentration correlated with long-term enlargement of lateral- and inferior lateral ventricles and the elevation of gross CSF volume, in conjunction with the reduction of several cortical/subcortical gray matter and WM volumes. Serum OPN showed no long-term association with regional brain volumes. OPN measured from the CSF but not from the serum was associated with lower regional brain volumes measured a decade later, indicating the primary role of inflammation within the CNS in developing long-term brain related alterations.

Indexed as

AdultAgedBrainFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedMultiple SclerosisOsteopontinYoung AdultOsteopontin

Identifiers

PMID34880402
PMCPMC8654976
OpenAlexW4200356175

What OpenQuestion holds

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LicenceCC BY
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.