Evidence map›Paper›PMID 36695545›Full record

Observational studyBiomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia2023

Cerebrospinal fluid neurofilament light chains and CXCL13 as predictive factors for clinical course of multiple sclerosis.

Pavel Hradilek, Kamila Zondra Revendova, Jana Horakova, Radovan Bunganic, Ondrej Pelisek, David Zeman, Pavla Hanzlikova, Pavlina Kusnierova

Open access · goldAbstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 6 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

8 authors at 4 institutions in 1 country.

Pavel HradilekDepartment of Clinical Neurosciences, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
Kamila Zondra RevendovaDepartment of Clinical Neurosciences, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
Jana HorakovaDepartment of Neurology, University Hospital Ostrava, Ostrava, Czech Republic.
Radovan BunganicDepartment of Clinical Neurosciences, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
Ondrej PelisekFaculty of Medicine, Masaryk University, Brno, Czech Republic.
David ZemanDepartment of Laboratory Medicine, University Hospital Brno, Brno, Czech Republic.
Pavla HanzlikovaDepartment of Imaging Methods, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
Pavlina KusnierovaDepartment of Clinical Biochemistry, Institute of Laboratory Medicine, University Hospital Ostrava, Ostrava, Czech Republic.
University Hospital Ostrava · CZUniversity of Ostrava · CZMasaryk University · CZUniversity Hospital Brno · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe aim of this study was to identify whether NfL and CXCL13 cerebrospinal fluid (CSF) concentrations at diagnostic lumbar puncture can predict the course of multiple sclerosis (MS) in terms of relapses, higher expanded disability status scale (EDSS) and magnetic resonance imaging (MRI) activity.

methodsWe conducted a single-centre prospective observational cohort study at the MS center, University Hospital Ostrava, Czech Republic. CSF NfL (cNfL) and CXCL13 concentrations were examined (ELISA method) in patients with clinically isolated syndrome (CIS) and relapsing-remitting MS (RRMS) at the time of diagnostic lumbar puncture.

resultsA total of 44 patients with CIS or early RRMS were enrolled, 31 (70.5%) of whom were women. The median age at the time of CSF sampling was 31.21 years (IQR 25.43-39.32), and the follow-up period was 54.6 months (IQR 44.03-59.48). In the simple and multiple logistic regression models, CXCL13 levels did not predict relapses, MRI activity or EDSS > 2.5. Similarly, cNfL concentrations did not predict relapses or MRI activity in either model. In the multiple regression, higher cNfL levels were associated with reaching EDSS > 2.5 (odds ratio [OR] 1.002, 95% confidence interval [CI] 1.000 to 1.003).

conclusionsOur data did not confirm cNfL and/or CXCL13 CSF levels were predictive factors for disease activity such as relapses and MRI activity at the time of diagnostic lumbar puncture in patients with RRMS. While cNfL CSF levels predicted higher disability only after adjustment for other known risk factors, elevated CSF CXCL13 did not predict higher disability at all.

Indexed as

Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingAdultBiomarkersChemokine CXCL13Disease ProgressionFemaleHumansIntermediate FilamentsMaleProspective StudiesRecurrenceBiomarkersChemokine CXCL13CXCL13 protein, humanbiomarkersclinical courseCXCL13multiple sclerosisneurofilament light chain

Identifiers

PMID36695545
OpenAlexW4317935514

What OpenQuestion holds

Textmetadata
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.