Evidence map›Paper›PMID 29202778›Full record

ArticleJournal of neuroinflammation2017

Regulator of oligodendrocyte maturation, miR-219, a potential biomarker for MS.

Ilona B Bruinsma, Marie van Dijk, Claire Bridel, Timothy van de Lisdonk, Sanne Q Haverkort, Tessel F Runia, Lawrence Steinman, Rogier Q Hintzen, Joep Killestein, Marcel M Verbeek and 2 more

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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

30 citing papers in PubMed.

  1. Review
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  8. Article
  9. Review
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  11. Article
  12. miRNA Signature in CSF From Patients With Primary Progressive Multiple Sclerosis.Neurology(R) neuroimmunology & neuroinflammation · 2023
    Article
  13. Remyelination in multiple sclerosis from the miRNA perspective.Frontiers in molecular neuroscience · 2023
    Review
  14. Article
  15. An Update on Diagnostic Laboratory Biomarkers for Multiple Sclerosis.Current neurology and neuroscience reports · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

12 authors.

Ilona B BruinsmaDepartment of Neurology, Donders Institute for Brain Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
Marie van DijkMolecular Biology Laboratory, Department of Clinical Chemistry, VU University Medical Center, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0003-1461-3441
Claire BridelNeurochemistry Laboratory and Biobank, Department of Clinical Chemistry, Amsterdam Neuroscience, VU University Medical Center, Amsterdam, the Netherlands.
Timothy van de LisdonkDepartment of Laboratory Medicine, Radboud University Medical Center, Nijmegen, the Netherlands.
Sanne Q HaverkortNeurochemistry Laboratory and Biobank, Department of Clinical Chemistry, Amsterdam Neuroscience, VU University Medical Center, Amsterdam, the Netherlands.
Tessel F RuniaDepartment of Neurology and Department of Immunology, Erasmus MC, Rotterdam, the Netherlands.
Lawrence SteinmanDepartment of Neurological Sciences and Neurology, Stanford University, Stanford, CA, USA.
Rogier Q HintzenDepartment of Neurology and Department of Immunology, Erasmus MC, Rotterdam, the Netherlands.
Joep KillesteinDepartment of Neurology, Amsterdam Neuroscience, VUmc MS Center Amsterdam, VU University Medical Center, Amsterdam, the Netherlands.
Marcel M VerbeekDepartment of Neurology, Donders Institute for Brain Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
Charlotte E TeunissenNeurochemistry Laboratory and Biobank, Department of Clinical Chemistry, Amsterdam Neuroscience, VU University Medical Center, Amsterdam, the Netherlands.
Brigit A de JongDepartment of Neurology, Donders Institute for Brain Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands. b.dejong@vumc.nl.

Funding

Stichting MS Research (NL) 07-610 MS
6 · The paper itself

Abstract

backgroundMultiple sclerosis (MS) is a demyelinating and degenerative disease of the central nervous system. Normally, demyelination is followed by remyelination, which requires repopulation of a demyelinated area by oligodendrocyte precursor cells. Although large numbers of precursor cells are present in MS lesions, remyelination often fails, in part by the inability of precursor cells to differentiate into mature myelin-forming cells. In mouse and rat, miR-219 is required for this differentiation. Previously, we identified decreased miR-219 expression in tissue of MS patients compared to controls. Cell-free miRNAs have been detected in many different body fluids including cerebrospinal fluid (CSF) and may reflect disease processes going on in the central nervous system. This prompted us to investigate the biomarker performance of CSF miR-219 for MS diagnosis.

methodsQuantitative PCR was performed measuring miR-219 levels in CSF of MS patients and controls in three independent cohorts.

resultsAll three cohorts of MS patients and controls revealed that absence of miR-219 detection in CSF is consistently associated with MS.

conclusionsWe have been able to identify and validate absence of miR-219 detection in CSF of MS patients compared to controls, suggesting that it may emerge as a candidate biomarker for MS diagnosis.

Indexed as

AdultBiomarkersFemaleHumansMaleMicroRNAsMiddle AgedMultiple SclerosisBiomarkersMicroRNAsMIRN219 microRNA, humanBiomarkersCerebrospinal fluidmiR-150miR-219miRNAMultiple sclerosis

Identifiers

PMID29202778
PMCPMC5716023

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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.