Evidence map›Paper›PMID 39494701›Full record

ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2024

Serum neurofilament light and glial fibrillary acidic protein levels are not associated with wearing-off symptoms in natalizumab-treated multiple sclerosis patients.

Alyssa A Toorop, Mark Hj Wessels, Lynn Boonkamp, Liza My Gelissen, E Hoitsma, Esther Mpe Zeinstra, Luuk C van Rooij, Caspar Ep van Munster, Anke Vennegoor, Jop P Mostert and 22 more

Abstract read
In one paragraph

Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

32 authors.

Alyssa A TooropDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-7196-9826
Mark Hj WesselsDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-2324-0499
Lynn BoonkampNeurochemistry Laboratory, Department of Laboratory Medicine, Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam, The Netherlands.
Liza My GelissenDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
E HoitsmaDepartment of Neurology, MS Center Alrijne Hospital, Leiden, The Netherlands.
Esther Mpe ZeinstraDepartment of Neurology, Isala, Meppel, The Netherlands.
Luuk C van RooijDepartment of Neurology, Maasstad Hospital, Rotterdam, The Netherlands.
Caspar Ep van MunsterDepartment of Neurology, Amphia, Breda, The Netherlands.
Anke VennegoorDepartment of Neurology, Flevoziekenhuis, Almere, The Netherlands.
Jop P MostertDepartment of Neurology, Rijnstate Hospital, Arnhem, The Netherlands.
Beatrijs Ha WokkeDepartment of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-2616-8464
Nynke F KalkersDepartment of Neurology, OLVG, Amsterdam, The Netherlands.
Erwin Lj HoogervorstDepartment of Neurology, St. Antonius Ziekenhuis, Utrecht, The Netherlands.
Jeroen Jj van EijkDepartment of Neurology, Jeroen Bosch Ziekenhuis/Hospital, 's-Hertogenbosch, The Netherlands.
Christiaan M RoosendaalDepartment of Neurology, Slingeland Hospital, Doetinchem, The Netherlands.
Jolijn J KragtDepartment of Neurology, Reinier de Graaf Hospital, Delft, The Netherlands.
Marijke EurelingsDepartment of Neurology, Spaarne Gasthuis, Haarlem, The Netherlands.
Jessie van GenugtenDepartment of Neurology, Ziekenhuisgroep Twente, Almelo, The Netherlands.
Jessica NielsenDepartment of Neurology, Ommelander Ziekenhuis, Scheemda, The Netherlands.
Lgf SinnigeDepartment of Neurology, Medisch Centrum Leeuwarden, Leeuwarden, The Netherlands.
Mark E KloosterzielDepartment of Neurology, Wilhelmina Hospital, Assen, The Netherlands.
Edo Pj ArnoldusDepartment of Neurology, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.
Gert W van DijkDepartment of Neurology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
Willem H BouvyDepartment of Neurology, Diakonessenhuis Hospital, Utrecht, The Netherlands.
Eva Mm StrijbisDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0001-6705-5864
Bob W van OostenDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Brigit A de JongDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Bernard Mj UitdehaagDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Theo RispensSanquin Diagnostic Services, Amsterdam, the Netherlands.ORCID 0000-0001-9600-1312
Joep KillesteinDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Zoé LE van KempenDepartment of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0001-9557-5381
Charlotte E TeunissenNeurochemistry Laboratory, Department of Laboratory Medicine, Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiomarkers of neuronal and axonal damage (serum neurofilament light (sNfL) and serum glial fibrillary acidic protein (sGFAP)) may provide insight into the aetiology of natalizumab wearing-off symptoms (WoSs).

objectivesWe investigated the longitudinal association between and predictive value of sNfL and sGFAP and the occurrence of WoS in MS patients treated with natalizumab.

methodsWe performed longitudinal measurements of sNfL and sGFAP in NEXT-MS trial participants who completed a questionnaire about WoS.

resultsA total of 364 participants were included. In total, 55.5% presented with WoS and 44.5% without WoS during natalizumab treatment. Longitudinal analyses showed no association between sNfL and sGFAP levels and WoS at any timepoint. Biomarker levels at baseline did not predict first-time WoS occurrence.

conclusionAcute and chronic neuronal and axonal damage are most likely not the underlying cause of WoS.

Indexed as

BiomarkersGlial Fibrillary Acidic ProteinImmunologic FactorsNatalizumabNeurofilament ProteinsAdultFemaleHumansLongitudinal StudiesMaleMiddle AgedMultiple SclerosisMultiple Sclerosis, Relapsing-RemittingBiomarkersGFAP protein, humanGlial Fibrillary Acidic ProteinImmunologic FactorsNatalizumabneurofilament protein LNeurofilament ProteinsbiomarkersMultiple sclerosisnatalizumabtreatment response

Identifiers

PMID39494701
PMCPMC11568651

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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.