Evidence map›Paper›PMID 40316442›Full record

Trial reportJournal of neurology, neurosurgery, and psychiatry2025

Neurofilament light chain improves clinical prognostic models for Guillain-Barré syndrome.

Robin C M Thomma, Linda W G Luijten, Sander J van Tilburg, Eveline J A Wiegers, Charlotte E Teunissen, Lisa Vermunt, Pieter A van Doorn, Ruth Huizinga, Bart C Jacobs

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of neurology, neurosurgery, and psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

9 authors.

Robin C M ThommaDepartment of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-5584-2457
Linda W G LuijtenDepartment of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Sander J van TilburgDepartment of Immunology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Eveline J A WiegersDepartment of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0003-1768-7550
Charlotte E TeunissenNeurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam Neuroscience, Amsterdam University Medical Centres, Amsterdam, The Netherlands.
Lisa VermuntNeurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam Neuroscience, Amsterdam University Medical Centres, Amsterdam, The Netherlands.
Pieter A van DoornDepartment of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Ruth HuizingaDepartment of Immunology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-9563-4860
Bart C JacobsDepartment of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands b.jacobs@erasmusmc.nl.ORCID http://orcid.org/0000-0002-8985-2458

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral prognostic models predict clinical outcomes in Guillain-Barré syndrome (GBS). Recently, neurofilament light chain (NfL) has emerged as a prognostic biomarker. We investigated the added prognostic value of NfL in serum (sNfL) and cerebrospinal fluid (cNfL) to models based on clinical factors predicting respiratory failure and inability to walk in GBS.

methodsWe included patients from a randomised placebo-controlled trial (second intravenous immunoglobulin dose in GBS). Serum was acquired at entry and week 1, 2, 4 and 12 and cerebrospinal fluid at entry. NfL levels were determined on a single molecule array. The additional prognostic value of NfL to the (modified) Erasmus GBS Outcome Score ((m)EGOS) and (modified) Erasmus GBS Respiratory Insufficiency Score was evaluated using logistic regression analyses.

resultsIn total, 293 patients were included (74 (25%) mechanically ventilated, 38/275 (13%) unable to walk at 26 weeks). Higher sNfL at entry, week 1 and week 2 and cNfL at entry were associated with inability to walk at 4 and 26 weeks. Neither sNfL nor cNfL levels at entry were associated with respiratory failure. The EGOS and mEGOS improved after adding NfL (∆C-statistic range: 0.01-0.11), especially the models predicting outcome at 26 weeks. A new model predicting inability to walk at 26 weeks consisting of sNfL at entry, GBS disability score at entry and Medical Research Council sum score at week 2 performed best (C-statistic: 0.88 (95% CI 0.83 to 0.94)).

conclusionsAddition of NfL may improve clinical prognostic models for the prediction of inability to walk, but not of respiratory failure. TRIAL REGISTRATION NUMBER: NTR2224/NL2107.

Indexed as

Guillain-Barre SyndromeNeurofilament ProteinsAdultAgedBiomarkersFemaleHumansImmunoglobulins, IntravenousMaleMiddle AgedPrognosisRespiration, ArtificialRespiratory InsufficiencyBiomarkersImmunoglobulins, Intravenousneurofilament protein LNeurofilament ProteinsGUILLAIN-BARRE SYNDROMEPatient Outcome AssessmentPrognosis

Identifiers

PMID40316442
PMCPMC12573411

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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.