Evidence map›Paper›PMID 39562307›Full record

ArticleEuropean journal of neurology2025

Serum neurofilament light chain predicts disease severity in axonal variants of acute immune neuropathies: A retrospective monocentric cohort study.

Ali Maisam Afzali, Milan Vosko, Nya Reinhardt, Iaroslav Zinevych, Vincent Gmeiner, Thomas Korn, Christiane Gasperi, Achim Berthele, Emily Feneberg, Bernhard Hemmer

Abstract read
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Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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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

10 authors.

Ali Maisam AfzaliDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.ORCID 0000-0002-3256-5298
Milan VoskoDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.
Nya ReinhardtDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.
Iaroslav ZinevychDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.
Vincent GmeinerDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.
Thomas KornDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.
Christiane GasperiDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.
Achim BertheleDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.
Emily FenebergDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.
Bernhard HemmerDepartment of Neurology, Technical University of Munich School of Medicine and Health, Munich, Germany.ORCID 0000-0001-5985-6784

Funding

Deutsche Forschungsgemeinschaft EXC 2145 SyNergy - ID 390857198Else Kröner-Fresenius-Stiftung 2021_EKEA.164
6 · The paper itself

Abstract

background and purposeThe purpose was to explore the prognostic utility of neurofilament light chain (NfL) in patients with immune-mediated polyradiculoneuropathies (IMPs).

methodsThis retrospective monocentric study analysed serum and cerebrospinal fluid samples from patients diagnosed with IMP collected prior to treatment initiation. NfL concentrations were correlated with clinical outcomes, including F score and hospitalization duration.

resultsAmongst 115 IMP patients tested, baseline cerebrospinal fluid and serum NfL (sNfL) concentrations were higher in acute inflammatory axonal polyradiculoneuropathy (AIAP) than other IMP variants. In the AIAP cohort, a positive correlation was observed between baseline sNfL concentrations, F score and hospitalization duration. Multivariate linear regression analysis further supported the predictive relationship between elevated baseline sNfL concentrations and clinical outcomes. Using receiver operating characteristic analysis, a cut-off value for sNfL of 351 pg/mL was found to predict an F score >3 in AIAP with a sensitivity of 40% and specificity of 81.8%. AIAP patients with sNfL concentrations above this threshold required longer hospitalization (extended by 15 days). DISCUSSION: Our findings highlight the potential of baseline sNfL as an effective marker for distinguishing between IMP variants and predicting the prognosis of AIAP. Further validation may facilitate translation of sNfL into clinical practice, potentially identifying high-risk patients for tailored treatment approaches.

Indexed as

Neurofilament ProteinsAdultAgedBiomarkersCohort StudiesFemaleGuillain-Barre SyndromeHumansMaleMiddle AgedPrognosisRetrospective StudiesSeverity of Illness IndexBiomarkersneurofilament protein LNeurofilament Proteinsacute axonal immune neuropathyGBSimmune neuropathiesNfL

Identifiers

PMID39562307
PMCPMC11625949

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