Evidence map›Paper›PMID 40976818›Full record

ArticleNeurology and therapy2025

Neurofilament Light Chain Levels as Diagnostic and Prognostic Biomarkers in Guillain-Barré Syndrome: An Updated Systematic Review and Meta-Analysis.

Giovanni Siconolfi, Francesca Vitali, Maria Ausilia Sciarrone, Valeria Guglielmino, Guido Primiano, Marco Luigetti

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Article in Neurology and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Giovanni SiconolfiDepartment of Neuroscience, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Francesca VitaliDepartment of Neuroscience, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Maria Ausilia SciarroneDepartment of Neuroscience, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Valeria GuglielminoDepartment of Neuroscience, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Guido PrimianoDepartment of Neuroscience, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Marco LuigettiDepartment of Neuroscience, Catholic University of the Sacred Heart, 00168, Rome, Italy. mluigetti@gmail.com.ORCID http://orcid.org/0000-0001-7539-505X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGuillain-Barré syndrome (GBS) is an acute immune-mediated disorder of the peripheral nervous system, marked by rapid onset of neurological symptoms. Despite progress in understanding the etiology and improving clinical management, no validated biomarkers are currently available to predict disease severity or treatment response during the acute phase. This meta-analysis aims to evaluate the role of serum neurofilament light chain (NfL) as a biomarker of acute disease activity and prognostic outcomes in GBS.

methodsA systematic review and meta-analysis was conducted using PubMed, Scopus, and Cochrane Library databases to identify studies assessing NfL levels in patients with GBS. In addition, we included data from our own cohort of patients with GBS-whose NfL levels were measured at disease onset-and from healthy controls. The primary outcome was the difference in NfL levels-both in serum and cerebrospinal fluid (CSF)-between patients with GBS and controls. Secondary outcomes included the correlations between acute-phase NfL levels, clinical severity at admission as measured by the Guillain-Barré Disability Scale (GBDS) or the Hughes Functional Scale (HFS), and long-term outcomes such as the inability to walk or run 1 year after disease onset.

resultsIn this meta-analysis of nine studies, which also included data from our cohort, serum NfL levels were significantly higher in patients with GBS compared with controls (mean difference 143.17 pg/mL, 95% CI 67.7-218.6; p < 0.01; I

conclusionSerum NfL is a promising biomarker for early diagnosis and prognosis in GBS and may support risk stratification at hospital admission.

Indexed as

Acute polyneuropathiesBiomarkerGuillain–Barré syndromeNeurofilament light chainPrognosis

Identifiers

PMID40976818
PMCPMC12623590

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