Evidence map›Paper›PMID 41803257›Full record

ArticleJournal of neurology2026

The predictive value of serum neurofilament light chain in achieving no evidence of disease activity-3 (NEDA-3) status in treatment-naïve patients with multiple sclerosis.

Evangelia Makrina Dimitriadou, Dimitrios Tzanetakos, Aikaterini Theodorou, Alexandra Akrivaki, Dimitrios Papadopoulos, Vasileios Mastorodemos, Aleksandra Maleska, Stefania Alexia Sotirli, Nikolaos Fakas, Christos Stergiou and 7 more

Abstract read
In one paragraph

Article in Journal of neurology, 2026. 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

17 authors.

Evangelia Makrina DimitriadouSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
Dimitrios TzanetakosSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
Aikaterini TheodorouSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
Alexandra AkrivakiSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
Dimitrios PapadopoulosMedical School, European University of Cyprus, Nicosia, Cyprus.
Vasileios MastorodemosNeurology Department, University Hospital of Heraklion, Heraklion, Greece.
Aleksandra MaleskaDepartment of Neurology, University Hospital and University of Basel, Basel, Switzerland.
Stefania Alexia SotirliDepartment of Neurology, Metropolitan General Hospital, Athens, Greece.
Nikolaos FakasDepartment of Neurology, 401 General Military Hospital, 11525, Athens, Greece.
Christos StergiouTzartos NeuroDiagnostics, Athens, Greece.
Dimitrios KitsosSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
Vasileios GiannopapasSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
Christos MoschovosSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
Sotirios GiannopoulosSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
Jens KuhleDepartment of Neurology, University Hospital and University of Basel, Basel, Switzerland.
Georgios TsivgoulisSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece.
John S TzartosSecond Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Rimini 1, 12462, Athens, Greece. jtzartos@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSerum neurofilament light chain (sNfL) has emerged as a biomarker reflecting neuroaxonal damage. The role of sNfL in predicting clinical outcome and guiding therapeutic management in multiple sclerosis (MS) is an ongoing research topic. We sought to evaluate sNfL utility for the prediction of achieving No Evidence of Disease Activity-3 (NEDA-3) among MS patients.

methodsWe conducted a prospective cohort study including MS patients with a single sNfL measurement at first clinical evaluation. Follow-up was performed every 6 months/clinical relapse and included clinical and MRI evaluation. The main outcome was NEDA-3 achievement during follow-up. sNfL levels were measured, using single-molecule-array (SIMOA) assay. sNfL age- and BMI-normalized Z-scores > 1.5 were defined as high. Linear regression analyses were performed to identify predictors of baseline sNfL Z-score and multivariable Cox proportional hazard regression models were used to evaluate predefined outcomes.

resultsWe included 125 patients [age at sNfL measurement:40 ± 12, 30% men, 82% relapsing-remitting and 18% progressive MS]:37 treatment-naïve patients, 88 patients under Disease-Modifying-Treatment (DMT) with 19.1 (Interquartile Range:12.1-24.5) months median follow-up. Prior DMT use [β:-0.93; 95%CI:-1.48- -0.38 p-value:0.001] was negatively associated with baseline sNfL Z-scores. Gadolinium-enhancing lesions were associated with higher sNfL Z-scores [adjusted standardized linear regression coefficient-β:0.68; 95%CI:0.03-1.32; p-value:0.036], contrary to T2-weighted lesion activity (β:0.40; 95%CI:0.17-0.94; p-value:0.232). In treatment-naive patients, high sNfL Z-scores were associated with lower probability of achieving NEDA-3 during follow-up [hazard-ratio:0.35; 95%CI:0.13-0.96; p-value:0.041].

conclusionsThis study demonstrated that gadolinium-enhancing lesions, indicative of active inflammation, are associated with elevated sNfL Z-scores, contrary to T2-weighted lesion-activity and highlights the prognostic value of sNfL in achieving NEDA-3 in treatment-naive patients.

Indexed as

Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingNeurofilament ProteinsAdultBiomarkersCohort StudiesDisease ProgressionFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleMiddle AgedPredictive Value of TestsProspective StudiesBiomarkersneurofilament protein LNeurofilament ProteinsBiomarkerMultiple sclerosisNEDA-3Predictive valueSerum neurofilament light chain

Identifiers

PMID41803257
PMCPMC12971747

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