Evidence map›Paper›PMID 36427295›Full record

ArticleAnnals of clinical and translational neurology2023

Associations of sNfL with clinico-radiological measures in a large MS population.

Elias S Sotirchos, Kathryn C Fitzgerald, Carol M Singh, Matthew D Smith, Maria Reyes-Mantilla, Carrie M Hersh, Megan H Hyland, Ryan Canissario, Sarah B Simmons, Georgina Arrambide and 13 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07225361 (Ublituximab), which is not on this map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% of its field
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.

NCT07225361 phase4recruitingnot on this mapstarted 2025, after this paper: background citation

Ublituximab (Briumvi) for Early Forms of Relapsing Multiple Sclerosis

TypeinterventionalSponsorNorthwestern UniversityRan2025 to 2029Enrolled40ConditionsMultiple Sclerosis, Multiple Sclerosis (MS) - Relapsing-remittingArmsUblituximab
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Choosing initial MS therapy; personal, disease, and medication factors.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  7. Review
  8. Contribution of Blood Biomarkers to Multiple Sclerosis Diagnosis.Neurology(R) neuroimmunology & neuroinflammation · 2025
    Article
  9. Renal function's impact on serum neurofilament levels in patients with multiple sclerosis: an exploratory analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 9 institutions in 3 countries.

Elias S SotirchosDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-8812-1637
Kathryn C FitzgeraldDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0003-3137-0322
Carol M SinghBiogen, Cambridge, Massachusetts, USA.
Matthew D SmithDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Maria Reyes-MantillaDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Carrie M HershLou Ruvo Center for Brain Health, Cleveland Clinic, Las Vegas, Nevada, USA.
Megan H HylandDepartment of Neurology, University of Rochester Medical Center, Rochester, New York, USA.
Ryan CanissarioDepartment of Neurology, University of Rochester Medical Center, Rochester, New York, USA.
Sarah B SimmonsMellen Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Georgina ArrambideDepartment of Neurology and Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, Barcelona, Spain.
Xavier MontalbanDepartment of Neurology and Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, Barcelona, Spain.
Manuel ComabellaDepartment of Neurology and Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID 0000-0002-2373-6657
Robert T NaismithDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Min QiaoDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri, USA.
Lauren B KruppDepartment of Neurology, New York University, New York City, New York, USA.ORCID 0000-0001-7003-807X
Jacqueline A NicholasOhioHealth Multiple Sclerosis Center, Riverside Methodist Hospital, Columbus, Ohio, USA.
Katja AkgünCenter of Clinical Neuroscience, Department of Neurology, University Clinic Carl-Gustav Carus, Dresden, Germany.
Tjalf ZiemssenCenter of Clinical Neuroscience, Department of Neurology, University Clinic Carl-Gustav Carus, Dresden, Germany.ORCID 0000-0001-8799-8202
Richard Rudick(formerly) Biogen, Cambridge, Massachusetts, USA.
Elizabeth FisherBiogen, Cambridge, Massachusetts, USA.
Robert A BermelMellen Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Ellen M MowryDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Peter A CalabresiDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-7776-6472
Johns Hopkins University · USBiogen (United States) · USCleveland Clinic · USUniversitat Autònoma de Barcelona · ESUniversity Hospital Carl Gustav Carus · DEUniversity of Rochester Medical Center · USWashington University in St. Louis · USCity University of New York · USOhioHealth · US

Funding

Validation of Serum Neurofilament Light Chain as a Prognostic and Monitoring Biomarker in Multiple SclerosisU01NS111678 · NINDS · JOHNS HOPKINS UNIVERSITY · PI CALABRESI, PETER A · 2020 to 2024
$6.3M
Prediction of risk of disability worsening and inflammatory disease activity in MS utilizing multimodal prediction algorithmsK23NS117883 · NINDS · JOHNS HOPKINS UNIVERSITY · PI SOTIRCHOS, ELIAS S · 2020 to 2024
$918k
Circadian Rhythms and Sleep, Structural Neuroimaging and Depression in People with Multiple SclerosisK01MH121582 · NIMH · JOHNS HOPKINS UNIVERSITY · PI FITZGERALD, KATHRYN C. · 2019 to 2022
$675k
NIH HHS K01MH121582NIH HHS K23NS117883NIH HHS U01NS111678NIMH NIH HHS K01 MH121582NINDS NIH HHS K23 NS117883NINDS NIH HHS U01 NS111678
6 · The paper itself

Abstract

objectiveEvaluation of serum neurofilament light chain (sNfL), measured using high-throughput assays on widely accessible platforms in large, real-world MS populations, is a critical step for sNfL to be utilized in clinical practice.

methodsMultiple Sclerosis Partners Advancing Technology and Health Solutions (MS PATHS) is a network of healthcare institutions in the United States and Europe collecting standardized clinical/imaging data and biospecimens during routine clinic visits. sNfL was measured in 6974 MS and 201 healthy control (HC) participants, using a high-throughput, scalable immunoassay.

resultsElevated sNfL levels for age (sNfL-E) were found in 1238 MS participants (17.8%). Factors associated with sNfL-E included male sex, younger age, progressive disease subtype, diabetes mellitus, impaired renal function, and active smoking. Higher body mass index (BMI) was associated with lower odds of elevated sNfL. Active treatment with disease-modifying therapy was associated with lower odds of sNfL-E. MS participants with sNfL-E exhibited worse neurological function (patient-reported disability, walking speed, manual dexterity, and cognitive processing speed), lower brain parenchymal fraction, and higher T2 lesion volume. Longitudinal analyses revealed accelerated short-term rates of whole brain atrophy in sNfL-E participants and higher odds of new T2 lesion development, although both MS participants with or without sNfL-E exhibited faster rates of whole brain atrophy compared to HC. Findings were consistent in analyses examining age-normative sNfL Z-scores as a continuous variable.

interpretationElevated sNfL is associated with clinical disability, inflammatory disease activity, and whole brain atrophy in MS, but interpretation needs to account for comorbidities including impaired renal function, diabetes, and smoking.

Indexed as

BrainAtrophyBiomarkersEuropeHumansMaleBiomarkers

Identifiers

PMID36427295
PMCPMC9852396
OpenAlexW4310082979

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Registered trials

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.