Evidence map›Paper›PMID 35309573›Full record

ArticleFrontiers in neurology2022

Evaluation of Plasma Neurofilament Light Chain Levels as a Biomarker of Neuronal Injury in the Active and Chronic Phases of Autoimmune Neurologic Disorders.

Ryan Kammeyer, Christopher Mizenko, Stefan Sillau, Alanna Richie, Gregory Owens, Kavita V Nair, Enrique Alvarez, Timothy L Vollmer, Jeffrey L Bennett, Amanda L Piquet

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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.

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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Neuroglial markers of damage in autoimmune neurology.Therapeutic advances in neurological disorders · 2026
    Review
  3. Review
  4. Increase of Plasma Biomarkers in Friedreich's Ataxia: Potential Insights into Disease Pathology.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  5. Article
  6. Cognitive dysfunction in pediatric systemic lupus erythematosus: current knowledge and future directions.Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence · 2024
    Review
  7. Review
  8. Review
  9. Review
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 at 1 institution in 1 country.

Ryan KammeyerDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Christopher MizenkoDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Stefan SillauDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Alanna RichieDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Gregory OwensDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Kavita V NairDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Enrique AlvarezDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Timothy L VollmerDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Jeffrey L BennettDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Amanda L PiquetDepartment of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
University of Colorado Anschutz Medical Campus · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To evaluate plasma neurofilament light (NfL) levels in autoimmune neurologic disorders (AINDs) and autoimmune encephalitis (AE). Background: Each particular neural autoantibody syndrome has a different clinical phenotype, making one unifying clinical outcome measure difficult to assess. While this is a heterogeneous group of disorders, the final common pathway is likely CNS damage and inflammation. Defining a biomarker of CNS injury that is easily obtainable through a blood sample and reflects a positive treatment response would be highly advantageous in future therapeutic trials. Measurement of blood concentration of neurofilament light (NfL) chain, however, may provide a biomarker of central nervous system (CNS) injury in AE and other AINDs. Here we provide an initial evaluation of plasma NfL levels in AE as well as other AINDs during active and chronic phases of disease and demonstrate its potential utility as a minimally-invasive biomarker for AE and AINDs. Design/Methods: Patients were retrospectively identified who were enrolled in the biorepository at the Rocky Mountain MS Center at the University of Colorado, or were prospectively enrolled after initial presentation. Patients had a well-defined AIND and were followed between 2014 and 2021. NfL was tested using the Single Molecule Array (SIMOA) technology. Patients with headaches but without other significant neurologic disease were included as controls. Results: Twenty-six plasma and 14 CSF samples of patients with AINDs, and 20 plasma control samples stored in the biorepository were evaluated. A positive correlation was found between plasma and CSF NfL levels for patients with an AIND ( Conclusions: Our findings support the use of plasma NfL as a potential minimally-invasive biomarker of CNS injury.

Indexed as

autoimmune encephalitis (AE)autoimmune neurological disordersbiomarkercerebellar ataxianeurofilament light (NfL) chainneurofilament (NF)

Identifiers

PMID35309573
PMCPMC8924486
OpenAlexW4214841315

What OpenQuestion holds

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Registered trials

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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.