Evidence map›Paper›PMID 40654957›Full record

ArticlebioRxiv : the preprint server for biology2025

Measuring neurofilament light in human plasma and cerebrospinal fluid: a comparison of five analytical immunoassays.

Udit Sheth, Rebecca Harrison, Kyle Ferber, Erin G Rosenbaugh, Amanda Bevis, Rohini Khillan, Michael Benatar, Nicole L Bjorklund, Elena Di Daniel, Glenn A Harris and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Udit ShethDepartment of Neuroscience, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, United States.ORCID 0000-0003-4360-7892
Rebecca HarrisonAstex Pharmaceuticals, 436 Cambridge Science Park Milton Rd, Milton, Cambridge, CB4 0QA, United Kingdom.
Kyle FerberBiogen, Department of Biostatistics, 225 Binney Street, Cambridge, MA, 02142, United States.
Erin G RosenbaughFoundation at the National Institute of Health Inc., 11400 Rockville Pike, Suite 600, North Bethesda, MD, 20852, United States.
Amanda BevisFoundation at the National Institute of Health Inc., 11400 Rockville Pike, Suite 600, North Bethesda, MD, 20852, United States.
Rohini KhillanFoundation at the National Institute of Health Inc., 11400 Rockville Pike, Suite 600, North Bethesda, MD, 20852, United States.
Michael BenatarDepartment of Neurology and ALS Center, University of Miami Miller School of Medicine, Miami, FL, 33136, United States.
Nicole L BjorklundAssociation for Frontotemporal Degeneration, 2700 Horizon Drive, Suite 120, King of Prussia, PA, 19406, United States.
Elena Di DanielAstex Pharmaceuticals, 436 Cambridge Science Park Milton Rd, Milton, Cambridge, CB4 0QA, United Kingdom.
Glenn A HarrisRainwater Charitable Foundation, 777 Main Street, Suite 2250, Fort Worth, TX, 76102, United States.
Olga I KahnAlector, Inc., 131 Oyster Point Blvd, #600, South San Francisco, CA, 94080, United States.
Yongge LiuOtsuka Pharmaceutical Development & Commercialization, Inc, 2440 Research Blvd, Rockville, MD, 20850, United States.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Laura L MiticThe Bluefield Project to Cure Frontotemporal Dementia and the University of California, San Francisco, San Francisco, CA 94158, United States.
Danielle GrahamBiogen, Department of Biomarkers and Systems Biology, 225 Binney Street, Cambridge, MA, 02142, United States.
Tania F GendronDepartment of Neuroscience, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, United States.

Funding

Uncovering new genes and disease modifiers for ALS and related disordersU54NS092091 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Michael Benatar · 2014 to 2026
$19.8M
Multi-Center ALS Biomarker Validation Study (CReATe Biomarkers)U01NS107027 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BENATAR, MICHAEL, MALASPINA, ANDREA · 2018 to 2023
$3.5M
NINDS NIH HHS U01 NS107027NINDS NIH HHS U54 NS092091
6 · The paper itself

Abstract

Objectives: Neurofilament light (NfL) is an established biofluid marker of neuroaxonal injury for neurological diseases. Several high-throughput and sensitive immunoassays have been developed to quantify NfL in blood and cerebrospinal fluid (CSF), facilitating the use of NfL as a biomarker in research and clinical practice. However, because of the lack of rigorous comparisons of assays, it has been difficult to determine whether data are comparable and whether assay performance differs. Here, we compared the performance of five NfL immunoassays. Methods: To assess the five NfL immunoassays (Fujirebio, ProteinSimple, Quanterix, Roche and Siemens), we used pooled plasma or pooled CSF, as well as unique samples from 20 healthy controls and 20 individuals with El Escorial defined probable or definite amyotrophic lateral sclerosis (ALS), to evaluate precision, parallelism and/or bias. We also examined correlations between plasma and CSF NfL concentrations within and across assays and evaluated their ability to differentiate healthy controls from individuals with ALS. Results: Four of the five assays demonstrated exemplary performance based on our analyses of precision and parallelism. Across the five assays, NfL concentrations were lower in plasma than in CSF, although they displayed a high degree of correlation. We noted bias across assays; plasma NfL concentrations were lowest for the Roche assay and highest for the ProteinSimple assay. In addition, all assays reliably distinguished healthy controls from individuals with ALS using plasma or CSF NfL. Conclusions: Four NfL assays demonstrated similar analytic performance. Alongside performance, other factors such as costs, accessibility, useability, footprint, and intended use, should be considered.

Indexed as

amyotrophic lateral sclerosisbiomarkercerebrospinal fluidimmunoassaysneurofilament light chainplasma

Identifiers

PMID40654957
PMCPMC12247930

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.