Evidence map›Paper›PMID 37577499›Full record

ArticleResearch square2023

Neurofilament Light Chain in Spinal Fluid and Plasma in Multiple System Atrophy - A Prospective, Longitudinal Biomarker Study.

Wolfgang Singer, Ann M Schmeichel, David M Sletten, Tonette L Gehrking, Jade A Gehrking, Jorge Trejo-Lopez, Mariana D Suarez, Jennifer K Anderson, Pamela H Bass, Timothy G Lesnick and 1 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. 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, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Wolfgang SingerDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0003-1263-6850
Ann M SchmeichelDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
David M SlettenDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Tonette L GehrkingDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Jade A GehrkingDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Jorge Trejo-LopezDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Mariana D SuarezDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Jennifer K AndersonDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Pamela H BassDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Timothy G LesnickDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Phillip A LowDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic · US

Funding

Project: Predicting PhenoconversionU19AG071754 · NIA · WASHINGTON UNIVERSITY · PI Ronald Postuma · 2021 to 2026
$41.2M
Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Synucleinopathies – Novel Targets in Early Diagnosis, Pathophysiology, and Therapeutic ApproachR01NS092625 · NINDS · MAYO CLINIC ROCHESTER · PI SINGER, WOLFGANG, VEMURI, PRASHANTHI · 2015 to 2025
$6.6M
Randomized Double-Blind Placebo-Controlled Adaptive Design Trial of Intrathecally Administered Autologous Mesenchymal Stem Cells in Multiple System AtrophyR01FD007290 · FDA · MAYO CLINIC ROCHESTER · PI SINGER, WOLFGANG · 2021 to 2024
$3.2M
FDA HHS R01 FD007290NCATS NIH HHS UL1 TR000135NIA NIH HHS U19 AG071754NINDS NIH HHS R01 NS092625
6 · The paper itself

Abstract

Purpose There is a critical need for reliable diagnostic biomarkers as well as surrogate markers of disease progression in multiple system atrophy (MSA). Neurofilament light chain (NfL) has been reported to potentially meet those needs. We therefore sought to explore the value of NfL in plasma (NfL-p) in contrast to CSF (NfL-c) as diagnostic marker of MSA, and to assess NfL-p and NfL-c as markers of clinical disease progression. Methods Well-characterized patients with early MSA (n=32), Parkinson's disease (PD, n=21), and matched controls (CON, n=15) were enrolled in a prospective, longitudinal study of synucleinopathies with serial annual evaluations. NfL was measured using a high sensitivity immunoassay, and findings were assessed by disease category and relationship with clinical measures of disease progression. Results Measurements of NfL-c were highly reproducible across immunoassay platforms (Pearson,r=0.99), while correlation between NfL-c and -p was only moderate (r=0.66). NfL was significantly higher in MSA compared to CON and PD; the separation was essentially perfect for NfL-c, but there was overlap, particularly with PD, for NfL-p. While clinical measures of disease severity progressively increased over time, NfL-c and -p remained at stable elevated levels within subjects across serial measurements. Neither change in NfL nor baseline NfL were significantly associated with changes in clinical markers of disease severity. Conclusions These findings confirm NfL-c as faithful diagnostic marker of MSA, while NfL-p showed less robust diagnostic value. The significant NfL elevation in MSA was found to be remarkably stable over time and was not predictive of clinical disease progression.

Identifiers

PMID37577499
PMCPMC10418538
OpenAlexW4385462805

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.