Evidence map›Paper›PMID 27042681›Full record

ArticleAnnals of clinical and translational neurology2016

Plasma neurofilament light chain predicts progression in progressive supranuclear palsy.

Julio C Rojas, Anna Karydas, Jee Bang, Richard M Tsai, Kaj Blennow, Victor Liman, Joel H Kramer, Howard Rosen, Bruce L Miller, Henrik Zetterberg and 1 more

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed, 4 pooled it
–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

121 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
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  16. Article
  17. Brain Atrophy Does Not Predict Clinical Progression in Progressive Supranuclear Palsy.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  18. Article
  19. Article
  20. Novel blood-based proteomic signatures across multiple neurodegenerative diseases.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article

61 more citing papers are in PubMed but not listed here.

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

11 authors.

Julio C RojasMemory and Aging Center Department of Neurology University of California, San Francisco San Francisco California.
Anna KarydasMemory and Aging Center Department of Neurology University of California, San Francisco San Francisco California.
Jee BangMemory and Aging Center Department of Neurology University of California, San Francisco San Francisco California.
Richard M TsaiMemory and Aging Center Department of Neurology University of California, San Francisco San Francisco California.
Kaj BlennowClinical Neurochemistry Laboratory Institute of Neuroscience and Physiology Sahlgrenska Academy at University of Gothenburg Sahlgrenska University Hospital Mölndal Sweden.
Victor LimanClinical Neurochemistry Laboratory Institute of Neuroscience and Physiology Sahlgrenska Academy at University of Gothenburg Sahlgrenska University Hospital Mölndal Sweden.
Joel H KramerMemory and Aging Center Department of Neurology University of California, San Francisco San Francisco California.
Howard RosenMemory and Aging Center Department of Neurology University of California, San Francisco San Francisco California.
Bruce L MillerMemory and Aging Center Department of Neurology University of California, San Francisco San Francisco California.
Henrik ZetterbergClinical Neurochemistry Laboratory Institute of Neuroscience and Physiology Sahlgrenska Academy at University of Gothenburg Sahlgrenska University Hospital Mölndal Sweden; Department of Molecular Neuroscience UCL Institute of Neurology Queen Square London United Kingdom.
Adam L BoxerMemory and Aging Center Department of Neurology University of California, San Francisco San Francisco California.

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
The Four Repeat Tauopathy Neuroimaging InitiativeR01AG038791 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOXER, ADAM L. · 2010 to 2020
$18.1M
Multidisciplinary Research Fellowship in Alzheimer’s disease and Related DementiasT32AG023481 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BRUCE L MILLER, HOWARD J ROSEN · 2005 to 2026
$7.4M
Training - The Frontotemporal Lobar Degeneration Clinical Research ConsortiumU54NS092089 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOXER, ADAM L. · 2014 to 2018
$6.4M
NIA NIH HHS P01 AG019724NIA NIH HHS R01 AG038791NIA NIH HHS T32 AG023481NINDS NIH HHS U54 NS092089
6 · The paper itself

Abstract

objectiveBlood-based biomarkers for neurodegenerative conditions could improve diagnosis and treatment development. Neurofilament light chain (NfL), a marker of axonal injury, is elevated in cerebrospinal fluid (CSF) of patients with progressive supranuclear palsy (PSP). The goal of this study was to determine the diagnostic and prognostic value of plasma NfL in patients with PSP.

methodsPlasma NfL was measured with ultrasensitive digital immunoassay-based technology at baseline and 1-year follow-up in a pilot cohort of 15 PSP patients and 12 healthy controls, and a validation cohort of 147 PSP patients. Mixed linear models tested the ability of plasma NfL to predict neurological, cognitive and functional decline, and brain atrophy.

resultsBaseline mean plasma NfL levels were elevated in PSP patients (31 ± 4 pg/mL, vs. control, 17.5 ± 1 pg/mL, P < 0.05) and this difference persisted at follow-up. A cutoff value of 20 pg/mL related to the diagnosis of PSP with a sensitivity of 0.80 and specificity of 0.83 (positive likelihood ratio = 4.7 and a negative likelihood radio of 0.24). Patients with higher NfL levels had more severe neurological (PSPRS, -36.9% vs. -28.9%, P = 0.04), functional (SEADL, -38.2% vs. -20%, P = 0.03), and neuropsychological (RBANS, -23.9% vs. -12.3%, P = 001) deterioration over 1 year. Higher baseline NfL predicted greater whole-brain and superior cerebellar peduncle volume loss. Plasma and CSF NfL were significantly correlated (r = 0.74, P = 0.002).

interpretationPlasma NfL is elevated in PSP and could be of value as a biomarker both to assist clinical diagnosis and to monitor pharmacodynamic effects on the neurodegenerative process in clinical trials.

Identifiers

PMID27042681
PMCPMC4774256

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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.