<scp>ALS</scp> plasma biomarkers reveal neurofilament and <scp>pTau</scp> correlate with disease onset and progression

We confirm previous reports showing elevated pTau181 in ALS plasma and show elevation of other phosphorylated tau forms, pTau217 and pTau231, typically observed in Alzheimer's disease. We provide preliminary data showing the detection and elevation of pTDP-43-409/410 in a subset of ALS samples compared to healthy controls. Neurofilament and tau levels are highly correlated suggesting their elevation may reflect a common pathology and disease state. Total and phosphorylated tau are correlated with multiple disease measures, such as ALS duration, ALSFRS-R, and site of onset.

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Publication Details

Journal
Annals of Clinical and Translational Neurology
Published
2025-02-06
DOI
https://doi.org/10.1002/acn3.70001
Citations
13
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
18.06

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article

ALS plasma biomarkers reveal neurofilament and pTau correlate with disease onset and progression

C. Han, Zachary T. McEachin, Eleanor V. Thomas, Jonathan D. Glass et al.
13 citations
Annals of Clinical and Translational Neurology
Amyotrophic Lateral Sclerosis Research
18.06
article

ALS plasma biomarkers reveal neurofilament and pTau correlate with disease onset and progression

C. Han, Zachary T. McEachin, Eleanor V. Thomas, Jonathan D. Glass, Jennifer Taylor, Yingjie Li, Woo Jae Kim, Nicholas T. Seyfried, C. Fournier, Marla Gearing
article en
13 citations

Abstract

We confirm previous reports showing elevated pTau181 in ALS plasma and show elevation of other phosphorylated tau forms, pTau217 and pTau231, typically observed in Alzheimer's disease. We provide preliminary data showing the detection and elevation of pTDP-43-409/410 in a subset of ALS samples compared to healthy controls. Neurofilament and tau levels are highly correlated suggesting their elevation may reflect a common pathology and disease state. Total and phosphorylated tau are correlated with multiple disease measures, such as ALS duration, ALSFRS-R, and site of onset.

Annals of Clinical and Translational NeurologyVol. 12(4)
Emory University (US), University of Chicago (US)
American Academy of Neurology, National Institutes of Health, NIH Clinical Center
Good health and well-being
Openalex Percentile: Top 1%
Amyotrophic Lateral Sclerosis Research
18.06
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