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Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring
Article . 2019 . Peer-reviewed
License: CC BY NC ND
Data sources: Crossref
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PubMed Central
Other literature type . 2019
License: CC BY NC ND
Data sources: PubMed Central
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UCL Discovery
Article . 2019
Data sources: UCL Discovery
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Plasma tau complements CSF tau and P‐tau in the diagnosis of Alzheimer's disease

Authors: Yi Li; Jaime Ramos Cejudo; Tracy Butler; Elizabeth Pirraglia; Jingyun Chen; Mony J. de Leon; Henrik Zetterberg; +5 Authors

Plasma tau complements CSF tau and P‐tau in the diagnosis of Alzheimer's disease

Abstract

AbstractIntroductionPlasma tau may be an accessible biomarker for Alzheimer's disease (AD), but the correlation between plasma and cerebrospinal fluid (CSF) tau and the value of combining plasma tau with CSF tau and phospho‐tau (P‐tau) are still unclear.MethodsPlasma‐tau, CSF‐tau, and P‐tau were measured in 97 subjects, including elderly cognitively normal controls (n = 68) and patients with AD (n = 29) recruited at the NYU Center for Brain Health, with comprehensive neuropsychological and magnetic resonance imaging evaluations.ResultsPlasma tau was higher in patients with AD than cognitively normal controls (P < .001, area under the receiver operating characteristic curve = 0.79) similarly to CSF tau and CSF P‐tau and was negatively correlated with cognition in AD. Plasma and CSF tau measures were poorly correlated. Adding plasma tau to CSF tau or CSF P‐tau significantly increased the areas under the receiver operating characteristic curve from 0.80 and 0.82 to 0.87 and 0.88, respectively.DiscussionPlasma tau is higher in AD independently from CSF‐tau. Importantly, adding plasma tau to CSF tau or P‐tau improves diagnostic accuracy, suggesting that plasma tau may represent a useful biomarker for AD, especially when added to CSF tau measures.

Country
United Kingdom
Keywords

Plasma tau, RC952-954.6, Special Section: Blood-Based Biomarkers for Alzheimer's Disease & Related Dementias. (Editor: Henrik Zetterberg), Blood biomarkers, CSF P-Tau, Cognition, Geriatrics, CSF tau, Neurology. Diseases of the nervous system, CSF P‐Tau, RC346-429, MRI

  • BIP!
    Impact byBIP!
    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    92
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 1%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
92
Top 1%
Top 10%
Top 1%
Green
Published in a Diamond OA journal