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Novel diagnostic and prognostic approach for rapidly progressive dementias: Indicators based on amyloid/tau/neurodegeneration (ATN) framework.

Authors :
Cheng, Yuan
Chen, Shu‐Fen
Zhang, Ya‐Ru
Guo, Yu
Wu, Kai‐Min
Huang, Yu‐Yuan
Aerqin, Qiaolifan
Kuo, Kevin
Li, Hong‐Qi
Chen, Shi‐Dong
Liu, Wei‐Shi
Dong, Qiang
Yu, Jin‐Tai
Source :
CNS Neuroscience & Therapeutics; Jul2024, Vol. 30 Issue 7, p1-12, 12p
Publication Year :
2024

Abstract

Aims: Apply established cerebrospinal fluid (CSF) and serum biomarkers and novel combined indicators based on the amyloid/tau/neurodegeneration (ATN) framework to improve diagnostic and prognostic power in patients with rapidly progressive dementias (RPDs). Methods: CSF and serum biomarkers of Alzheimer's disease (AD) common neuropathology including Aβ42, Aβ40, p‐Tau, and t‐Tau were measured in cognitively normal (CN) controls (n = 33) and three RPD groups with rapidly progressive AD (rpAD, n = 23), autoimmune encephalitis (AE, n = 25), and Creutzfeldt–Jakob disease (CJD, n = 28). Logistic regression and multiple linear regression were used for producing combined indicators and prognostic assessment, respectively, including A&T, A&N, T&N, A&T&N, etc. Results: Combined diagnostic indicator with A&T&N had the potential for differentiating AE from other types of RPDs, identifying 62.51% and 75% of AE subjects based on CSF and serum samples, respectively, compared to 39.13% and 37.5% when using autoantibodies. CSF t‐Tau was associated with survival in the CJD group (adjusted R‐Square = 0.16, p = 0.02), and its prognosis value improved when using combined predictors based on the ATN framework (adjusted R‐Square = 0.273, p = 0.014). Conclusion: Combined indicators based on the ATN framework provide a novel perspective for establishing biomarkers for early recognition of RPDs due to treatment‐responsive causes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17555930
Volume :
30
Issue :
7
Database :
Complementary Index
Journal :
CNS Neuroscience & Therapeutics
Publication Type :
Academic Journal
Accession number :
178814013
Full Text :
https://doi.org/10.1111/cns.14857