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Cerebrospinal Fluid Classical Biomarker Levels in Mixed vs. Pure A + T + (A + T 1 +) Alzheimer's Disease.

Authors :
Tsantzali, Ioanna
Athanasaki, Athanasia
Boufidou, Fotini
Constantinides, Vasilios C.
Stefanou, Maria-Ioanna
Moschovos, Christos
Zompola, Christina
Paraskevas, Sotirios G.
Bonakis, Anastasios
Giannopoulos, Sotirios
Tsivgoulis, Georgios
Kapaki, Elisabeth
Paraskevas, George P.
Source :
Biomedicines; Dec2024, Vol. 12 Issue 12, p2904, 14p
Publication Year :
2024

Abstract

Background: Alzheimer's disease (AD) may present with pure (typical or atypical) and mixed phenotypes, sometimes causing difficulties in (differential) diagnosis. In order to achieve a diagnostic accuracy as high as possible, the diagnosis of AD during life depends on various biomarkers, including the cerebrospinal fluid (CSF) biomarkers. Methods: Classical CSF AD biomarkers were determined in a total of 61 patients, classified as both beta amyloid- and tau-positive A<superscript>+</superscript>T<superscript>+</superscript> (or A<superscript>+</superscript>T<subscript>1</subscript><superscript>+</superscript> according to the recently revised Alzheimer Association criteria for diagnosis and staging of AD). Twenty one of these patients fulfilled the criteria for mixed AD (mixed with Lewy bodies, cerebrovascular disease, or normal pressure hydrocephalus), whilst 40 had pure AD. Results: Patients did not differ with respect to gender, education, disease duration, and cognitive status. After controlling for confounding factors, no difference was observed between mixed and pure AD groups in Aβ<subscript>42</subscript> or Aβ<subscript>42</subscript>/Aβ<subscript>40</subscript> levels. Although by definition, patients of both groups had abnormal (increased) levels of phospho-tau<subscript>181</subscript>, the mixed AD group presented with lower (less abnormal) levels of phospho-tau181 and total tau as compared to the pure group. Conclusions: In patients with AD of comparable cognitive status, mixed AD cases may present with lower levels of tau proteins and, if close to the cut-off values, diagnostic uncertainty may be increased. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22279059
Volume :
12
Issue :
12
Database :
Complementary Index
Journal :
Biomedicines
Publication Type :
Academic Journal
Accession number :
181955600
Full Text :
https://doi.org/10.3390/biomedicines12122904