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Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis.

Authors :
Margraf, Nils G.
Jensen-Kondering, Ulf
Weiler, Caroline
Leypoldt, Frank
Maetzler, Walter
Philippen, Sarah
Bartsch, Thorsten
Flüh, Charlotte
Röcken, Christoph
Möller, Bettina
Royl, Georg
Neumann, Alexander
Brüggemann, Norbert
Roeben, Benjamin
Schulte, Claudia
Bender, Benjamin
Berg, Daniela
Kuhlenbäumer, Gregor
Source :
Frontiers in Aging Neuroscience; 2/14/2022, Vol. 14, p1-11, 11p
Publication Year :
2022

Abstract

Background: To evaluate the diagnostic accuracy of cerebrospinal fluid (CSF) biomarkers in patients with probable cerebral amyloid angiopathy (CAA) according to the modified Boston criteria in a retrospective multicentric cohort. Methods: Beta-amyloid 1-40 (Aβ40), beta-amyloid 1-42 (Aβ42), total tau (t-tau), and phosphorylated tau 181 (p-tau<superscript>181</superscript>) were measured in 31 patients with probable CAA, 28 patients with Alzheimer's disease (AD), and 30 controls. Receiver-operating characteristics (ROC) analyses were performed for the measured parameters as well as the Aβ42/40 ratio to estimate diagnostic parameters. A meta-analysis of all amenable published studies was conducted. Results: In our data Aβ42/40 (AUC 0.88) discriminated best between CAA and controls while Aβ40 did not perform well (AUC 0.63). Differentiating between CAA and AD, p-tau<superscript>181</superscript> (AUC 0.75) discriminated best in this study while Aβ40 (AUC 0.58) and Aβ42 (AUC 0.54) provided no discrimination. In the meta-analysis, Aβ42/40 (AUC 0.90) showed the best discrimination between CAA and controls followed by t-tau (AUC 0.79), Aβ40 (AUC 0.76), and p-tau<superscript>181</superscript> (AUC 0.71). P-tau<superscript>181</superscript> (AUC 0.76), Aβ40 (AUC 0.73), and t-tau (AUC 0.71) differentiated comparably between AD and CAA while Aβ42 (AUC 0.54) did not. In agreement with studies examining AD biomarkers, Aβ42/40 discriminated excellently between AD and controls (AUC 0.92–0.96) in this study as well as the meta-analysis. Conclusion: The analyzed parameters differentiate between controls and CAA with clinically useful accuracy (AUC > ∼0.85) but not between CAA and AD. Since there is a neuropathological, clinical and diagnostic continuum between CAA and AD, other diagnostic markers, e.g., novel CSF biomarkers or other parameters might be more successful. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16634365
Volume :
14
Database :
Complementary Index
Journal :
Frontiers in Aging Neuroscience
Publication Type :
Academic Journal
Accession number :
155230495
Full Text :
https://doi.org/10.3389/fnagi.2022.783996