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

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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884145/
https://www.ncbi.nlm.nih.gov/pubmed/35237145
http://dx.doi.org/10.3389/fnagi.2022.783996
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author 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
author_facet 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
author_sort Margraf, Nils G.
collection PubMed
description 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(181)) 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(181) (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(181) (AUC 0.71). P-tau(181) (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.
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spelling pubmed-88841452022-03-01 Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis 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 Front Aging Neurosci Neuroscience 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(181)) 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(181) (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(181) (AUC 0.71). P-tau(181) (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. Frontiers Media S.A. 2022-02-14 /pmc/articles/PMC8884145/ /pubmed/35237145 http://dx.doi.org/10.3389/fnagi.2022.783996 Text en Copyright © 2022 Margraf, Jensen-Kondering, Weiler, Leypoldt, Maetzler, Philippen, Bartsch, Flüh, Röcken, Möller, Royl, Neumann, Brüggemann, Roeben, Schulte, Bender, Berg and Kuhlenbäumer. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
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
Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis
title Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis
title_full Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis
title_fullStr Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis
title_full_unstemmed Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis
title_short Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis
title_sort cerebrospinal fluid biomarkers in cerebral amyloid angiopathy: new data and quantitative meta-analysis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884145/
https://www.ncbi.nlm.nih.gov/pubmed/35237145
http://dx.doi.org/10.3389/fnagi.2022.783996
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