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Discriminative accuracy of the A/T/N scheme to identify cognitive impairment due to Alzheimer's disease
INTRODUCTION: The optimal combination of amyloid‐β/tau/neurodegeneration (A/T/N) biomarker profiles for the diagnosis of Alzheimer's disease (AD) dementia is unclear. METHODS: We examined the discriminative accuracy of A/T/N combinations assessed with neuroimaging biomarkers for the differentia...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886860/ https://www.ncbi.nlm.nih.gov/pubmed/36733847 http://dx.doi.org/10.1002/dad2.12390 |
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author | Pascoal, Tharick A. Leuzy, Antoine Therriault, Joseph Chamoun, Mira Lussier, Firoza Tissot, Cecile Strandberg, Olof Palmqvist, Sebastian Stomrud, Erik Ferreira, Pamela C. L. Ferrari‐Souza, João Pedro Smith, Ruben Benedet, Andrea Lessa Gauthier, Serge Hansson, Oskar Rosa‐Neto, Pedro |
author_facet | Pascoal, Tharick A. Leuzy, Antoine Therriault, Joseph Chamoun, Mira Lussier, Firoza Tissot, Cecile Strandberg, Olof Palmqvist, Sebastian Stomrud, Erik Ferreira, Pamela C. L. Ferrari‐Souza, João Pedro Smith, Ruben Benedet, Andrea Lessa Gauthier, Serge Hansson, Oskar Rosa‐Neto, Pedro |
author_sort | Pascoal, Tharick A. |
collection | PubMed |
description | INTRODUCTION: The optimal combination of amyloid‐β/tau/neurodegeneration (A/T/N) biomarker profiles for the diagnosis of Alzheimer's disease (AD) dementia is unclear. METHODS: We examined the discriminative accuracy of A/T/N combinations assessed with neuroimaging biomarkers for the differentiation of AD from cognitively unimpaired (CU) elderly and non‐AD neurodegenerative diseases in the TRIAD, BioFINDER‐1 and BioFINDER‐2 cohorts (total n = 832) using area under the receiver operating characteristic curves (AUC). RESULTS: For the diagnosis of AD dementia (vs. CU elderly), T biomarkers performed as well as the complete A/T/N system (AUC range: 0.90–0.99). A and T biomarkers in isolation performed as well as the complete A/T/N system in differentiating AD dementia from non‐AD neurodegenerative diseases (AUC range; A biomarker: 0.84–1; T biomarker: 0.83–1). DISCUSSION: In diagnostic settings, the use of A or T neuroimaging biomarkers alone can reduce patient burden and medical costs compared with using their combination, without significantly compromising accuracy. |
format | Online Article Text |
id | pubmed-9886860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98868602023-02-01 Discriminative accuracy of the A/T/N scheme to identify cognitive impairment due to Alzheimer's disease Pascoal, Tharick A. Leuzy, Antoine Therriault, Joseph Chamoun, Mira Lussier, Firoza Tissot, Cecile Strandberg, Olof Palmqvist, Sebastian Stomrud, Erik Ferreira, Pamela C. L. Ferrari‐Souza, João Pedro Smith, Ruben Benedet, Andrea Lessa Gauthier, Serge Hansson, Oskar Rosa‐Neto, Pedro Alzheimers Dement (Amst) Special Issue: Harmonization INTRODUCTION: The optimal combination of amyloid‐β/tau/neurodegeneration (A/T/N) biomarker profiles for the diagnosis of Alzheimer's disease (AD) dementia is unclear. METHODS: We examined the discriminative accuracy of A/T/N combinations assessed with neuroimaging biomarkers for the differentiation of AD from cognitively unimpaired (CU) elderly and non‐AD neurodegenerative diseases in the TRIAD, BioFINDER‐1 and BioFINDER‐2 cohorts (total n = 832) using area under the receiver operating characteristic curves (AUC). RESULTS: For the diagnosis of AD dementia (vs. CU elderly), T biomarkers performed as well as the complete A/T/N system (AUC range: 0.90–0.99). A and T biomarkers in isolation performed as well as the complete A/T/N system in differentiating AD dementia from non‐AD neurodegenerative diseases (AUC range; A biomarker: 0.84–1; T biomarker: 0.83–1). DISCUSSION: In diagnostic settings, the use of A or T neuroimaging biomarkers alone can reduce patient burden and medical costs compared with using their combination, without significantly compromising accuracy. John Wiley and Sons Inc. 2023-01-30 /pmc/articles/PMC9886860/ /pubmed/36733847 http://dx.doi.org/10.1002/dad2.12390 Text en © 2022 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Special Issue: Harmonization Pascoal, Tharick A. Leuzy, Antoine Therriault, Joseph Chamoun, Mira Lussier, Firoza Tissot, Cecile Strandberg, Olof Palmqvist, Sebastian Stomrud, Erik Ferreira, Pamela C. L. Ferrari‐Souza, João Pedro Smith, Ruben Benedet, Andrea Lessa Gauthier, Serge Hansson, Oskar Rosa‐Neto, Pedro Discriminative accuracy of the A/T/N scheme to identify cognitive impairment due to Alzheimer's disease |
title | Discriminative accuracy of the A/T/N scheme to identify cognitive impairment due to Alzheimer's disease |
title_full | Discriminative accuracy of the A/T/N scheme to identify cognitive impairment due to Alzheimer's disease |
title_fullStr | Discriminative accuracy of the A/T/N scheme to identify cognitive impairment due to Alzheimer's disease |
title_full_unstemmed | Discriminative accuracy of the A/T/N scheme to identify cognitive impairment due to Alzheimer's disease |
title_short | Discriminative accuracy of the A/T/N scheme to identify cognitive impairment due to Alzheimer's disease |
title_sort | discriminative accuracy of the a/t/n scheme to identify cognitive impairment due to alzheimer's disease |
topic | Special Issue: Harmonization |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886860/ https://www.ncbi.nlm.nih.gov/pubmed/36733847 http://dx.doi.org/10.1002/dad2.12390 |
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