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Frontotemporal dementia is the leading cause of “true” A−/T+ profiles defined with Aβ(42/40) ratio

INTRODUCTION: Patients with positive tauopathy but negative Aβ(42) (A−T+) in the cerebrospinal fluid (CSF) represent a diagnostic challenge. The Aβ(42/40) ratio supersedes Aβ(42) and reintegrates “false” A−T+ patients into the Alzheimer's disease spectrum. However, the biomarker and clinical ch...

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Autores principales: Pouclet-Courtemanche, Hélène, Nguyen, Tri-Bao, Skrobala, Emilie, Boutoleau-Bretonnière, Claire, Pasquier, Florence, Bouaziz-Amar, Elodie, Bigot-Corbel, Edith, Schraen, Susanna, Dumurgier, Julien, Paquet, Claire, Lebouvier, Thibaud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378630/
https://www.ncbi.nlm.nih.gov/pubmed/30815533
http://dx.doi.org/10.1016/j.dadm.2019.01.001
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author Pouclet-Courtemanche, Hélène
Nguyen, Tri-Bao
Skrobala, Emilie
Boutoleau-Bretonnière, Claire
Pasquier, Florence
Bouaziz-Amar, Elodie
Bigot-Corbel, Edith
Schraen, Susanna
Dumurgier, Julien
Paquet, Claire
Lebouvier, Thibaud
author_facet Pouclet-Courtemanche, Hélène
Nguyen, Tri-Bao
Skrobala, Emilie
Boutoleau-Bretonnière, Claire
Pasquier, Florence
Bouaziz-Amar, Elodie
Bigot-Corbel, Edith
Schraen, Susanna
Dumurgier, Julien
Paquet, Claire
Lebouvier, Thibaud
author_sort Pouclet-Courtemanche, Hélène
collection PubMed
description INTRODUCTION: Patients with positive tauopathy but negative Aβ(42) (A−T+) in the cerebrospinal fluid (CSF) represent a diagnostic challenge. The Aβ(42/40) ratio supersedes Aβ(42) and reintegrates “false” A−T+ patients into the Alzheimer's disease spectrum. However, the biomarker and clinical characteristics of “true” and “false” A−T+ patients remain elusive. METHODS: Among the 509 T+N+ patients extracted from the databases of three memory clinics, we analyzed T+N+ patients with normal Aβ(42) and compared “false” A−T+ with abnormal Aβ(42/40) ratio and “true” A−T+ patients with normal Aβ(42/40) ratio, before CSF analysis and at follow-up. RESULTS: 24.9% of T+N+ patients had normal Aβ(42) levels. Among them, 42.7% were “true” A−T+. “True” A−T+ had lower CSF tau(P181) than “false” A−T+ patients. 48.0% of “true” A−T+ patients were diagnosed with frontotemporal lobar degeneration before CSF analysis and 64.0% at follow-up, as compared with 6% in the “false” A−T+ group (P < .0001). DISCUSSION: Frontotemporal lobar degeneration is probably the main cause of “true” A−T+ profiles.
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spelling pubmed-63786302019-02-27 Frontotemporal dementia is the leading cause of “true” A−/T+ profiles defined with Aβ(42/40) ratio Pouclet-Courtemanche, Hélène Nguyen, Tri-Bao Skrobala, Emilie Boutoleau-Bretonnière, Claire Pasquier, Florence Bouaziz-Amar, Elodie Bigot-Corbel, Edith Schraen, Susanna Dumurgier, Julien Paquet, Claire Lebouvier, Thibaud Alzheimers Dement (Amst) CSF Biomarkers INTRODUCTION: Patients with positive tauopathy but negative Aβ(42) (A−T+) in the cerebrospinal fluid (CSF) represent a diagnostic challenge. The Aβ(42/40) ratio supersedes Aβ(42) and reintegrates “false” A−T+ patients into the Alzheimer's disease spectrum. However, the biomarker and clinical characteristics of “true” and “false” A−T+ patients remain elusive. METHODS: Among the 509 T+N+ patients extracted from the databases of three memory clinics, we analyzed T+N+ patients with normal Aβ(42) and compared “false” A−T+ with abnormal Aβ(42/40) ratio and “true” A−T+ patients with normal Aβ(42/40) ratio, before CSF analysis and at follow-up. RESULTS: 24.9% of T+N+ patients had normal Aβ(42) levels. Among them, 42.7% were “true” A−T+. “True” A−T+ had lower CSF tau(P181) than “false” A−T+ patients. 48.0% of “true” A−T+ patients were diagnosed with frontotemporal lobar degeneration before CSF analysis and 64.0% at follow-up, as compared with 6% in the “false” A−T+ group (P < .0001). DISCUSSION: Frontotemporal lobar degeneration is probably the main cause of “true” A−T+ profiles. Elsevier 2019-02-15 /pmc/articles/PMC6378630/ /pubmed/30815533 http://dx.doi.org/10.1016/j.dadm.2019.01.001 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle CSF Biomarkers
Pouclet-Courtemanche, Hélène
Nguyen, Tri-Bao
Skrobala, Emilie
Boutoleau-Bretonnière, Claire
Pasquier, Florence
Bouaziz-Amar, Elodie
Bigot-Corbel, Edith
Schraen, Susanna
Dumurgier, Julien
Paquet, Claire
Lebouvier, Thibaud
Frontotemporal dementia is the leading cause of “true” A−/T+ profiles defined with Aβ(42/40) ratio
title Frontotemporal dementia is the leading cause of “true” A−/T+ profiles defined with Aβ(42/40) ratio
title_full Frontotemporal dementia is the leading cause of “true” A−/T+ profiles defined with Aβ(42/40) ratio
title_fullStr Frontotemporal dementia is the leading cause of “true” A−/T+ profiles defined with Aβ(42/40) ratio
title_full_unstemmed Frontotemporal dementia is the leading cause of “true” A−/T+ profiles defined with Aβ(42/40) ratio
title_short Frontotemporal dementia is the leading cause of “true” A−/T+ profiles defined with Aβ(42/40) ratio
title_sort frontotemporal dementia is the leading cause of “true” a−/t+ profiles defined with aβ(42/40) ratio
topic CSF Biomarkers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378630/
https://www.ncbi.nlm.nih.gov/pubmed/30815533
http://dx.doi.org/10.1016/j.dadm.2019.01.001
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