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Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset

OBJECTIVES: Early‐ and late‐onset Alzheimer's disease (EOAD and LOAD) share the same neuropathological traits but show distinct cognitive features. We aimed to explore baseline and longitudinal outcomes of global and domain‐specific cognitive function in a well characterized cohort of patients...

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Autores principales: Tort‐Merino, Adrià, Falgàs, Neus, Allen, Isabel E., Balasa, Mircea, Olives, Jaume, Contador, José, Castellví, Magdalena, Juncà‐Parella, Jordi, Guillén, Núria, Borrego‐Écija, Sergi, Bosch, Bea, Fernández‐Villullas, Guadalupe, Ramos‐Campoy, Oscar, Antonell, Anna, Rami, Lorena, Sánchez‐Valle, Raquel, Lladó, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735361/
https://www.ncbi.nlm.nih.gov/pubmed/36398437
http://dx.doi.org/10.1002/acn3.51689
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author Tort‐Merino, Adrià
Falgàs, Neus
Allen, Isabel E.
Balasa, Mircea
Olives, Jaume
Contador, José
Castellví, Magdalena
Juncà‐Parella, Jordi
Guillén, Núria
Borrego‐Écija, Sergi
Bosch, Bea
Fernández‐Villullas, Guadalupe
Ramos‐Campoy, Oscar
Antonell, Anna
Rami, Lorena
Sánchez‐Valle, Raquel
Lladó, Albert
author_facet Tort‐Merino, Adrià
Falgàs, Neus
Allen, Isabel E.
Balasa, Mircea
Olives, Jaume
Contador, José
Castellví, Magdalena
Juncà‐Parella, Jordi
Guillén, Núria
Borrego‐Écija, Sergi
Bosch, Bea
Fernández‐Villullas, Guadalupe
Ramos‐Campoy, Oscar
Antonell, Anna
Rami, Lorena
Sánchez‐Valle, Raquel
Lladó, Albert
author_sort Tort‐Merino, Adrià
collection PubMed
description OBJECTIVES: Early‐ and late‐onset Alzheimer's disease (EOAD and LOAD) share the same neuropathological traits but show distinct cognitive features. We aimed to explore baseline and longitudinal outcomes of global and domain‐specific cognitive function in a well characterized cohort of patients with a biomarker‐based diagnosis. METHODS: In this retrospective cohort study, 195 participants were included and classified according to their age, clinical status, and CSF AD biomarker profile: 89 EOAD, 37 LOAD, 46 young healthy controls (age ≤ 65 years), and 23 old healthy controls (>65 years). All subjects underwent clinical and neuropsychological assessment, neuroimaging, APOE genotyping and lumbar puncture. RESULTS: We found distinct neuropsychological profiles between EOAD and LOAD at the time of diagnosis. Both groups showed similar performances on memory and language domains, but the EOAD patients displayed worsened deficits in visual perception, praxis, and executive tasks (p < 0.05). Longitudinally, cognitive decline in EOAD was more pronounced than LOAD in the global outcomes at the expense of these non‐amnestic domains. We found that years of education significantly influenced the decline in most of the neuropsychological tests. Besides, the APOE ε4 status showed a significant effect on the decline of memory‐related tasks within the EOAD cohort (p < 0.05). INTERPRETATION: Age of onset is a main factor shaping the cognitive trajectories in AD patients, with younger age driving to a steeper decline of the non‐memory domains. Years of education are related to a transversal decline in all cognitive domains and APOE ε4 status to a specific decline in memory performance in EOAD.
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spelling pubmed-97353612022-12-12 Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset Tort‐Merino, Adrià Falgàs, Neus Allen, Isabel E. Balasa, Mircea Olives, Jaume Contador, José Castellví, Magdalena Juncà‐Parella, Jordi Guillén, Núria Borrego‐Écija, Sergi Bosch, Bea Fernández‐Villullas, Guadalupe Ramos‐Campoy, Oscar Antonell, Anna Rami, Lorena Sánchez‐Valle, Raquel Lladó, Albert Ann Clin Transl Neurol Research Articles OBJECTIVES: Early‐ and late‐onset Alzheimer's disease (EOAD and LOAD) share the same neuropathological traits but show distinct cognitive features. We aimed to explore baseline and longitudinal outcomes of global and domain‐specific cognitive function in a well characterized cohort of patients with a biomarker‐based diagnosis. METHODS: In this retrospective cohort study, 195 participants were included and classified according to their age, clinical status, and CSF AD biomarker profile: 89 EOAD, 37 LOAD, 46 young healthy controls (age ≤ 65 years), and 23 old healthy controls (>65 years). All subjects underwent clinical and neuropsychological assessment, neuroimaging, APOE genotyping and lumbar puncture. RESULTS: We found distinct neuropsychological profiles between EOAD and LOAD at the time of diagnosis. Both groups showed similar performances on memory and language domains, but the EOAD patients displayed worsened deficits in visual perception, praxis, and executive tasks (p < 0.05). Longitudinally, cognitive decline in EOAD was more pronounced than LOAD in the global outcomes at the expense of these non‐amnestic domains. We found that years of education significantly influenced the decline in most of the neuropsychological tests. Besides, the APOE ε4 status showed a significant effect on the decline of memory‐related tasks within the EOAD cohort (p < 0.05). INTERPRETATION: Age of onset is a main factor shaping the cognitive trajectories in AD patients, with younger age driving to a steeper decline of the non‐memory domains. Years of education are related to a transversal decline in all cognitive domains and APOE ε4 status to a specific decline in memory performance in EOAD. John Wiley and Sons Inc. 2022-11-17 /pmc/articles/PMC9735361/ /pubmed/36398437 http://dx.doi.org/10.1002/acn3.51689 Text en © 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Tort‐Merino, Adrià
Falgàs, Neus
Allen, Isabel E.
Balasa, Mircea
Olives, Jaume
Contador, José
Castellví, Magdalena
Juncà‐Parella, Jordi
Guillén, Núria
Borrego‐Écija, Sergi
Bosch, Bea
Fernández‐Villullas, Guadalupe
Ramos‐Campoy, Oscar
Antonell, Anna
Rami, Lorena
Sánchez‐Valle, Raquel
Lladó, Albert
Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset
title Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset
title_full Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset
title_fullStr Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset
title_full_unstemmed Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset
title_short Early‐onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset
title_sort early‐onset alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late‐onset
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735361/
https://www.ncbi.nlm.nih.gov/pubmed/36398437
http://dx.doi.org/10.1002/acn3.51689
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