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

dc.contributor.author
Tort Merino, Adrià
dc.contributor.author
Falgàs Martínez, Neus
dc.contributor.author
Allen, I. E.
dc.contributor.author
Balasa, M.
dc.contributor.author
Olives, Jaume
dc.contributor.author
Contador Muñana, José Miguel
dc.contributor.author
Castellví, M.
dc.contributor.author
Juncà Parella, J.
dc.contributor.author
Guillen, N.
dc.contributor.author
Borrego Écija, Sergi
dc.contributor.author
Bosch, B.
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Fernandez Villullas, G.
dc.contributor.author
Ramos Campoy, O.
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Antonell Boixader, Anna, 1978-
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Rami González, Lorena
dc.contributor.author
Sánchez Valle, Raquel
dc.contributor.author
Lladó Plarrumaní, Albert
dc.date.issued
2024-03-25T14:44:09Z
dc.date.issued
2024-03-25T14:44:09Z
dc.date.issued
2022-11-17
dc.date.issued
2023-07-06T08:22:42Z
dc.identifier
2328-9503
dc.identifier
https://hdl.handle.net/2445/209164
dc.identifier
9332623
dc.identifier
36398437
dc.description.abstract
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.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.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 ?4 status showed a significant effect on the decline of memory-related tasks within the EOAD cohort (p?<?0.05).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 ?4 status to a specific decline in memory performance in EOAD.© 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.
dc.format
12 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Wiley
dc.relation
Reproducció del document publicat a: https://doi.org/10.1002/acn3.51689
dc.relation
Annals Of Clinical And Translational Neurology, 2022, vol. 9, num. 12, p. 1962-1973
dc.relation
https://doi.org/10.1002/acn3.51689
dc.rights
cc by-nc-nd (c) Tort‐Merino, Adrià et al., 2022
dc.rights
http://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
dc.subject
Malaltia d'Alzheimer
dc.subject
Tests neuropsicològics
dc.subject
Alzheimer Disease
dc.subject
Neuropsychological Tests
dc.title
Early-onset Alzheimer's disease shows a distinct neuropsychological profile and more aggressive trajectories of cognitive decline than late-onset
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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