Cortical thickness modeling and variability in Alzheimer's disease and frontotemporal dementia

dc.contributor.author
Pérez Millan, Agnès
dc.contributor.author
Borrego Écija, Sergi
dc.contributor.author
Falgàs Martínez, Neus
dc.contributor.author
Juncà Parella, Jordi
dc.contributor.author
Bosch Capdevila, Beatriz
dc.contributor.author
Tort Merino, Adrià
dc.contributor.author
Antonell Boixader, Anna, 1978-
dc.contributor.author
Bargalló Alabart, Núria
dc.contributor.author
Rami González, Lorena
dc.contributor.author
Balasa, Mircea
dc.contributor.author
Lladó Plarrumaní, Albert
dc.contributor.author
Sala Llonch, Roser
dc.contributor.author
Sánchez Valle, Raquel
dc.date.issued
2024-02-13T11:53:07Z
dc.date.issued
2024-02-13T11:53:07Z
dc.date.issued
2023-11-27
dc.date.issued
2024-02-08T16:14:14Z
dc.identifier
1432-1459
dc.identifier
https://hdl.handle.net/2445/207530
dc.identifier
745410
dc.identifier
9379384
dc.identifier
38012398
dc.identifier
850772
dc.description.abstract
Alzheimer's disease (AD) and frontotemporal dementia (FTD) show different patterns of cortical thickness (CTh) loss compared with healthy controls (HC), even though there is relevant heterogeneity between individuals suffering from each of these diseases. Thus, we developed CTh models to study individual variability in AD, FTD, and HC.We used the baseline CTh measures of 379 participants obtained from the structural MRI processed with FreeSurfer. A total of 169 AD patients (63 ± 9 years, 65 men), 88 FTD patients (64 ± 9 years, 43 men), and 122 HC (62 ± 10 years, 47 men) were studied. We fitted region-wise temporal models of CTh using Support Vector Regression. Then, we studied associations of individual deviations from the model with cerebrospinal fluid levels of neurofilament light chain (NfL) and 14-3-3 protein and Mini-Mental State Examination (MMSE). Furthermore, we used real longitudinal data from 144 participants to test model predictivity.We defined CTh spatiotemporal models for each group with a reliable fit. Individual deviation correlated with MMSE for AD and with NfL for FTD. AD patients with higher deviations from the trend presented higher MMSE values. In FTD, lower NfL levels were associated with higher deviations from the CTh prediction. For AD and HC, we could predict longitudinal visits with the presented model trained with baseline data. For FTD, the longitudinal visits had more variability.We highlight the value of CTh models for studying AD and FTD longitudinal changes and variability and their relationships with cognitive features and biomarkers.© 2023. The Author(s).
dc.format
11 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Springer Science and Business Media
dc.relation
Reproducció del document publicat a: https://doi.org/10.1007/s00415-023-12087-1
dc.relation
Journal of Neurology, 2023, vol. 271, p. 1428–1438
dc.relation
https://doi.org/10.1007/s00415-023-12087-1
dc.rights
cc-by (c) Pérez Millan et al., 2023
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Biomedicina)
dc.subject
Demència
dc.subject
Imatges per ressonància magnètica
dc.subject
Dementia
dc.subject
Magnetic resonance imaging
dc.title
Cortical thickness modeling and variability in Alzheimer's disease and frontotemporal dementia
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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