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Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals: Examining the Necessity to Adjust for Biomarker Status in Normative Data

We investigated whether amyloid-β (Aβ) and tau affected cognition in cognitively normal (CN) individuals, and whether norms for neuropsychological tests based on biomarker-negative individuals would improve early detection of dementia. We included 907 CN individuals from 8 European cohorts and from...

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Autores principales: Bos, Isabelle, Vos, Stephanie J. B., Jansen, Willemijn J., Vandenberghe, Rik, Gabel, Silvy, Estanga, Ainara, Ecay-Torres, Mirian, Tomassen, Jori, den Braber, Anouk, Lleó, Alberto, Sala, Isabel, Wallin, Anders, Kettunen, Petronella, Molinuevo, José L., Rami, Lorena, Chetelat, Gaël, de la Sayette, Vincent, Tsolaki, Magda, Freund-Levi, Yvonne, Johannsen, Peter, Novak, Gerald P., Ramakers, Inez, Verhey, Frans R., Visser, Pieter Jelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027060/
https://www.ncbi.nlm.nih.gov/pubmed/29988624
http://dx.doi.org/10.3389/fnagi.2018.00193
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author Bos, Isabelle
Vos, Stephanie J. B.
Jansen, Willemijn J.
Vandenberghe, Rik
Gabel, Silvy
Estanga, Ainara
Ecay-Torres, Mirian
Tomassen, Jori
den Braber, Anouk
Lleó, Alberto
Sala, Isabel
Wallin, Anders
Kettunen, Petronella
Molinuevo, José L.
Rami, Lorena
Chetelat, Gaël
de la Sayette, Vincent
Tsolaki, Magda
Freund-Levi, Yvonne
Johannsen, Peter
Novak, Gerald P.
Ramakers, Inez
Verhey, Frans R.
Visser, Pieter Jelle
author_facet Bos, Isabelle
Vos, Stephanie J. B.
Jansen, Willemijn J.
Vandenberghe, Rik
Gabel, Silvy
Estanga, Ainara
Ecay-Torres, Mirian
Tomassen, Jori
den Braber, Anouk
Lleó, Alberto
Sala, Isabel
Wallin, Anders
Kettunen, Petronella
Molinuevo, José L.
Rami, Lorena
Chetelat, Gaël
de la Sayette, Vincent
Tsolaki, Magda
Freund-Levi, Yvonne
Johannsen, Peter
Novak, Gerald P.
Ramakers, Inez
Verhey, Frans R.
Visser, Pieter Jelle
author_sort Bos, Isabelle
collection PubMed
description We investigated whether amyloid-β (Aβ) and tau affected cognition in cognitively normal (CN) individuals, and whether norms for neuropsychological tests based on biomarker-negative individuals would improve early detection of dementia. We included 907 CN individuals from 8 European cohorts and from the Alzheimer's disease Neuroimaging Initiative. All individuals were aged above 40, had Aβ status and neuropsychological data available. Linear mixed models were used to assess the associations of Aβ and tau with five neuropsychological tests assessing memory (immediate and delayed recall of Auditory Verbal Learning Test, AVLT), verbal fluency (Verbal Fluency Test, VFT), attention and executive functioning (Trail Making Test, TMT, part A and B). All test except the VFT were associated with Aβ status and this influence was augmented by age. We found no influence of tau on any of the cognitive tests. For the AVLT Immediate and Delayed recall and the TMT part A and B, we calculated norms in individuals without Aβ pathology (Aβ- norms), which we validated in an independent memory-clinic cohort by comparing their predictive accuracy to published norms. For memory tests, the Aβ- norms rightfully identified an additional group of individuals at risk of dementia. For non-memory test we found no difference. We confirmed the relationship between Aβ and cognition in cognitively normal individuals. The Aβ- norms for memory tests in combination with published norms improve prognostic accuracy of dementia.
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spelling pubmed-60270602018-07-09 Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals: Examining the Necessity to Adjust for Biomarker Status in Normative Data Bos, Isabelle Vos, Stephanie J. B. Jansen, Willemijn J. Vandenberghe, Rik Gabel, Silvy Estanga, Ainara Ecay-Torres, Mirian Tomassen, Jori den Braber, Anouk Lleó, Alberto Sala, Isabel Wallin, Anders Kettunen, Petronella Molinuevo, José L. Rami, Lorena Chetelat, Gaël de la Sayette, Vincent Tsolaki, Magda Freund-Levi, Yvonne Johannsen, Peter Novak, Gerald P. Ramakers, Inez Verhey, Frans R. Visser, Pieter Jelle Front Aging Neurosci Neurology We investigated whether amyloid-β (Aβ) and tau affected cognition in cognitively normal (CN) individuals, and whether norms for neuropsychological tests based on biomarker-negative individuals would improve early detection of dementia. We included 907 CN individuals from 8 European cohorts and from the Alzheimer's disease Neuroimaging Initiative. All individuals were aged above 40, had Aβ status and neuropsychological data available. Linear mixed models were used to assess the associations of Aβ and tau with five neuropsychological tests assessing memory (immediate and delayed recall of Auditory Verbal Learning Test, AVLT), verbal fluency (Verbal Fluency Test, VFT), attention and executive functioning (Trail Making Test, TMT, part A and B). All test except the VFT were associated with Aβ status and this influence was augmented by age. We found no influence of tau on any of the cognitive tests. For the AVLT Immediate and Delayed recall and the TMT part A and B, we calculated norms in individuals without Aβ pathology (Aβ- norms), which we validated in an independent memory-clinic cohort by comparing their predictive accuracy to published norms. For memory tests, the Aβ- norms rightfully identified an additional group of individuals at risk of dementia. For non-memory test we found no difference. We confirmed the relationship between Aβ and cognition in cognitively normal individuals. The Aβ- norms for memory tests in combination with published norms improve prognostic accuracy of dementia. Frontiers Media S.A. 2018-06-25 /pmc/articles/PMC6027060/ /pubmed/29988624 http://dx.doi.org/10.3389/fnagi.2018.00193 Text en Copyright © 2018 Bos, Vos, Jansen, Vandenberghe, Gabel, Estanga, Ecay-Torres, Tomassen, den Braber, Lleó, Sala, Wallin, Kettunen, Molinuevo, Rami, Chetelat, de la Sayette, Tsolaki, Freund-Levi, Johannsen, the Alzheimer's Disease Neuroimaging Initiative, Novak, Ramakers, Verhey and Visser. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Bos, Isabelle
Vos, Stephanie J. B.
Jansen, Willemijn J.
Vandenberghe, Rik
Gabel, Silvy
Estanga, Ainara
Ecay-Torres, Mirian
Tomassen, Jori
den Braber, Anouk
Lleó, Alberto
Sala, Isabel
Wallin, Anders
Kettunen, Petronella
Molinuevo, José L.
Rami, Lorena
Chetelat, Gaël
de la Sayette, Vincent
Tsolaki, Magda
Freund-Levi, Yvonne
Johannsen, Peter
Novak, Gerald P.
Ramakers, Inez
Verhey, Frans R.
Visser, Pieter Jelle
Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals: Examining the Necessity to Adjust for Biomarker Status in Normative Data
title Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals: Examining the Necessity to Adjust for Biomarker Status in Normative Data
title_full Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals: Examining the Necessity to Adjust for Biomarker Status in Normative Data
title_fullStr Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals: Examining the Necessity to Adjust for Biomarker Status in Normative Data
title_full_unstemmed Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals: Examining the Necessity to Adjust for Biomarker Status in Normative Data
title_short Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals: Examining the Necessity to Adjust for Biomarker Status in Normative Data
title_sort amyloid-β, tau, and cognition in cognitively normal older individuals: examining the necessity to adjust for biomarker status in normative data
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027060/
https://www.ncbi.nlm.nih.gov/pubmed/29988624
http://dx.doi.org/10.3389/fnagi.2018.00193
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