TY - JOUR
T1 - Amyloid-β, Tau, and Cognition in Cognitively Normal Older Individuals
T2 - Examining the Necessity to Adjust for Biomarker Status in Normative Data
AU - The Alzheimer's Disease Neuroimaging Initiative
AU - Bos, Isabelle
AU - Vos, Stephanie J.B.
AU - Jansen, Willemijn J.
AU - Vandenberghe, Rik
AU - Gabel, Silvy
AU - Estanga, Ainara
AU - Ecay-Torres, Mirian
AU - Tomassen, Jori
AU - den Braber, Anouk
AU - Lleó, Alberto
AU - Sala, Isabel
AU - Wallin, Anders
AU - Kettunen, Petronella
AU - Molinuevo, José L.
AU - Rami, Lorena
AU - Chetelat, Gaël
AU - de la Sayette, Vincent
AU - Tsolaki, Magda
AU - Freund-Levi, Yvonne
AU - Johannsen, Peter
AU - Novak, Gerald P.
AU - Ramakers, Inez
AU - Verhey, Frans R.
AU - Visser, Pieter Jelle
N1 - Funding Information:
Funding. The research leading to these results has received support from the Innovative Medicines Initiative Joint Undertaking under EMIF grant agreement n? 115372, resources of which are composed of financial contribution from the European Union's Seventh Framework Programme (FP7/2007-2013) and EFPIA companies' in kind contribution. The EDAR study was funded by the European Commission within the 5th framework program (contract # 37670). The Leuven cohort was funded by the Stichting voor Alzheimer Onderzoek (grant numbers #11020, #13007, and #15005). RV is a senior clinical investigator of the Flemish Research Foundation (FWO). The San Sebastian GAP study is partially funded by the Department of Health of the Basque Government (allocation 17.0.1.08.12.0000.2.454.01.41142.001.H). The Gothenburg MCI study was supported by Sahlgrenska University Hospital, Swedish Medical Research Council. The Alzheimer's Disease Neuroimaging Initiative (ADNI; National Institutes of Health Grant U01 AG024904 and DOD ADNI Department of Defense award number W81XWH-12-2-0012) was funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: Alzheimer's Association; Alzheimer's Drug Discovery Foundation; BioClinica, Inc.; Biogen Idec Inc.; Bristol-Myers Squibb Company; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; GE Healthcare; Innogenetics, N.V.; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Medpace, Inc.; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Synarc Inc.; and Takeda Pharmaceutical Company. The Canadian Institutes of Health Research is providing funds to Rev December 5, 2013 support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer's Disease Cooperative Study at the University of California, San Diego. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.
Publisher Copyright:
© 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.
PY - 2018/6/25
Y1 - 2018/6/25
N2 - 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.
AB - 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.
KW - Alzheimer's disease
KW - amyloid-beta
KW - cognition
KW - neuropsychological examination
KW - normative data
KW - tau
UR - https://www.scopus.com/pages/publications/85083388286
U2 - 10.3389/fnagi.2018.00193
DO - 10.3389/fnagi.2018.00193
M3 - Article
VL - 10
JO - Frontiers in aging neuroscience
JF - Frontiers in aging neuroscience
M1 - 193
ER -