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A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer’s disease

Authors :
Barthélemy, Nicolas R.
Li, Yan
Joseph-Mathurin, Nelly
Gordon, Brian A.
Hassenstab, Jason
Benzinger, Tammie L.S.
Buckles, Virginia
Fagan, Anne M.
Perrin, Richard J.
Goate, Alison M.
Morris, John C.
Karch, Celeste M.
Xiong, Chengjie
Allegri, Ricardo
Mendez, Patricio Chrem
Berman, Sarah B.
Ikeuchi, Takeshi
Mori, Hiroshi
Shimada, Hiroyuki
Shoji, Mikio
Suzuki, Kazushi
Noble, James
Farlow, Martin
Chhatwal, Jasmeer
Graff-Radford, Neill R.
Salloway, Stephen
Schofield, Peter R.
Masters, Colin L.
Martins, Ralph N.
O'Connor, Antoinette
Fox, Nick C.
Levin, Johannes
Jucker, Mathias
Lehmann, Sylvain
Sato, Chihiro
Bateman, Randall J.
McDade, Eric
Dominantly Inherited Alzheimer Network
Barthélemy, Nicolas R.
Li, Yan
Joseph-Mathurin, Nelly
Gordon, Brian A.
Hassenstab, Jason
Benzinger, Tammie L.S.
Buckles, Virginia
Fagan, Anne M.
Perrin, Richard J.
Goate, Alison M.
Morris, John C.
Karch, Celeste M.
Xiong, Chengjie
Allegri, Ricardo
Mendez, Patricio Chrem
Berman, Sarah B.
Ikeuchi, Takeshi
Mori, Hiroshi
Shimada, Hiroyuki
Shoji, Mikio
Suzuki, Kazushi
Noble, James
Farlow, Martin
Chhatwal, Jasmeer
Graff-Radford, Neill R.
Salloway, Stephen
Schofield, Peter R.
Masters, Colin L.
Martins, Ralph N.
O'Connor, Antoinette
Fox, Nick C.
Levin, Johannes
Jucker, Mathias
Lehmann, Sylvain
Sato, Chihiro
Bateman, Randall J.
McDade, Eric
Dominantly Inherited Alzheimer Network
Source :
Research outputs 2014 to 2021
Publication Year :
2020

Abstract

Development of tau-based therapies for Alzheimer’s disease requires an understanding of the timing of disease-related changes in tau. We quantified the phosphorylation state at multiple sites of the tau protein in cerebrospinal fluid markers across four decades of disease progression in dominantly inherited Alzheimer’s disease. We identified a pattern of tau staging where site-specific phosphorylation changes occur at different periods of disease progression and follow distinct trajectories over time. These tau phosphorylation state changes are uniquely associated with structural, metabolic, neurodegenerative and clinical markers of disease, and some (p-tau217 and p-tau181) begin with the initial increases in aggregate amyloid-β as early as two decades before the development of aggregated tau pathology. Others (p-tau205 and t-tau) increase with atrophy and hypometabolism closer to symptom onset. These findings provide insights into the pathways linking tau, amyloid-β and neurodegeneration, and may facilitate clinical trials of tau-based treatments. © 2020, The Author(s), under exclusive licence to Springer Nature America, Inc.

Details

Database :
OAIster
Journal :
Research outputs 2014 to 2021
Publication Type :
Electronic Resource
Accession number :
edsoai.on1262100369
Document Type :
Electronic Resource