Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25203
Title: Mesial temporal tau is related to worse cognitive performance and greater neocortical tau load in amyloid-β-negative cognitively normal individuals.
Austin Authors: Groot, Colin;Doré, Vincent ;Robertson, Joanne;Burnham, Samantha C;Savage, Greg;Ossenkoppele, Rik;Rowe, Christopher C ;Villemagne, Victor L 
Affiliation: Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
Centre of Excellence for Alzheimer's Disease Research and Care, School of Medical and Health Sciences, Edith Cowan University, Joondalup, Western Australia, Australia
Molecular Imaging and Therapy
Department of Psychology, Macquarie University, North Ryde, New South Wales, Australia
The Florey Institute, The University of Melbourne, Parkville, Victoria, Australia
CSIRO Health and Biosecurity, Parkville, Victoria, Australia
Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands; Clinical Memory Research Unit, Lund University, P663+Q9, Lund, Sweden..
Issue Date: 1-Oct-2020
metadata.dc.date: 2020-10-01
Publication information: Neurobiology of Aging 2020; 97: 41-48
Abstract: We examined whether mesial temporal (Me) tau relates to cognitive performance in 47 amyloid-β (Aβ)-negative, cognitively normal older adults (>60 years old). Me-tau was measured using [18F]flortaucipir-positron emission tomography standardized uptake value ratio. The effect of continuous and categorical (stratified at standardized uptake value ratio = 1.2 [21% Me-positive]) Me-tau on cognition (mini-mental state examination, pre-Alzheimer's cognitive composite, a memory composite, and a nonmemory composite score) was examined using general linear models, and associations between Me-tau and [18F]flortaucipir signal in the neocortex were assessed using voxelwise regressions (continuous) and voxelwise contrasts (categorical). In addition, we assessed the effect of age and Aβ burden on Me-tau. Both continuous and categorical Me-tau was associated with worse cognitive performance across all tests and with higher lateral temporal and parietal [18F]flortaucipir signal. Furthermore, we observed a marginal association between Me-tau and age, whereas there was no association with Aβ burden. Our findings indicate that Me-tau in Aβ-negative cognitively normal individuals, which is likely age-related (i.e., primary age-related tauopathy), might not be as benign as commonly thought.
URI: https://ahro.austin.org.au/austinjspui/handle/1/25203
DOI: 10.1016/j.neurobiolaging.2020.09.017
PubMed URL: 33130455
Type: Journal Article
Subjects: Mesial temporal lobe
PART
PET
Tau
Appears in Collections:Journal articles

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