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Tau and atrophy: domain-specific relationships with cognition

Authors :
Leonardino A. Digma
Emilie T. Reas
James B. Brewer
Alzheimer’s Disease Neuroimaging Initiative
Anders M. Dale
Sarah J. Banks
John Madsen
Source :
Alzheimer’s Research & Therapy, Vol 11, Iss 1, Pp 1-12 (2019), Alzheimer's Research & Therapy, Alzheimer's research & therapy, vol 11, iss 1
Publication Year :
2019
Publisher :
BMC, 2019.

Abstract

Background Late-onset Alzheimer’s disease (AD) is characterized by primary memory impairment, which then progresses towards severe deficits across cognitive domains. Here, we report how performance in cognitive domains relates to patterns of tau deposition and cortical thickness. Methods We analyzed data from 131 amyloid-β positive participants (55 cognitively normal, 46 mild cognitive impairment, 30 AD) of the Alzheimer’s Disease Neuroimaging Initiative who underwent magnetic resonance imaging (MRI), flortaucipir (FTP) positron emission tomography, and neuropsychological testing. Surface-based vertex-wise and region-of-interest analyses were conducted between FTP and cognitive test scores, and between cortical thickness and cognitive test scores. Results FTP and thickness were differentially related to cognitive performance in several domains. FTP-cognition associations were more widespread than thickness-cognition associations. Further, FTP-cognition patterns reflected cortical systems that underlie different aspects of cognition. Conclusions Our findings indicate that AD-related decline in domain-specific cognitive performance reflects underlying progression of tau and atrophy into associated brain circuits. They also suggest that tau-PET may have better sensitivity to this decline than MRI-derived measures of cortical thickness. Electronic supplementary material The online version of this article (10.1186/s13195-019-0518-8) contains supplementary material, which is available to authorized users.

Details

Language :
English
ISSN :
17589193
Volume :
11
Issue :
1
Database :
OpenAIRE
Journal :
Alzheimer’s Research & Therapy
Accession number :
edsair.doi.dedup.....4e94f02fbc9762076bd903c63207b7a7