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Spatial patterns of tau deposition are associated with amyloid, ApoE, sex, and cognitive decline in older adults.
Pereira, Joana B; Harrison, Theresa M; La Joie, Renaud; Baker, Suzanne L; Jagust, William J.
Afiliação
  • Pereira JB; Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institute, Stockholm, Sweden. joana.pereira@ki.se.
  • Harrison TM; Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden. joana.pereira@ki.se.
  • La Joie R; Helen Wills Neuroscience Institute, University of California Berkeley, Berkeley, CA, USA.
  • Baker SL; Memory and Aging Center, University of California, Oakland, CA, USA.
  • Jagust WJ; Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Eur J Nucl Med Mol Imaging ; 47(9): 2155-2164, 2020 08.
Article em En | MEDLINE | ID: mdl-31915896
ABSTRACT

PURPOSE:

The abnormal deposition of tau begins before the onset of clinical symptoms and seems to target specific brain networks. The aim of this study is to identify the spatial patterns of tau deposition in cognitively normal older adults and assess whether they are related to amyloid-ß (Aß), APOE, sex, and longitudinal cognitive decline.

METHODS:

We included 114 older adults with cross-sectional flortaucipir (FTP) and Pittsburgh Compound-B PET in addition to longitudinal cognitive testing. A voxel-wise independent component analysis was applied to FTP images to identify the spatial patterns of tau deposition. We then assessed whether tau within these patterns differed by Aß status, APOE genotype, and sex. Linear mixed effects models were built to test whether tau in each component predicted cognitive decline. Finally, we ordered the spatial components based on the frequency of high tau deposition to model tau spread.

RESULTS:

We found 10 biologically plausible tau patterns in the whole sample. There was greater tau in medial temporal, occipital, and orbitofrontal components in Aß-positive compared with Aß-negative individuals; in the parahippocampal component in ε3ε3 compared with ε2ε3 carriers; and in temporo-parietal and anterior frontal components in women compared with men. Higher tau in temporal and frontal components predicted longitudinal cognitive decline in memory and executive functions, respectively. Tau deposition was most frequently observed in medial temporal and ventral cortical areas, followed by lateral and primary areas.

CONCLUSIONS:

These findings suggest that the spatial patterns of tau in asymptomatic individuals are clinically meaningful and are associated with Aß, APOE ε2ε3, sex and cognitive decline. These patterns could be used to predict the regional spread of tau and perform in vivo tau staging in older adults.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Peptídeos beta-Amiloides / Proteínas tau / Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Peptídeos beta-Amiloides / Proteínas tau / Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article