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Cross-sectional associations between [18F]GTP1 tau PET and cognition in Alzheimer's disease.
Teng, Edmond; Ward, Michael; Manser, Paul T; Sanabria-Bohorquez, Sandra; Ray, Rebecca D; Wildsmith, Kristin R; Baker, Suzanne; Kerchner, Geoffrey A; Weimer, Robby M.
Afiliación
  • Teng E; Early Clinical Development, Genentech, Inc., South San Francisco, CA, USA. Electronic address: teng.edmond@gene.com.
  • Ward M; Early Clinical Development, Genentech, Inc., South San Francisco, CA, USA.
  • Manser PT; Biostatistics, Genentech, Inc., South San Francisco, CA, USA.
  • Sanabria-Bohorquez S; Clinical Imaging Group, Genentech, Inc., South San Francisco, CA, USA.
  • Ray RD; Clinical Imaging Group, Genentech, Inc., South San Francisco, CA, USA; Early Clinical Development Informatics, Genentech, Inc., South San Francisco, CA, USA.
  • Wildsmith KR; Biomarker Development, Genentech, Inc., South San Francisco, CA, USA.
  • Baker S; Clinical Imaging Group, Genentech, Inc., South San Francisco, CA, USA; Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Kerchner GA; Early Clinical Development, Genentech, Inc., South San Francisco, CA, USA.
  • Weimer RM; Department of Biomedical Imaging, Genentech, Inc, South San Francisco, CA, USA.
Neurobiol Aging ; 81: 138-145, 2019 09.
Article en En | MEDLINE | ID: mdl-31280117
ABSTRACT
The regional relationships between tau positron emission tomography (PET) imaging and cognitive impairment in Alzheimer's disease (AD) remain uncertain. We examined cross-sectional associations between cognitive performance, cerebral uptake of the novel tau PET tracer [18F]GTP1, and other neuroimaging indices ([18F]florbetapir amyloid PET, magnetic resonance imaging) in 71 participants with normal cognition, prodromal AD, or AD dementia. Greater [18F]GTP1 uptake was seen with increasing clinical severity and correlated with poorer cognition. [18F]GTP1 uptake and cortical volume (but not [18F]florbetapir uptake) were independently associated with cognitive performance, particularly within the temporal lobe. Delayed memory was more specifically associated with temporal [18F]GTP1 uptake; other domains correlated with a broader range of regional [18F]GTP1 uptake. These data confirm that [18F]GTP1 tau PET uptake significantly correlates with cognitive performance in AD, but regional correlations between performance in non-memory cognitive domains were less specific than reported by tau PET imaging studies that included participants with atypical focal cortical AD syndromes. Tau PET imaging may have utility as a surrogate biomarker for clinical AD progression in therapeutic trials of disease-modifying interventions.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Encéfalo / Radioisótopos de Flúor / Proteínas tau / Cognición / Radiofármacos / Tomografía de Emisión de Positrones / Enfermedad de Alzheimer / Disfunción Cognitiva Tipo de estudio: Observational_studies / Prevalence_studies Idioma: En Revista: Neurobiol Aging Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Encéfalo / Radioisótopos de Flúor / Proteínas tau / Cognición / Radiofármacos / Tomografía de Emisión de Positrones / Enfermedad de Alzheimer / Disfunción Cognitiva Tipo de estudio: Observational_studies / Prevalence_studies Idioma: En Revista: Neurobiol Aging Año: 2019 Tipo del documento: Article