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Associations of cerebral amyloid beta and tau with cognition from midlife.
Gonzales, Mitzi M; O'Donnell, Adrienne; Ghosh, Saptaparni; Thibault, Emma; Tanner, Jeremy; Satizabal, Claudia L; Decarli, Charles S; Fakhri, Georges El; Johnson, Keith A; Beiser, Alexa S; Seshadri, Sudha; Pase, Matthew.
Afiliación
  • Gonzales MM; Department of Neurology, Cedars Sinai Medical Center, Los Angeles, California, USA.
  • O'Donnell A; Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Ghosh S; Department of Neurology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Thibault E; The Framingham Heart Study, Framingham, Massachusetts, USA.
  • Tanner J; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Satizabal CL; The Framingham Heart Study, Framingham, Massachusetts, USA.
  • Decarli CS; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
  • Fakhri GE; Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
  • Johnson KA; Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Beiser AS; Department of Neurology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Seshadri S; Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Pase M; The Framingham Heart Study, Framingham, Massachusetts, USA.
Alzheimers Dement ; 2024 Jul 22.
Article en En | MEDLINE | ID: mdl-39039896
ABSTRACT

INTRODUCTION:

Understanding early neuropathological changes and their associations with cognition may aid dementia prevention. This study investigated associations of cerebral amyloid and tau positron emission tomography (PET) retention with cognition in a predominately middle-aged community-based cohort and examined factors that may modify these relationships.

METHODS:

11C-Pittsburgh compound B amyloid and 18F-flortaucipir tau PET imaging were performed. Associations of amyloid and tau PET with cognition were evaluated using linear regression. Interactions with age, apolipoprotein E (APOE) ε4 status, and education were examined.

RESULTS:

Amyloid and tau PET were not associated with cognition in the overall sample (N = 423; mean 57 ± 10 years; 50% female). However, younger age (< 55 years) and APOE ε4 were significant effect modifiers, worsening cognition in the presence of higher amyloid and tau.

DISCUSSION:

Higher levels of Aß and tau may have a pernicious effect on cognition among APOE ε4 carriers and younger adults, suggesting a potential role for targeted early interventions. HIGHLIGHTS Risk and resilience factors influenced cognitive vulnerability due to Aß and tau. Higher fusiform tau associated with poorer visuospatial skills in younger adults. APOE ε4 interacted with Aß and tau to worsen cognition across multiple domains.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Alzheimers Dement Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Alzheimers Dement Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos