Associations of cerebral amyloid beta and tau with cognition from midlife

Mitzi M. Gonzales, Adrienne O'Donnell, Saptaparni Ghosh, Emma Thibault, Jeremy Tanner, Claudia L. Satizabal, Charles S. Decarli, Georges El Fakhri, Keith A. Johnson, Alexa S. Beiser, Sudha Seshadri, Matthew Pase

Research output: Contribution to journalArticlepeer-review

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 Aβ 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 Aβ and tau. Higher fusiform tau associated with poorer visuospatial skills in younger adults. APOE ε4 interacted with Aβ and tau to worsen cognition across multiple domains.

Original languageEnglish (US)
Pages (from-to)5901-5911
Number of pages11
JournalAlzheimer's and Dementia
Volume20
Issue number9
DOIs
StatePublished - Sep 2024

Keywords

  • PET imaging
  • amyloid beta
  • cognition
  • midlife
  • tau

ASJC Scopus subject areas

  • Epidemiology
  • Health Policy
  • Developmental Neuroscience
  • Clinical Neurology
  • Geriatrics and Gerontology
  • Cellular and Molecular Neuroscience
  • Psychiatry and Mental health

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