Amyloid- β and tau deposition influences cognitive and functional decline in Down syndrome

  • Monika Grigorova
  • , Elijah Mak
  • , Stephanie S.G. Brown
  • , Jessica Beresford-Webb
  • , Young T. Hong
  • , Tim D. Fryer
  • , Jonathan P. Coles
  • , Franklin I. Aigbirhio
  • , Dana Tudorascu
  • , Annie Cohen
  • , Bradley T. Christian
  • , Beau Ances
  • , Benjamin L. Handen
  • , Charles M. Laymon
  • , William E. Klunk
  • , Isabel C.H. Clare
  • , Anthony J. Holland
  • , Shahid H. Zaman

Research output: Contribution to journalArticlepeer-review

Abstract

This study investigates whether tau has (i) an independent effect from amyloid-β on changes in cognitive and functional performance and (ii) a synergistic relationship with amyloid-β in the exacerbation of decline in aging Down syndrome (DS). 105 participants with DS underwent baseline PET [18F]-AV1451 and PET [11C]PiB scans to quantify tau deposition in Braak regions II-VI and the Striatum and amyloid-β status respectively. Linear Mixed Effects models were implemented to assess how tau and amyloid-β deposition are related to change over three time points. Tau was a significant independent predictor of cognitive and functional change. The three-way interaction between time, [11C]PiB status and tau was significant in the models of episodic memory and visuospatial cognition. Baseline tau is a significant predictor of cognitive and functional decline, over and above the effect of amyloid-β status. Results suggest a synergistic relationship between amyloid-β status and tau as predictors of change in memory and visuospatial cognition.

Original languageEnglish
Pages (from-to)36-45
Number of pages10
JournalNeurobiology of Aging
Volume119
DOIs
StatePublished - Nov 2022

Keywords

  • Alzheimer's disease
  • Amyloid-β
  • Down syndrome
  • PET [C]PiB
  • PET [F]-AV1451
  • Tau

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