Amyloid beta associations with connected speech in cognitively unimpaired adults
- PMID: 34095435
- PMCID: PMC8158164
- DOI: 10.1002/dad2.12203
Amyloid beta associations with connected speech in cognitively unimpaired adults
Abstract
Introduction: Connected speech and language (CSL) decline has been associated with early cognitive decline, but associations between CSL and Alzheimer's disease (AD) biomarkers remain a gap in the literature. Our goal was to examine associations with amyloid beta (Aβ) and longitudinal CSL trajectories in cognitively unimpaired adults at increased AD risk.
Methods: Using data from the Wisconsin Registry for Alzheimer's Prevention, CSL measures were automatically extracted from digitally recorded picture descriptions. Positron emission tomography determined Aβ status. Linear mixed effects models assessed the interaction between age and Aβ on CSL trajectories.
Results: Participants who were Aβ positive experienced more rapid decline on specific word content, when controlling for age, sex, and literacy. There were no differences between groups in lexical diversity measures over time.
Discussion: These results indicate that declines in connected speech may be related to preclinical AD. CSL may be a promising, inexpensive, and easy-to-collect digital cognitive marker for AD studies.
Keywords: Alzheimer's disease; Mild Cognitive Impairment; PET imaging; Pittsburgh Compound‐B; speech; computational linguistics; connected speech; dementia; discourse; language; picture description; preclinical Alzheimer's disease.
© 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association.
Conflict of interest statement
Aside from external funding listed in the acknowledgments, no other authors have disclosures to report.
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- R01 AG037639/AG/NIA NIH HHS/United States
- F30 AG054115/AG/NIA NIH HHS/United States
- UL1 TR000427/TR/NCATS NIH HHS/United States
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- T32 GM008692/GM/NIGMS NIH HHS/United States
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- R01 AG062285/AG/NIA NIH HHS/United States
- P30 AG062715/AG/NIA NIH HHS/United States
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