Informing etiological heterogeneity of mild cognitive impairment and risk for progression to dementia with plasma p-tau217

MCI is etiologically heterogeneous. The presence of Alzheimer's pathology defined by elevated plasma p-tau217 in individuals with MCI significantly worsens prognosis. Neuropsychiatric symptoms may contribute to cognitive complaints and risk for progressive decline irrespective of AD pathology. Plasma p-tau217 can inform our understanding of base rates of different MCI phenotypes on a larger scale. As with other AD biomarkers, frequency of elevated plasma p-tau217 and odds of progression to dementia requires careful consideration of recruitment source (clinic- vs. community-based), especially across ethno-racially diverse older adults. Ongoing integration of emerging neurodegenerative disease biomarkers with detailed clinical evaluations will continue to improve treatment specificity and prognosis.

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Publication Details

Journal
The Journal of Prevention of Alzheimer s Disease
Published
2025-01-01
DOI
https://doi.org/10.1016/j.tjpad.2024.100011
Citations
9
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
13.24

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article

Informing etiological heterogeneity of mild cognitive impairment and risk for progression to dementia with plasma p-tau217

Franchesca Arias, Warren Barker, Breton M. Asken, David E. Vaillancourt et al.
9 citations
The Journal of Prevention of Alzheimer s Disease
Dementia and Cognitive Impairment Research
13.24
article

Informing etiological heterogeneity of mild cognitive impairment and risk for progression to dementia with plasma p-tau217

Franchesca Arias, Warren Barker, Breton M. Asken, David E. Vaillancourt, Rosie E. Curiel, Idaly Vélez Uribe, Melissa J. Armstrong, Emily F. Matusz, Mónica Rosselli, Michael Marsiske, Wei‐en Wang, Shellie‐Anne Levy, Jesse C. DeSimone, Elizabeth Crocco, Glenn E. Smith, Jacob Fiala, David Loewenstein, Steven T. DeKosky, Ranjan Duara
article en
9 citations

Abstract

MCI is etiologically heterogeneous. The presence of Alzheimer's pathology defined by elevated plasma p-tau217 in individuals with MCI significantly worsens prognosis. Neuropsychiatric symptoms may contribute to cognitive complaints and risk for progressive decline irrespective of AD pathology. Plasma p-tau217 can inform our understanding of base rates of different MCI phenotypes on a larger scale. As with other AD biomarkers, frequency of elevated plasma p-tau217 and odds of progression to dementia requires careful consideration of recruitment source (clinic- vs. community-based), especially across ethno-racially diverse older adults. Ongoing integration of emerging neurodegenerative disease biomarkers with detailed clinical evaluations will continue to improve treatment specificity and prognosis.

The Journal of Prevention of Alzheimer s DiseaseVol. 12(1)
University of Miami (US), Atlantic University (US), University of Florida Health (US), University of Florida (US), Alzheimer’s Disease Neuroimaging Initiative (US), Florida Atlantic University (US)
Biogen, National Institutes of Health, National Institute on Aging
Openalex Percentile: Top 1%
Dementia and Cognitive Impairment Research
13.24
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