Associations between plasma pTau217, cognitive impairment, and synaptic density in AD vulnerable brain regions

The unexpected directional relationship between pTau217 and synaptic density in the medial temporal lobe could be due to an early compensatory response to pathology accumulation since most individuals in this sample were cognitively unimpaired. Longitudinal studies are forthcoming to determine the trajectory of plasma pTau217 and synaptic density.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70856_103318
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
0.00
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Associations between plasma pTau217, cognitive impairment, and synaptic density in AD vulnerable brain regions

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Associations between plasma pTau217, cognitive impairment, and synaptic density in AD vulnerable brain regions

Randall S. Johnson, Tobey J. Betthauser, Todd E. Barnhart, Erin M. Jonaitis, Rachael E. Wilson, Yazan Hammad‎, Alexandra H DiFilippo, Mary‐Elizabeth Pasquesi, Kao Lee Yang, Bradley T Christian, Jonathan Engle, Henrik Zetterberg, Yue Ma, Nicholas Ashton, Barbara B. Bendlin
article en

Abstract

The unexpected directional relationship between pTau217 and synaptic density in the medial temporal lobe could be due to an early compensatory response to pathology accumulation since most individuals in this sample were cognitively unimpaired. Longitudinal studies are forthcoming to determine the trajectory of plasma pTau217 and synaptic density.

Alzheimer s & DementiaVol. 21(S2)
University of Wisconsin–Madison (US), Hong Kong Science and Technology Parks Corporation (HK), Geriatric Research Education and Clinical Center (US), UK Dementia Research Institute (GB), University of Wisconsin Health (US), William S. Middleton Memorial Veterans Hospital (US), Wisconsin Division of Public Health (US), National Hospital for Neurology and Neurosurgery (GB), University College London (GB), University of Gothenburg (SE)
Openalex Percentile: Top 33%
Alzheimer's disease research and treatments
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