Spatial proteomic differences in chronic traumatic encephalopathy, Alzheimer's disease, and primary age‐related tauopathy hippocampi

Alzheimer's disease neuropathologic change (ADNC), possible primary age-related tauopathy (PART), definite PART, and chronic traumatic encephalopathy (CTE) can be differentiated based on the proteomic composition of their neurofibrillary tangle (NFT)- and non-NFT-bearing neurons. The proteome of these NFT- and non-NFT-bearing neurons is largely correlated with the presence or absence of amyloid beta (Aβ). Neurons in CTE and definite PART (Aβ-independent pathologies) share numerous proteomic similarities that distinguish them from ADNC and possible PART (Aβ-positive pathologies).

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-31
DOI
https://doi.org/10.1002/alz.14487
Citations
4
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
1.31

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article

Spatial proteomic differences in chronic traumatic encephalopathy, Alzheimer's disease, and primary age‐related tauopathy hippocampi

Justin Kauffman, Susan K. Rohde, Kevin Clare, Elena V. Daoud et al.
4 citations
Alzheimer s & Dementia
Alzheimer's disease research and treatments
1.31
article

Spatial proteomic differences in chronic traumatic encephalopathy, Alzheimer's disease, and primary age‐related tauopathy hippocampi

Justin Kauffman, Susan K. Rohde, Kevin Clare, Elena V. Daoud, Kevin F. Bieniek, Carolina Maldonado‐Díaz, Charles L. White, Kurt Farrell, Adam O. Goldstein, Enna Selmanovic, Thor D. Stein, Emma L Thorn, Ann Carolyn McKee, Tiffany F. Kautz, Miranda E. Orr, Connie Slocum, Leyla Canbeldek, Thomas Wısnıewskı, Michael L. Alosco, Daniel Koenigsberg, Timothy E. Richardson, Satomi Hiya, Eleanor Drummond, John F. Crary, Lakshmi Shree Kulumani Mahadevan, Gabriel A. Marx, Jorge Samanamud, Jamie M. Walker, Alexander J. Ehrenberg, Timothy C. Orr, Alison Goate, Raquel T. Yokoda, Jesse Mez, Claudia De Sanctis, Nicholas Scibetta, Robina Afzal, Thomas D. Christie, Victoria Flores‐Almazan
article en
4 citations

Abstract

Alzheimer's disease neuropathologic change (ADNC), possible primary age-related tauopathy (PART), definite PART, and chronic traumatic encephalopathy (CTE) can be differentiated based on the proteomic composition of their neurofibrillary tangle (NFT)- and non-NFT-bearing neurons. The proteome of these NFT- and non-NFT-bearing neurons is largely correlated with the presence or absence of amyloid beta (Aβ). Neurons in CTE and definite PART (Aβ-independent pathologies) share numerous proteomic similarities that distinguish them from ADNC and possible PART (Aβ-positive pathologies).

Alzheimer s & DementiaVol. 21(2)
Boston University (US), The University of Sydney (AU), Albert Einstein College of Medicine (US), Allen Institute for Brain Science (US), Montefiore Medical Center (US), The University of Texas at San Antonio Health Science Center (US), University of California, San Francisco (US), Washington University in St. Louis (US), VA Boston Healthcare System (US), VA New England Healthcare System (US), St. Louis VA Medical Center (US), University Memory and Aging Center (US), Amsterdam Neuroscience (NL), Innovative Genomics Institute (US), Institute for Neurodegenerative Disorders (US), New York University (US), Vrije Universiteit Amsterdam (NL), The University of Texas Southwestern Medical Center (US), University of California, Berkeley (US), Icahn School of Medicine at Mount Sinai (US)
U.S. Department of Veterans Affairs, Parkinson's Disease Foundation, Cure Alzheimer's Fund, Rainwater Charitable Foundation, Texas Alzheimer's Research and Care Consortium, National Institutes of Health, National Institute on Aging, National Institute of Neurological Disorders and Stroke
Good health and well-being
Openalex Percentile: Top 18%
Alzheimer's disease research and treatments
1.31
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