Plasma phosphorylated tau181 outperforms [<scp><sup>18</sup>F</scp>] <scp>fluorodeoxyglucose positron emission tomography</scp> in the identification of early Alzheimer disease

Overall, although both plasma p-tau181 and [<sup>18</sup>F]FDG-PET were associated with core AD biomarkers, plasma p-tau181 outperformed [<sup>18</sup>F]FDG-PET in identifying individuals with early AD pathophysiology. Taken together, our study suggests that plasma p-tau181 may aid in detecting individuals with underlying early AD.

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Publication Details

Journal
European Journal of Neurology
Published
2024-10-24
DOI
https://doi.org/10.1111/ene.16255
Citations
7
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
2.70

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article

Plasma phosphorylated tau181 outperforms [18F] fluorodeoxyglucose positron emission tomography in the identification of early Alzheimer disease

Serge Gauthier, Bertrand J. Jean‐Claude, Tharick Ali Pascoal, Joseph Therriault et al.
7 citations
European Journal of Neurology
Dementia and Cognitive Impairment Research
2.70
article

Plasma phosphorylated tau181 outperforms [18F] fluorodeoxyglucose positron emission tomography in the identification of early Alzheimer disease

Serge Gauthier, Bertrand J. Jean‐Claude, Tharick Ali Pascoal, Joseph Therriault, Nicholas James Ashton, Eduardo Rigon Zimmer, Brian M. Gilfix, Kaj Blennow, Jean‐Paul Soucy, Jaime Fernández Arias, Nesrine Rahmouni, Andréa Lessa Benedet, Arthur C. Macedo, Thomas K. Karikari, Seyyed Ali Hosseini, Stijn Servaes, Takashi Matsudaira, Firoza Zubeida Lussier, Cécile Tissot, Kely Quispialaya, Henrik Zetterberg, Pedro Rosa‐Neto, Yi‐Ting Wang, Jenna Stevenson, Antonio Aliaga
article en
7 citations

Abstract

Overall, although both plasma p-tau181 and [<sup>18</sup>F]FDG-PET were associated with core AD biomarkers, plasma p-tau181 outperformed [<sup>18</sup>F]FDG-PET in identifying individuals with early AD pathophysiology. Taken together, our study suggests that plasma p-tau181 may aid in detecting individuals with underlying early AD.

European Journal of NeurologyVol. 31(12)
Montreal Neurological Institute and Hospital (CA), Universidade Federal do Rio Grande do Sul (BR), University of Pittsburgh (US), Douglas Mental Health University Institute (CA), Sahlgrenska University Hospital (SE), Hamamatsu University School of Medicine (JP), National Epilepsy Center (JP), Wallenberg Wood Science Center (SE), UK Dementia Research Institute (GB), National Hospital Organization (JP), University College London (GB), Pontifícia Universidade Católica do Rio Grande do Sul (BR), McGill University (CA), University of Gothenburg (SE)
U.S. Department of Defense, Alzheimer's Association, Bristol-Myers Squibb, Eli Lilly and Company, Biogen, University of Southern California, F. Hoffmann-La Roche, Alzheimer's Disease Neuroimaging Initiative, Familjen Erling-Perssons Stiftelse, BioClinica, McGill University, Fondation Brain Canada, Northern California Institute for Research and Education, Stiftelsen för Gamla Tjänarinnor, Weston Brain Institute, EU Joint Programme – Neurodegenerative Disease Research, Consortium canadien en neurodégénérescence associée au vieillissement, National Institute for Health and Care Research, University College London, European Commission, Eisai, Hjärnfonden, Vetenskapsrådet, UK Dementia Research Institute, National Institutes of Health, Genentech, University of California, San Diego, HORIZON EUROPE Framework Programme, Canadian Institutes of Health Research, Fonds de Recherche du Québec - Santé
Good health and well-being
Openalex Percentile: Top 9%
Dementia and Cognitive Impairment Research
2.70
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