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Application of the ATN classification scheme in a population without dementia: Findings from the EPAD cohort

BACKGROUND: We classified non‐demented European Prevention of Alzheimer's Dementia (EPAD) participants through the amyloid/tau/neurodegeneration (ATN) scheme and assessed their neuropsychological and imaging profiles. MATERIALS AND METHODS: From 1500 EPAD participants, 312 were excluded. Cerebr...

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Detalles Bibliográficos
Autores principales: Ingala, Silvia, De Boer, Casper, Masselink, Larissa A, Vergari, Ilaria, Lorenzini, Luigi, Blennow, Kaj, Chételat, Gaël, Di Perri, Carol, Ewers, Michael, van der Flier, Wiesje M, Fox, Nick C, Gispert, Juan Domingo, Haller, Sven, Molinuevo, José Luís, Muniz‐Terrera, Graciela, Mutsaerts, Henri JMM, Ritchie, Craig W, Ritchie, Karen, Schmidt, Mark, Schwarz, Adam J, Vermunt, Lisa, Waldman, Adam D, Wardlaw, Joanna, Wink, Alle Meije, Wolz, Robin, Wottschel, Viktor, Scheltens, Philip, Visser, Pieter Jelle, Barkhof, Frederik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359976/
https://www.ncbi.nlm.nih.gov/pubmed/33811742
http://dx.doi.org/10.1002/alz.12292
Descripción
Sumario:BACKGROUND: We classified non‐demented European Prevention of Alzheimer's Dementia (EPAD) participants through the amyloid/tau/neurodegeneration (ATN) scheme and assessed their neuropsychological and imaging profiles. MATERIALS AND METHODS: From 1500 EPAD participants, 312 were excluded. Cerebrospinal fluid cut‐offs of 1000 pg/mL for amyloid beta (Aß)1‐42 and 27 pg/mL for p‐tau181 were validated using Gaussian mixture models. Given strong correlation of p‐tau and t‐tau (R(2) = 0.98, P < 0.001), neurodegeneration was defined by age‐adjusted hippocampal volume. Multinomial regressions were used to test whether neuropsychological tests and regional brain volumes could distinguish ATN stages. RESULTS: Age was 65 ± 7 years, with 58% females and 38% apolipoprotein E (APOE) ε4 carriers; 57.1% were A–T–N–, 32.5% were in the Alzheimer's disease (AD) continuum, and 10.4% suspected non‐Alzheimer's pathology. Age and cerebrovascular burden progressed with biomarker positivity (P < 0.001). Cognitive dysfunction appeared with T+. Paradoxically higher regional gray matter volumes were observed in A+T–N– compared to A–T–N– (P < 0.001). DISCUSSION: In non‐demented individuals along the AD continuum, p‐tau drives cognitive dysfunction. Memory and language domains are affected in the earliest stages.