학술논문
APOEε4 potentiates amyloid β effects on longitudinal tau pathology
Document Type
Original Paper
Author
Ferrari-Souza, João Pedro; Bellaver, Bruna; Ferreira, Pâmela C. L.; Benedet, Andréa L.; Povala, Guilherme; Lussier, Firoza Z.; Leffa, Douglas T.; Therriault, Joseph; Tissot, Cécile; Soares, Carolina; Wang, Yi-Ting; Chamoun, Mira; Servaes, Stijn; Macedo, Arthur C.; Vermeiren, Marie; Bezgin, Gleb; Kang, Min Su; Stevenson, Jenna; Rahmouni, Nesrine; Pallen, Vanessa; Poltronetti, Nina Margherita; Cohen, Ann; Lopez, Oscar L.; Klunk, William E.; Soucy, Jean-Paul; Gauthier, Serge; Souza, Diogo O.; Triana-Baltzer, Gallen; Saad, Ziad S.; Kolb, Hartmuth C.; Karikari, Thomas K.; Villemagne, Victor L.; Tudorascu, Dana L.; Ashton, Nicholas J.; Zetterberg, Henrik; Blennow, Kaj; Zimmer, Eduardo R.; Rosa-Neto, Pedro; Pascoal, Tharick A.
Source
Nature Aging. 3(10):1210-1218
Subject
Language
English
ISSN
2662-8465
Abstract
The mechanisms by which the apolipoprotein E ε4 (APOEε4) allele influences the pathophysiological progression of Alzheimer’s disease (AD) are poorly understood. Here we tested the association of APOEε4 carriership and amyloid-β (Aβ) burden with longitudinal tau pathology. We longitudinally assessed 94 individuals across the aging and AD spectrum who underwent clinical assessments, APOE genotyping, magnetic resonance imaging, positron emission tomography (PET) for Aβ ([18 F]AZD4694) and tau ([18 F]MK-6240) at baseline, as well as a 2-year follow-up tau-PET scan. We found that APOEε4 carriership potentiates Aβ effects on longitudinal tau accumulation over 2 years. The APOEε4-potentiated Aβ effects on tau-PET burden were mediated by longitudinal plasma phosphorylated tau at threonine 217 (p-tau217+ ) increase. This longitudinal tau accumulation as measured by PET was accompanied by brain atrophy and clinical decline. Our results suggest that the APOEε4 allele plays a key role in Aβ downstream effects on the aggregation of phosphorylated tau in the living human brain.
Ferrari-Souza et al. show that the APOEε4 allele potentiates the deleterious effects of Aβ on the longitudinal accumulation of tau tangles in neocortical brain regions, via tau phosphorylation, which coincides with brain atrophy and clinical decline.
Ferrari-Souza et al. show that the APOEε4 allele potentiates the deleterious effects of Aβ on the longitudinal accumulation of tau tangles in neocortical brain regions, via tau phosphorylation, which coincides with brain atrophy and clinical decline.