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KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease

Klotho-VS heterozygosity (KL-VS(het)) is associated with reduced risk of Alzheimer’s disease (AD). However, whether KL-VS(het) is associated with lower levels of pathologic tau, i.e., the key AD pathology driving neurodegeneration and cognitive decline, is unknown. Here, we assessed the interaction...

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Detalles Bibliográficos
Autores principales: Neitzel, Julia, Franzmeier, Nicolai, Rubinski, Anna, Dichgans, Martin, Brendel, Matthias, Malik, Rainer, Ewers, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219708/
https://www.ncbi.nlm.nih.gov/pubmed/34158479
http://dx.doi.org/10.1038/s41467-021-23755-z
Descripción
Sumario:Klotho-VS heterozygosity (KL-VS(het)) is associated with reduced risk of Alzheimer’s disease (AD). However, whether KL-VS(het) is associated with lower levels of pathologic tau, i.e., the key AD pathology driving neurodegeneration and cognitive decline, is unknown. Here, we assessed the interaction between KL-VS(het) and levels of beta-amyloid, a key driver of tau pathology, on the levels of PET-assessed neurofibrillary tau in 551 controls and patients across the AD continuum. KL-VS(het) showed lower cross-sectional and longitudinal increase in tau-PET per unit increase in amyloid-PET when compared to that of non-carriers. This association of KL-VS(het) on tau-PET was stronger in Klotho mRNA-expressing brain regions mapped onto a gene expression atlas. KL-VS(het) was related to better memory functions in amyloid-positive participants and this association was mediated by lower tau-PET. Amyloid-PET levels did not differ between KL-VS(het) carriers versus non-carriers. Together, our findings provide evidence to suggest a protective role of KL-VS(het) against amyloid-related tau pathology and tau-related memory impairments in elderly humans at risk of AD dementia.