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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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 |
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author | Neitzel, Julia Franzmeier, Nicolai Rubinski, Anna Dichgans, Martin Brendel, Matthias Malik, Rainer Ewers, Michael |
author_facet | Neitzel, Julia Franzmeier, Nicolai Rubinski, Anna Dichgans, Martin Brendel, Matthias Malik, Rainer Ewers, Michael |
author_sort | Neitzel, Julia |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8219708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82197082021-07-09 KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease Neitzel, Julia Franzmeier, Nicolai Rubinski, Anna Dichgans, Martin Brendel, Matthias Malik, Rainer Ewers, Michael Nat Commun Article 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. Nature Publishing Group UK 2021-06-22 /pmc/articles/PMC8219708/ /pubmed/34158479 http://dx.doi.org/10.1038/s41467-021-23755-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Neitzel, Julia Franzmeier, Nicolai Rubinski, Anna Dichgans, Martin Brendel, Matthias Malik, Rainer Ewers, Michael KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease |
title | KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease |
title_full | KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease |
title_fullStr | KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease |
title_full_unstemmed | KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease |
title_short | KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease |
title_sort | kl-vs heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in alzheimer’s disease |
topic | Article |
url | 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 |
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