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Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging
Cognitive decline is a major biomedical challenge as the global population ages. Elevated levels of the longevity factor klotho suppress aging, enhance cognition, and promote synaptic plasticity and neural resilience against aging and Alzheimer’s disease (AD)-related pathogenic proteins. Here, we ex...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382127/ https://www.ncbi.nlm.nih.gov/pubmed/27714549 http://dx.doi.org/10.1007/s11682-016-9598-2 |
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author | Yokoyama, Jennifer S. Marx, Gabe Brown, Jesse A. Bonham, Luke W. Wang, Dan Coppola, Giovanni Seeley, William W. Rosen, Howard J. Miller, Bruce L. Kramer, Joel H. Dubal, Dena B. |
author_facet | Yokoyama, Jennifer S. Marx, Gabe Brown, Jesse A. Bonham, Luke W. Wang, Dan Coppola, Giovanni Seeley, William W. Rosen, Howard J. Miller, Bruce L. Kramer, Joel H. Dubal, Dena B. |
author_sort | Yokoyama, Jennifer S. |
collection | PubMed |
description | Cognitive decline is a major biomedical challenge as the global population ages. Elevated levels of the longevity factor klotho suppress aging, enhance cognition, and promote synaptic plasticity and neural resilience against aging and Alzheimer’s disease (AD)-related pathogenic proteins. Here, we examined the relationship between human genetic variants of KLOTHO and systemic klotho levels – and assessed neuroanatomic correlates of serum klotho in a cohort of healthy older adults. Serum klotho levels were increased with KL-VS heterozygosity, as anticipated. We report, for the first time, that serum klotho levels were paradoxically decreased with KL-VS homozygosity. Further, we found that higher serum klotho levels were associated with measures of greater intrinsic connectivity in key functional networks of the brain vulnerable to aging and AD such as the fronto-parietal and default mode networks. Our findings suggest that elevated klotho promotes a resilient brain, possibly through increased network connectivity of critical brain regions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11682-016-9598-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5382127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-53821272017-04-28 Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging Yokoyama, Jennifer S. Marx, Gabe Brown, Jesse A. Bonham, Luke W. Wang, Dan Coppola, Giovanni Seeley, William W. Rosen, Howard J. Miller, Bruce L. Kramer, Joel H. Dubal, Dena B. Brain Imaging Behav SI: Resilience/Reserve in AD Cognitive decline is a major biomedical challenge as the global population ages. Elevated levels of the longevity factor klotho suppress aging, enhance cognition, and promote synaptic plasticity and neural resilience against aging and Alzheimer’s disease (AD)-related pathogenic proteins. Here, we examined the relationship between human genetic variants of KLOTHO and systemic klotho levels – and assessed neuroanatomic correlates of serum klotho in a cohort of healthy older adults. Serum klotho levels were increased with KL-VS heterozygosity, as anticipated. We report, for the first time, that serum klotho levels were paradoxically decreased with KL-VS homozygosity. Further, we found that higher serum klotho levels were associated with measures of greater intrinsic connectivity in key functional networks of the brain vulnerable to aging and AD such as the fronto-parietal and default mode networks. Our findings suggest that elevated klotho promotes a resilient brain, possibly through increased network connectivity of critical brain regions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11682-016-9598-2) contains supplementary material, which is available to authorized users. Springer US 2016-10-06 2017 /pmc/articles/PMC5382127/ /pubmed/27714549 http://dx.doi.org/10.1007/s11682-016-9598-2 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | SI: Resilience/Reserve in AD Yokoyama, Jennifer S. Marx, Gabe Brown, Jesse A. Bonham, Luke W. Wang, Dan Coppola, Giovanni Seeley, William W. Rosen, Howard J. Miller, Bruce L. Kramer, Joel H. Dubal, Dena B. Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging |
title | Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging |
title_full | Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging |
title_fullStr | Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging |
title_full_unstemmed | Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging |
title_short | Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging |
title_sort | systemic klotho is associated with klotho variation and predicts intrinsic cortical connectivity in healthy human aging |
topic | SI: Resilience/Reserve in AD |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382127/ https://www.ncbi.nlm.nih.gov/pubmed/27714549 http://dx.doi.org/10.1007/s11682-016-9598-2 |
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