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Impact of Amyloid Burden on Regional Functional Synchronization in the Cognitively Normal Older Adults

Previous studies have shown aberrant functional connectivity in preclinical Alzheimer’s disease (AD). However, the effects of beta-amyloid (Aβ) retention on regional functional synchronization in cognitively normal older adults still remain unclear. The aim of this study was to explore the distincti...

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Autores principales: Kang, Dong Woo, Choi, Woo Hee, Jung, Won Sang, Um, Yoo Hyun, Lee, Chang Uk, Lim, Hyun Kook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665874/
https://www.ncbi.nlm.nih.gov/pubmed/29089631
http://dx.doi.org/10.1038/s41598-017-15001-8
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author Kang, Dong Woo
Choi, Woo Hee
Jung, Won Sang
Um, Yoo Hyun
Lee, Chang Uk
Lim, Hyun Kook
author_facet Kang, Dong Woo
Choi, Woo Hee
Jung, Won Sang
Um, Yoo Hyun
Lee, Chang Uk
Lim, Hyun Kook
author_sort Kang, Dong Woo
collection PubMed
description Previous studies have shown aberrant functional connectivity in preclinical Alzheimer’s disease (AD). However, the effects of beta-amyloid (Aβ) retention on regional functional synchronization in cognitively normal older adults still remain unclear. The aim of this study was to explore the distinctive association pattern between Aβ retention and regional functional synchronization in cognitively normal older adults. Sixty-one older adults with normal cognition underwent functional magnetic resonance imaging and regional functional synchronizations were quantified using regional homogeneity (ReHo). Subjects were dichotomized using (18)F-Florbetaben positron emission tomography imaging into subjects with (Aβ+; n = 30) and without (Aβ-; n = 31) Aβ burden. The Aβ+ group exhibited significantly higher ReHo in the fusiform gyrus and lower ReHo in the precuneus compared with the Aβ- group. We found significant negative correlations between global Aβ retention and ReHo in the precuneus and medial prefrontal cortex and positive correlations between global Aβ retention and ReHo in the bilateral lingual gyrus, left fusiform gyrus, and right middle temporal gyrus in the Aβ+ group. Our findings suggest that regional functional synchronization might have distinctive association patterns with Aβ retention in the cognitively normal older adults. These findings can enrich the functional characterization of early stages of disease progression in AD.
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spelling pubmed-56658742017-11-08 Impact of Amyloid Burden on Regional Functional Synchronization in the Cognitively Normal Older Adults Kang, Dong Woo Choi, Woo Hee Jung, Won Sang Um, Yoo Hyun Lee, Chang Uk Lim, Hyun Kook Sci Rep Article Previous studies have shown aberrant functional connectivity in preclinical Alzheimer’s disease (AD). However, the effects of beta-amyloid (Aβ) retention on regional functional synchronization in cognitively normal older adults still remain unclear. The aim of this study was to explore the distinctive association pattern between Aβ retention and regional functional synchronization in cognitively normal older adults. Sixty-one older adults with normal cognition underwent functional magnetic resonance imaging and regional functional synchronizations were quantified using regional homogeneity (ReHo). Subjects were dichotomized using (18)F-Florbetaben positron emission tomography imaging into subjects with (Aβ+; n = 30) and without (Aβ-; n = 31) Aβ burden. The Aβ+ group exhibited significantly higher ReHo in the fusiform gyrus and lower ReHo in the precuneus compared with the Aβ- group. We found significant negative correlations between global Aβ retention and ReHo in the precuneus and medial prefrontal cortex and positive correlations between global Aβ retention and ReHo in the bilateral lingual gyrus, left fusiform gyrus, and right middle temporal gyrus in the Aβ+ group. Our findings suggest that regional functional synchronization might have distinctive association patterns with Aβ retention in the cognitively normal older adults. These findings can enrich the functional characterization of early stages of disease progression in AD. Nature Publishing Group UK 2017-10-31 /pmc/articles/PMC5665874/ /pubmed/29089631 http://dx.doi.org/10.1038/s41598-017-15001-8 Text en © The Author(s) 2017 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/.
spellingShingle Article
Kang, Dong Woo
Choi, Woo Hee
Jung, Won Sang
Um, Yoo Hyun
Lee, Chang Uk
Lim, Hyun Kook
Impact of Amyloid Burden on Regional Functional Synchronization in the Cognitively Normal Older Adults
title Impact of Amyloid Burden on Regional Functional Synchronization in the Cognitively Normal Older Adults
title_full Impact of Amyloid Burden on Regional Functional Synchronization in the Cognitively Normal Older Adults
title_fullStr Impact of Amyloid Burden on Regional Functional Synchronization in the Cognitively Normal Older Adults
title_full_unstemmed Impact of Amyloid Burden on Regional Functional Synchronization in the Cognitively Normal Older Adults
title_short Impact of Amyloid Burden on Regional Functional Synchronization in the Cognitively Normal Older Adults
title_sort impact of amyloid burden on regional functional synchronization in the cognitively normal older adults
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665874/
https://www.ncbi.nlm.nih.gov/pubmed/29089631
http://dx.doi.org/10.1038/s41598-017-15001-8
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