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Greater BOLD Variability is Associated With Poorer Cognitive Function in an Adult Lifespan Sample

Moment-to-moment fluctuations in brain signal assessed by functional magnetic resonance imaging blood oxygenation level dependent (BOLD) variability is increasingly thought to represent important “signal” rather than measurement-related “noise.” Efforts to characterize BOLD variability in healthy ag...

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Autores principales: Boylan, Maria A, Foster, Chris M, Pongpipat, Ekarin E, Webb, Christina E, Rodrigue, Karen M, Kennedy, Kristen M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727366/
https://www.ncbi.nlm.nih.gov/pubmed/32915200
http://dx.doi.org/10.1093/cercor/bhaa243
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author Boylan, Maria A
Foster, Chris M
Pongpipat, Ekarin E
Webb, Christina E
Rodrigue, Karen M
Kennedy, Kristen M
author_facet Boylan, Maria A
Foster, Chris M
Pongpipat, Ekarin E
Webb, Christina E
Rodrigue, Karen M
Kennedy, Kristen M
author_sort Boylan, Maria A
collection PubMed
description Moment-to-moment fluctuations in brain signal assessed by functional magnetic resonance imaging blood oxygenation level dependent (BOLD) variability is increasingly thought to represent important “signal” rather than measurement-related “noise.” Efforts to characterize BOLD variability in healthy aging have yielded mixed outcomes, demonstrating both age-related increases and decreases in BOLD variability and both detrimental and beneficial associations. Utilizing BOLD mean-squared-successive-differences (MSSD) during a digit n-back working memory (WM) task in a sample of healthy adults (aged 20–94 years; n = 171), we examined effects of aging on whole-brain 1) BOLD variability during task (mean condition MSSD across 0–2–3-4 back conditions), 2) BOLD variability modulation to incrementally increasing WM difficulty (linear slope from 0–2–3-4 back), and 3) the association of age-related differences in variability with in- and out-of-scanner WM performance. Widespread cortical and subcortical regions evidenced increased mean variability with increasing age, with no regions evidencing age-related decrease in variability. Additionally, posterior cingulate/precuneus exhibited increased variability to WM difficulty. Notably, both age-related increases in BOLD variability were associated with significantly poorer WM performance in all but the oldest adults. These findings lend support to the growing corpus suggesting that brain-signal variability is altered in healthy aging; specifically, in this adult lifespan sample, BOLD-variability increased with age and was detrimental to cognitive performance.
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spelling pubmed-77273662020-12-16 Greater BOLD Variability is Associated With Poorer Cognitive Function in an Adult Lifespan Sample Boylan, Maria A Foster, Chris M Pongpipat, Ekarin E Webb, Christina E Rodrigue, Karen M Kennedy, Kristen M Cereb Cortex Original Article Moment-to-moment fluctuations in brain signal assessed by functional magnetic resonance imaging blood oxygenation level dependent (BOLD) variability is increasingly thought to represent important “signal” rather than measurement-related “noise.” Efforts to characterize BOLD variability in healthy aging have yielded mixed outcomes, demonstrating both age-related increases and decreases in BOLD variability and both detrimental and beneficial associations. Utilizing BOLD mean-squared-successive-differences (MSSD) during a digit n-back working memory (WM) task in a sample of healthy adults (aged 20–94 years; n = 171), we examined effects of aging on whole-brain 1) BOLD variability during task (mean condition MSSD across 0–2–3-4 back conditions), 2) BOLD variability modulation to incrementally increasing WM difficulty (linear slope from 0–2–3-4 back), and 3) the association of age-related differences in variability with in- and out-of-scanner WM performance. Widespread cortical and subcortical regions evidenced increased mean variability with increasing age, with no regions evidencing age-related decrease in variability. Additionally, posterior cingulate/precuneus exhibited increased variability to WM difficulty. Notably, both age-related increases in BOLD variability were associated with significantly poorer WM performance in all but the oldest adults. These findings lend support to the growing corpus suggesting that brain-signal variability is altered in healthy aging; specifically, in this adult lifespan sample, BOLD-variability increased with age and was detrimental to cognitive performance. Oxford University Press 2020-09-11 /pmc/articles/PMC7727366/ /pubmed/32915200 http://dx.doi.org/10.1093/cercor/bhaa243 Text en © The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Boylan, Maria A
Foster, Chris M
Pongpipat, Ekarin E
Webb, Christina E
Rodrigue, Karen M
Kennedy, Kristen M
Greater BOLD Variability is Associated With Poorer Cognitive Function in an Adult Lifespan Sample
title Greater BOLD Variability is Associated With Poorer Cognitive Function in an Adult Lifespan Sample
title_full Greater BOLD Variability is Associated With Poorer Cognitive Function in an Adult Lifespan Sample
title_fullStr Greater BOLD Variability is Associated With Poorer Cognitive Function in an Adult Lifespan Sample
title_full_unstemmed Greater BOLD Variability is Associated With Poorer Cognitive Function in an Adult Lifespan Sample
title_short Greater BOLD Variability is Associated With Poorer Cognitive Function in an Adult Lifespan Sample
title_sort greater bold variability is associated with poorer cognitive function in an adult lifespan sample
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727366/
https://www.ncbi.nlm.nih.gov/pubmed/32915200
http://dx.doi.org/10.1093/cercor/bhaa243
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