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Early detection of microstructural white matter changes associated with arterial pulsatility

Increased cerebral blood flow pulsatility is common in vascular dementia and is associated with macrostructural damage to cerebral white matter or leukoaraiosis (LA). In this study, we examine whether cerebral blood flow pulsatility is associated with macrostructural and microstructural changes in c...

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Autores principales: Jolly, Todd A. D., Bateman, Grant A., Levi, Christopher R., Parsons, Mark W., Michie, Patricia T., Karayanidis, Frini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3831342/
https://www.ncbi.nlm.nih.gov/pubmed/24302906
http://dx.doi.org/10.3389/fnhum.2013.00782
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author Jolly, Todd A. D.
Bateman, Grant A.
Levi, Christopher R.
Parsons, Mark W.
Michie, Patricia T.
Karayanidis, Frini
author_facet Jolly, Todd A. D.
Bateman, Grant A.
Levi, Christopher R.
Parsons, Mark W.
Michie, Patricia T.
Karayanidis, Frini
author_sort Jolly, Todd A. D.
collection PubMed
description Increased cerebral blood flow pulsatility is common in vascular dementia and is associated with macrostructural damage to cerebral white matter or leukoaraiosis (LA). In this study, we examine whether cerebral blood flow pulsatility is associated with macrostructural and microstructural changes in cerebral white matter in older adults with no or mild LA and no evidence of dementia. Diffusion Tensor Imaging was used to measure fractional anisotropy (FA), an index of the microstructural integrity of white matter, and radial diffusivity (RaD), a measure sensitive to the integrity of myelin. When controlling for age, increased arterial pulsation was associated with deterioration in both measures of white matter microstructure but not LA severity. A stepwise multiple linear regression model revealed that arterial pulsatility index was the strongest predictor of FA (R = 0.483, adjusted R(2) = 0.220), followed by LA severity, but not age. These findings suggest that arterial pulsatility may provide insight into age-related reduction in white matter FA. Specifically, increased arterial pulsatility may increase perivascular shear stress and lead to accumulation of damage to perivascular oligodendrocytes, resulting in microstructural changes in white matter and contributing to proliferation of LA over time. Changes in cerebral blood flow pulsatility may therefore provide a sensitive index of white matter health that could facilitate the early detection of risk for perivascular white matter damage and the assessment of the effectiveness of preventative treatment targeted at reducing pulsatility.
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spelling pubmed-38313422013-12-03 Early detection of microstructural white matter changes associated with arterial pulsatility Jolly, Todd A. D. Bateman, Grant A. Levi, Christopher R. Parsons, Mark W. Michie, Patricia T. Karayanidis, Frini Front Hum Neurosci Neuroscience Increased cerebral blood flow pulsatility is common in vascular dementia and is associated with macrostructural damage to cerebral white matter or leukoaraiosis (LA). In this study, we examine whether cerebral blood flow pulsatility is associated with macrostructural and microstructural changes in cerebral white matter in older adults with no or mild LA and no evidence of dementia. Diffusion Tensor Imaging was used to measure fractional anisotropy (FA), an index of the microstructural integrity of white matter, and radial diffusivity (RaD), a measure sensitive to the integrity of myelin. When controlling for age, increased arterial pulsation was associated with deterioration in both measures of white matter microstructure but not LA severity. A stepwise multiple linear regression model revealed that arterial pulsatility index was the strongest predictor of FA (R = 0.483, adjusted R(2) = 0.220), followed by LA severity, but not age. These findings suggest that arterial pulsatility may provide insight into age-related reduction in white matter FA. Specifically, increased arterial pulsatility may increase perivascular shear stress and lead to accumulation of damage to perivascular oligodendrocytes, resulting in microstructural changes in white matter and contributing to proliferation of LA over time. Changes in cerebral blood flow pulsatility may therefore provide a sensitive index of white matter health that could facilitate the early detection of risk for perivascular white matter damage and the assessment of the effectiveness of preventative treatment targeted at reducing pulsatility. Frontiers Media S.A. 2013-11-18 /pmc/articles/PMC3831342/ /pubmed/24302906 http://dx.doi.org/10.3389/fnhum.2013.00782 Text en Copyright © 2013 Jolly, Bateman, Levi, Parsons, Michie and Karayanidis. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Jolly, Todd A. D.
Bateman, Grant A.
Levi, Christopher R.
Parsons, Mark W.
Michie, Patricia T.
Karayanidis, Frini
Early detection of microstructural white matter changes associated with arterial pulsatility
title Early detection of microstructural white matter changes associated with arterial pulsatility
title_full Early detection of microstructural white matter changes associated with arterial pulsatility
title_fullStr Early detection of microstructural white matter changes associated with arterial pulsatility
title_full_unstemmed Early detection of microstructural white matter changes associated with arterial pulsatility
title_short Early detection of microstructural white matter changes associated with arterial pulsatility
title_sort early detection of microstructural white matter changes associated with arterial pulsatility
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3831342/
https://www.ncbi.nlm.nih.gov/pubmed/24302906
http://dx.doi.org/10.3389/fnhum.2013.00782
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