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Impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7T MRI

Arterial walls stiffen with age, cardiovascular risk factors, and various vascular diseases, which may lead to less damping of the arterial blood flow pulse, subsequent microvascular damage, and enlarged perivascular spaces (PVS). However, the exact interplay between these processes is unclear. This...

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Autores principales: van den Kerkhof, Marieke, van der Thiel, Merel M, van Oostenbrugge, Robert J, Postma, Alida A, Kroon, Abraham A, Backes, Walter H, Jansen, Jacobus FA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196747/
https://www.ncbi.nlm.nih.gov/pubmed/36704826
http://dx.doi.org/10.1177/0271678X231153374
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author van den Kerkhof, Marieke
van der Thiel, Merel M
van Oostenbrugge, Robert J
Postma, Alida A
Kroon, Abraham A
Backes, Walter H
Jansen, Jacobus FA
author_facet van den Kerkhof, Marieke
van der Thiel, Merel M
van Oostenbrugge, Robert J
Postma, Alida A
Kroon, Abraham A
Backes, Walter H
Jansen, Jacobus FA
author_sort van den Kerkhof, Marieke
collection PubMed
description Arterial walls stiffen with age, cardiovascular risk factors, and various vascular diseases, which may lead to less damping of the arterial blood flow pulse, subsequent microvascular damage, and enlarged perivascular spaces (PVS). However, the exact interplay between these processes is unclear. This study aimed to investigate the relation between blood flow velocity pulsatility in the small lenticulostriate arteries and their supplying middle cerebral artery and the respective damping factor (DF), with the number of MRI-visible PVS in elderly subjects. Blood flow velocity waveforms were obtained in 45 subjects (median age [range]: 64 [48–81] years, 47% male) using 7T MRI. PVS were scored in the basal ganglia (BG) and centrum semiovale (CSO). Spearman correlation analyses were used to determine associations of the blood flow pulsatility and the DF, with PVS score, adjusted for age and sex. We found a significant association between a lower DF and a higher number of PVS in the BG (r(s) = −0.352, P = 0.021), but not in the CSO. This finding supports the supposed pathophysiological mechanism in which excessive kinetic energy deposition leads to damage of small perforating arteries and contributes to the enlargement of PVS at the level of the BG, but possible other pathways might also be of influence.
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spelling pubmed-101967472023-05-20 Impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7T MRI van den Kerkhof, Marieke van der Thiel, Merel M van Oostenbrugge, Robert J Postma, Alida A Kroon, Abraham A Backes, Walter H Jansen, Jacobus FA J Cereb Blood Flow Metab Original Articles Arterial walls stiffen with age, cardiovascular risk factors, and various vascular diseases, which may lead to less damping of the arterial blood flow pulse, subsequent microvascular damage, and enlarged perivascular spaces (PVS). However, the exact interplay between these processes is unclear. This study aimed to investigate the relation between blood flow velocity pulsatility in the small lenticulostriate arteries and their supplying middle cerebral artery and the respective damping factor (DF), with the number of MRI-visible PVS in elderly subjects. Blood flow velocity waveforms were obtained in 45 subjects (median age [range]: 64 [48–81] years, 47% male) using 7T MRI. PVS were scored in the basal ganglia (BG) and centrum semiovale (CSO). Spearman correlation analyses were used to determine associations of the blood flow pulsatility and the DF, with PVS score, adjusted for age and sex. We found a significant association between a lower DF and a higher number of PVS in the BG (r(s) = −0.352, P = 0.021), but not in the CSO. This finding supports the supposed pathophysiological mechanism in which excessive kinetic energy deposition leads to damage of small perforating arteries and contributes to the enlargement of PVS at the level of the BG, but possible other pathways might also be of influence. SAGE Publications 2023-01-26 2023-06 /pmc/articles/PMC10196747/ /pubmed/36704826 http://dx.doi.org/10.1177/0271678X231153374 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
van den Kerkhof, Marieke
van der Thiel, Merel M
van Oostenbrugge, Robert J
Postma, Alida A
Kroon, Abraham A
Backes, Walter H
Jansen, Jacobus FA
Impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7T MRI
title Impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7T MRI
title_full Impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7T MRI
title_fullStr Impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7T MRI
title_full_unstemmed Impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7T MRI
title_short Impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7T MRI
title_sort impaired damping of cerebral blood flow velocity pulsatility is associated with the number of perivascular spaces as measured with 7t mri
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196747/
https://www.ncbi.nlm.nih.gov/pubmed/36704826
http://dx.doi.org/10.1177/0271678X231153374
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