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Coronary artery disease and its impact on the pulsatile brain: A functional NIRS study

Recent studies have reported that optical indices of cerebral pulsatility are associated with cerebrovascular health in older adults. Such indices, including cerebral pulse amplitude and the pulse relaxation function (PRF), have been previously applied to quantify global and regional cerebral pulsat...

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Autores principales: Mohammadi, Hanieh, Vincent, Thomas, Peng, Ke, Nigam, Anil, Gayda, Mathieu, Fraser, Sarah, Joanette, Yves, Lesage, Frédéric, Bherer, Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288102/
https://www.ncbi.nlm.nih.gov/pubmed/33991155
http://dx.doi.org/10.1002/hbm.25463
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author Mohammadi, Hanieh
Vincent, Thomas
Peng, Ke
Nigam, Anil
Gayda, Mathieu
Fraser, Sarah
Joanette, Yves
Lesage, Frédéric
Bherer, Louis
author_facet Mohammadi, Hanieh
Vincent, Thomas
Peng, Ke
Nigam, Anil
Gayda, Mathieu
Fraser, Sarah
Joanette, Yves
Lesage, Frédéric
Bherer, Louis
author_sort Mohammadi, Hanieh
collection PubMed
description Recent studies have reported that optical indices of cerebral pulsatility are associated with cerebrovascular health in older adults. Such indices, including cerebral pulse amplitude and the pulse relaxation function (PRF), have been previously applied to quantify global and regional cerebral pulsatility. The aim of the present study was to determine whether these indices are modulated by cardiovascular status and whether they differ between individuals with low or high cardiovascular risk factors (LCVRF and HCVRF) and coronary artery disease (CAD). A total of 60 older adults aged 57–79 were enrolled in the study. Participants were grouped as LCVRF, HCVRF, and CAD. Participants were asked to walk freely on a gym track while a near‐infrared spectroscopy (NIRS) device recorded hemodynamics data. Low‐intensity, short‐duration walking was used to test whether a brief cardiovascular challenge could increase the difference of pulsatility indices with respect to cardiovascular status. Results indicated that CAD individuals have higher global cerebral pulse amplitude compared with the other groups. Walking reduced global cerebral pulse amplitude and PRF in all groups but did not increase the difference across the groups. Instead, walking extended the spatial distribution of cerebral pulse amplitude to the anterior prefrontal cortex when CAD was compared to the CVRF groups. Further research is needed to determine whether cerebral pulse amplitude extracted from data acquired with NIRS, which is a noninvasive, inexpensive method, can provide an index to characterize the cerebrovascular status associated with CAD.
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spelling pubmed-82881022021-07-21 Coronary artery disease and its impact on the pulsatile brain: A functional NIRS study Mohammadi, Hanieh Vincent, Thomas Peng, Ke Nigam, Anil Gayda, Mathieu Fraser, Sarah Joanette, Yves Lesage, Frédéric Bherer, Louis Hum Brain Mapp Research Articles Recent studies have reported that optical indices of cerebral pulsatility are associated with cerebrovascular health in older adults. Such indices, including cerebral pulse amplitude and the pulse relaxation function (PRF), have been previously applied to quantify global and regional cerebral pulsatility. The aim of the present study was to determine whether these indices are modulated by cardiovascular status and whether they differ between individuals with low or high cardiovascular risk factors (LCVRF and HCVRF) and coronary artery disease (CAD). A total of 60 older adults aged 57–79 were enrolled in the study. Participants were grouped as LCVRF, HCVRF, and CAD. Participants were asked to walk freely on a gym track while a near‐infrared spectroscopy (NIRS) device recorded hemodynamics data. Low‐intensity, short‐duration walking was used to test whether a brief cardiovascular challenge could increase the difference of pulsatility indices with respect to cardiovascular status. Results indicated that CAD individuals have higher global cerebral pulse amplitude compared with the other groups. Walking reduced global cerebral pulse amplitude and PRF in all groups but did not increase the difference across the groups. Instead, walking extended the spatial distribution of cerebral pulse amplitude to the anterior prefrontal cortex when CAD was compared to the CVRF groups. Further research is needed to determine whether cerebral pulse amplitude extracted from data acquired with NIRS, which is a noninvasive, inexpensive method, can provide an index to characterize the cerebrovascular status associated with CAD. John Wiley & Sons, Inc. 2021-05-15 /pmc/articles/PMC8288102/ /pubmed/33991155 http://dx.doi.org/10.1002/hbm.25463 Text en © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Mohammadi, Hanieh
Vincent, Thomas
Peng, Ke
Nigam, Anil
Gayda, Mathieu
Fraser, Sarah
Joanette, Yves
Lesage, Frédéric
Bherer, Louis
Coronary artery disease and its impact on the pulsatile brain: A functional NIRS study
title Coronary artery disease and its impact on the pulsatile brain: A functional NIRS study
title_full Coronary artery disease and its impact on the pulsatile brain: A functional NIRS study
title_fullStr Coronary artery disease and its impact on the pulsatile brain: A functional NIRS study
title_full_unstemmed Coronary artery disease and its impact on the pulsatile brain: A functional NIRS study
title_short Coronary artery disease and its impact on the pulsatile brain: A functional NIRS study
title_sort coronary artery disease and its impact on the pulsatile brain: a functional nirs study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288102/
https://www.ncbi.nlm.nih.gov/pubmed/33991155
http://dx.doi.org/10.1002/hbm.25463
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