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An investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation()
Cognitive function decline secondary to cardiovascular disease has been reported. However, little is known about the impact of coronary artery disease (CAD) on the aging brain macrostructure or whether exercise training, in the context of cardiovascular rehabilitation, can affect brain structure fol...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814972/ https://www.ncbi.nlm.nih.gov/pubmed/24273722 http://dx.doi.org/10.1016/j.nicl.2013.09.011 |
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author | Anazodo, U.C. Shoemaker, J.K. Suskin, N. St. Lawrence, K.S. |
author_facet | Anazodo, U.C. Shoemaker, J.K. Suskin, N. St. Lawrence, K.S. |
author_sort | Anazodo, U.C. |
collection | PubMed |
description | Cognitive function decline secondary to cardiovascular disease has been reported. However, little is known about the impact of coronary artery disease (CAD) on the aging brain macrostructure or whether exercise training, in the context of cardiovascular rehabilitation, can affect brain structure following a coronary event. This study employed voxel-based morphometry of high resolution structural MRI images to investigate; 1) changes in regional gray matter volume (GMV) in CAD patients compared to age-matched controls, and 2) the effects of a six-month exercise-based cardiovascular rehabilitation program on CAD-related GMV decline. Compared to controls, significant decreases in regional GMV were found in the superior, medial and inferior frontal gyrus; superior and inferior parietal gyrus; middle and superior temporal gyrus and in the posterior cerebellum of CAD patients. Cardiovascular rehabilitation was associated with the recovery of regional GMV in the superior frontal gyrus, superior temporal gyrus and posterior cerebellum of the CAD patients as well as the increase in GMV in the supplementary motor area. Total and regional GMV correlated with fitness level, defined by the maximal oxygen consumption (VO(2)max), at baseline but not after cardiovascular rehabilitation. This study demonstrates that cardiovascular disease can adversely affect age-related decline in GMV; and that these disease-related effects could be mitigated by moderate levels of exercise training as part of cardiovascular rehabilitation. |
format | Online Article Text |
id | pubmed-3814972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-38149722013-11-22 An investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation() Anazodo, U.C. Shoemaker, J.K. Suskin, N. St. Lawrence, K.S. Neuroimage Clin Article Cognitive function decline secondary to cardiovascular disease has been reported. However, little is known about the impact of coronary artery disease (CAD) on the aging brain macrostructure or whether exercise training, in the context of cardiovascular rehabilitation, can affect brain structure following a coronary event. This study employed voxel-based morphometry of high resolution structural MRI images to investigate; 1) changes in regional gray matter volume (GMV) in CAD patients compared to age-matched controls, and 2) the effects of a six-month exercise-based cardiovascular rehabilitation program on CAD-related GMV decline. Compared to controls, significant decreases in regional GMV were found in the superior, medial and inferior frontal gyrus; superior and inferior parietal gyrus; middle and superior temporal gyrus and in the posterior cerebellum of CAD patients. Cardiovascular rehabilitation was associated with the recovery of regional GMV in the superior frontal gyrus, superior temporal gyrus and posterior cerebellum of the CAD patients as well as the increase in GMV in the supplementary motor area. Total and regional GMV correlated with fitness level, defined by the maximal oxygen consumption (VO(2)max), at baseline but not after cardiovascular rehabilitation. This study demonstrates that cardiovascular disease can adversely affect age-related decline in GMV; and that these disease-related effects could be mitigated by moderate levels of exercise training as part of cardiovascular rehabilitation. Elsevier 2013-10-06 /pmc/articles/PMC3814972/ /pubmed/24273722 http://dx.doi.org/10.1016/j.nicl.2013.09.011 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Anazodo, U.C. Shoemaker, J.K. Suskin, N. St. Lawrence, K.S. An investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation() |
title | An investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation() |
title_full | An investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation() |
title_fullStr | An investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation() |
title_full_unstemmed | An investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation() |
title_short | An investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation() |
title_sort | investigation of changes in regional gray matter volume in cardiovascular disease patients, pre and post cardiovascular rehabilitation() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814972/ https://www.ncbi.nlm.nih.gov/pubmed/24273722 http://dx.doi.org/10.1016/j.nicl.2013.09.011 |
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