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Variations in atherosclerosis and remodeling patterns in aorta and carotids
BACKGROUND: Atherosclerosis is a progressive disease that causes vascular remodeling that can be positive or negative. The evolution of arterial wall thickening and changes in lumen size under current "standard of care" in different arterial beds is unclear. The purpose of this study was t...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848016/ https://www.ncbi.nlm.nih.gov/pubmed/20205722 http://dx.doi.org/10.1186/1532-429X-12-10 |
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author | Hayashi, Katsumi Mani, Venkatesh Nemade, Ajay Aguiar, Silvia Postley, John E Fuster, Valentin Fayad, Zahi A |
author_facet | Hayashi, Katsumi Mani, Venkatesh Nemade, Ajay Aguiar, Silvia Postley, John E Fuster, Valentin Fayad, Zahi A |
author_sort | Hayashi, Katsumi |
collection | PubMed |
description | BACKGROUND: Atherosclerosis is a progressive disease that causes vascular remodeling that can be positive or negative. The evolution of arterial wall thickening and changes in lumen size under current "standard of care" in different arterial beds is unclear. The purpose of this study was to examine arterial remodeling and progression/regression of atherosclerosis in aorta and carotid arteries of individuals at risk for atherosclerosis normalized over a 1-year period. METHODS: In this study, 28 patients underwent at least 2 black-blood in vivo cardiovascular magnetic resonance (CMR) scans of aorta and carotids over a one-year period (Mean 17.8 ± 7.5 months). Clinical risk profiles for atherosclerosis and medications were documented and patients were followed by their referring physicians under current "standard of care" guidelines. Carotid and aortic wall lumen areas were matched across the time-points from cross-sectional images. RESULTS: The wall area increased by 8.67%, 10.64%, and 13.24% per year (carotid artery, thoracic aorta and abdominal aorta respectively, p < 0.001). The lumen area of the abdominal aorta increased by 4.97% per year (p = 0.002), but the carotid artery and thoracic aorta lumen areas did not change significantly. The use of statin therapy did not change the rate of increase of wall area of carotid artery, thoracic and abdominal aorta, but decreased the rate of change of lumen area of carotid artery (-3.08 ± 11.34 vs. 0.19 ± 12.91 p < 0.05). CONCLUSIONS: Results of this study of multiple vascular beds indicated that different vascular locations exhibited varying progression of atherosclerosis and remodeling as monitored by CMR. |
format | Text |
id | pubmed-2848016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28480162010-04-01 Variations in atherosclerosis and remodeling patterns in aorta and carotids Hayashi, Katsumi Mani, Venkatesh Nemade, Ajay Aguiar, Silvia Postley, John E Fuster, Valentin Fayad, Zahi A J Cardiovasc Magn Reson Research BACKGROUND: Atherosclerosis is a progressive disease that causes vascular remodeling that can be positive or negative. The evolution of arterial wall thickening and changes in lumen size under current "standard of care" in different arterial beds is unclear. The purpose of this study was to examine arterial remodeling and progression/regression of atherosclerosis in aorta and carotid arteries of individuals at risk for atherosclerosis normalized over a 1-year period. METHODS: In this study, 28 patients underwent at least 2 black-blood in vivo cardiovascular magnetic resonance (CMR) scans of aorta and carotids over a one-year period (Mean 17.8 ± 7.5 months). Clinical risk profiles for atherosclerosis and medications were documented and patients were followed by their referring physicians under current "standard of care" guidelines. Carotid and aortic wall lumen areas were matched across the time-points from cross-sectional images. RESULTS: The wall area increased by 8.67%, 10.64%, and 13.24% per year (carotid artery, thoracic aorta and abdominal aorta respectively, p < 0.001). The lumen area of the abdominal aorta increased by 4.97% per year (p = 0.002), but the carotid artery and thoracic aorta lumen areas did not change significantly. The use of statin therapy did not change the rate of increase of wall area of carotid artery, thoracic and abdominal aorta, but decreased the rate of change of lumen area of carotid artery (-3.08 ± 11.34 vs. 0.19 ± 12.91 p < 0.05). CONCLUSIONS: Results of this study of multiple vascular beds indicated that different vascular locations exhibited varying progression of atherosclerosis and remodeling as monitored by CMR. BioMed Central 2010-03-05 /pmc/articles/PMC2848016/ /pubmed/20205722 http://dx.doi.org/10.1186/1532-429X-12-10 Text en Copyright ©2010 Hayashi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Hayashi, Katsumi Mani, Venkatesh Nemade, Ajay Aguiar, Silvia Postley, John E Fuster, Valentin Fayad, Zahi A Variations in atherosclerosis and remodeling patterns in aorta and carotids |
title | Variations in atherosclerosis and remodeling patterns in aorta and carotids |
title_full | Variations in atherosclerosis and remodeling patterns in aorta and carotids |
title_fullStr | Variations in atherosclerosis and remodeling patterns in aorta and carotids |
title_full_unstemmed | Variations in atherosclerosis and remodeling patterns in aorta and carotids |
title_short | Variations in atherosclerosis and remodeling patterns in aorta and carotids |
title_sort | variations in atherosclerosis and remodeling patterns in aorta and carotids |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848016/ https://www.ncbi.nlm.nih.gov/pubmed/20205722 http://dx.doi.org/10.1186/1532-429X-12-10 |
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