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Small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability
PURPOSE OF REVIEW: Atherosclerotic plaque rupture and subsequent acute events, such as myocardial infarction and stroke, contribute to the majority of cardiovascular-related deaths. Calcification has emerged as a significant predictor of cardiovascular morbidity and mortality, challenging previously...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166045/ https://www.ncbi.nlm.nih.gov/pubmed/25188916 http://dx.doi.org/10.1097/MOL.0000000000000105 |
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author | Hutcheson, Joshua D. Maldonado, Natalia Aikawa, Elena |
author_facet | Hutcheson, Joshua D. Maldonado, Natalia Aikawa, Elena |
author_sort | Hutcheson, Joshua D. |
collection | PubMed |
description | PURPOSE OF REVIEW: Atherosclerotic plaque rupture and subsequent acute events, such as myocardial infarction and stroke, contribute to the majority of cardiovascular-related deaths. Calcification has emerged as a significant predictor of cardiovascular morbidity and mortality, challenging previously held notions that calcifications stabilize atherosclerotic plaques. In this review, we address this discrepancy through recent findings that not all calcifications are equivalent in determining plaque stability. RECENT FINDINGS: The risk associated with calcification is inversely associated with calcification density. As opposed to large calcifications that potentially stabilize the plaque, biomechanical modeling indicates that small microcalcifications within the plaque fibrous cap can lead to sufficient stress accumulation to cause plaque rupture. Microcalcifications appear to derive from matrix vesicles enriched in calcium-binding proteins that are released by cells within the plaque. Clinical detection of microcalcifications has been hampered by the lack of imaging resolution required for in-vivo visualization; however, recent studies have demonstrated promising new techniques to predict the presence of microcalcifications. SUMMARY: Microcalcifications play a major role in destabilizing atherosclerotic plaques. The identification of critical characteristics that lead to instability along with new imaging modalities to detect their presence in vivo may allow early identification and prevention of acute cardiovascular events. |
format | Online Article Text |
id | pubmed-4166045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-41660452014-09-22 Small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability Hutcheson, Joshua D. Maldonado, Natalia Aikawa, Elena Curr Opin Lipidol ATHEROSCLEROSIS: CELL BIOLOGY AND LIPOPROTEINS: Edited by Andrew Newby and Yury Miller PURPOSE OF REVIEW: Atherosclerotic plaque rupture and subsequent acute events, such as myocardial infarction and stroke, contribute to the majority of cardiovascular-related deaths. Calcification has emerged as a significant predictor of cardiovascular morbidity and mortality, challenging previously held notions that calcifications stabilize atherosclerotic plaques. In this review, we address this discrepancy through recent findings that not all calcifications are equivalent in determining plaque stability. RECENT FINDINGS: The risk associated with calcification is inversely associated with calcification density. As opposed to large calcifications that potentially stabilize the plaque, biomechanical modeling indicates that small microcalcifications within the plaque fibrous cap can lead to sufficient stress accumulation to cause plaque rupture. Microcalcifications appear to derive from matrix vesicles enriched in calcium-binding proteins that are released by cells within the plaque. Clinical detection of microcalcifications has been hampered by the lack of imaging resolution required for in-vivo visualization; however, recent studies have demonstrated promising new techniques to predict the presence of microcalcifications. SUMMARY: Microcalcifications play a major role in destabilizing atherosclerotic plaques. The identification of critical characteristics that lead to instability along with new imaging modalities to detect their presence in vivo may allow early identification and prevention of acute cardiovascular events. Lippincott Williams & Wilkins 2014-10 2014-09-04 /pmc/articles/PMC4166045/ /pubmed/25188916 http://dx.doi.org/10.1097/MOL.0000000000000105 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | ATHEROSCLEROSIS: CELL BIOLOGY AND LIPOPROTEINS: Edited by Andrew Newby and Yury Miller Hutcheson, Joshua D. Maldonado, Natalia Aikawa, Elena Small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability |
title | Small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability |
title_full | Small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability |
title_fullStr | Small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability |
title_full_unstemmed | Small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability |
title_short | Small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability |
title_sort | small entities with large impact: microcalcifications and atherosclerotic plaque vulnerability |
topic | ATHEROSCLEROSIS: CELL BIOLOGY AND LIPOPROTEINS: Edited by Andrew Newby and Yury Miller |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166045/ https://www.ncbi.nlm.nih.gov/pubmed/25188916 http://dx.doi.org/10.1097/MOL.0000000000000105 |
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