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Positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review
Atherosclerosis is the primary underlying cause of cardiovascular disease (CVD). It is the leading cause of morbidity and mortality in the Western world today and is set to become the prevailing disease and major cause of death worldwide by 2020. In the 1950s surgical intervention was introduced to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237171/ https://www.ncbi.nlm.nih.gov/pubmed/24289282 http://dx.doi.org/10.1111/cpf.12105 |
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author | Pedersen, Sune F Hag, Anne Mette F Klausen, Thomas L Ripa, Rasmus S Bodholdt, Rasmus P Kjær, Andreas |
author_facet | Pedersen, Sune F Hag, Anne Mette F Klausen, Thomas L Ripa, Rasmus S Bodholdt, Rasmus P Kjær, Andreas |
author_sort | Pedersen, Sune F |
collection | PubMed |
description | Atherosclerosis is the primary underlying cause of cardiovascular disease (CVD). It is the leading cause of morbidity and mortality in the Western world today and is set to become the prevailing disease and major cause of death worldwide by 2020. In the 1950s surgical intervention was introduced to treat symptomatic patients with high-grade carotid artery stenosis due to atherosclerosis – a procedure known as carotid endarterectomy (CEA). By removing the atherosclerotic plaque from the affected carotid artery of these patients, CEA is beneficial by preventing subsequent ipsilateral ischemic stroke. However, it is known that patients with low to intermediate artery stenosis may still experience ischemic events, leading clinicians to consider plaque composition as an important feature of atherosclerosis. Today molecular imaging can be used for characterization, visualization and quantification of cellular and subcellular physiological processes as they take place in vivo; using this technology we can obtain valuable information on atherosclerostic plaque composition. Applying molecular imaging clinically to atherosclerotic disease therefore has the potential to identify atherosclerotic plaques vulnerable to rupture. This could prove to be an important tool for the selection of patients for CEA surgery in a health system increasingly focused on individualized treatment. This review focuses on current advances and future developments of in vivo atherosclerosis PET imaging in man. |
format | Online Article Text |
id | pubmed-4237171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42371712014-12-15 Positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review Pedersen, Sune F Hag, Anne Mette F Klausen, Thomas L Ripa, Rasmus S Bodholdt, Rasmus P Kjær, Andreas Clin Physiol Funct Imaging Invited Reviews Atherosclerosis is the primary underlying cause of cardiovascular disease (CVD). It is the leading cause of morbidity and mortality in the Western world today and is set to become the prevailing disease and major cause of death worldwide by 2020. In the 1950s surgical intervention was introduced to treat symptomatic patients with high-grade carotid artery stenosis due to atherosclerosis – a procedure known as carotid endarterectomy (CEA). By removing the atherosclerotic plaque from the affected carotid artery of these patients, CEA is beneficial by preventing subsequent ipsilateral ischemic stroke. However, it is known that patients with low to intermediate artery stenosis may still experience ischemic events, leading clinicians to consider plaque composition as an important feature of atherosclerosis. Today molecular imaging can be used for characterization, visualization and quantification of cellular and subcellular physiological processes as they take place in vivo; using this technology we can obtain valuable information on atherosclerostic plaque composition. Applying molecular imaging clinically to atherosclerotic disease therefore has the potential to identify atherosclerotic plaques vulnerable to rupture. This could prove to be an important tool for the selection of patients for CEA surgery in a health system increasingly focused on individualized treatment. This review focuses on current advances and future developments of in vivo atherosclerosis PET imaging in man. BlackWell Publishing Ltd 2014-11 2013-12-01 /pmc/articles/PMC4237171/ /pubmed/24289282 http://dx.doi.org/10.1111/cpf.12105 Text en © 2013 The Authors. Clinical Physiology and Functional Imaging published by John Wiley & Sons Ltd on behalf of Scandinavian Society of Clinical Physiology and Nuclear Medicine. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 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 | Invited Reviews Pedersen, Sune F Hag, Anne Mette F Klausen, Thomas L Ripa, Rasmus S Bodholdt, Rasmus P Kjær, Andreas Positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review |
title | Positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review |
title_full | Positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review |
title_fullStr | Positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review |
title_full_unstemmed | Positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review |
title_short | Positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review |
title_sort | positron emission tomography of the vulnerable atherosclerotic plaque in man – a contemporary review |
topic | Invited Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237171/ https://www.ncbi.nlm.nih.gov/pubmed/24289282 http://dx.doi.org/10.1111/cpf.12105 |
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