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Detecting native and bioprosthetic aortic valve disease using (18)F-sodium fluoride: Clinical implications
Calcific aortic valve disease is the most common valvular disease and confers significant morbidity and mortality. There are currently no medical therapies that successfully halt or reverse the disease progression, making surgical replacement the only treatment currently available. The majority of p...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076133/ https://www.ncbi.nlm.nih.gov/pubmed/33175301 http://dx.doi.org/10.1007/s12350-020-02411-x |
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author | Fletcher, Alexander J. Dweck, Marc R. |
author_facet | Fletcher, Alexander J. Dweck, Marc R. |
author_sort | Fletcher, Alexander J. |
collection | PubMed |
description | Calcific aortic valve disease is the most common valvular disease and confers significant morbidity and mortality. There are currently no medical therapies that successfully halt or reverse the disease progression, making surgical replacement the only treatment currently available. The majority of patients will receive a bioprosthetic valve, which themselves are prone to degeneration and may also need replaced, adding to the already substantial healthcare burden of aortic stenosis. Echocardiography and computed tomography can identify late-stage manifestations of the disease process affecting native and bioprosthetic aortic valves but cannot detect or quantify early molecular changes. (18)F-fluoride positron emission tomography, on the other hand, can non-invasively and sensitively assess disease activity in the valves. The current review outlines the pivotal role this novel molecular imaging technique has played in improving our understanding of native and bioprosthetic aortic valve disease, as well as providing insights into its feasibility as an important future research and clinical tool. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12350-020-02411-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-8076133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-80761332021-05-05 Detecting native and bioprosthetic aortic valve disease using (18)F-sodium fluoride: Clinical implications Fletcher, Alexander J. Dweck, Marc R. J Nucl Cardiol Molecular Imaging Corner Calcific aortic valve disease is the most common valvular disease and confers significant morbidity and mortality. There are currently no medical therapies that successfully halt or reverse the disease progression, making surgical replacement the only treatment currently available. The majority of patients will receive a bioprosthetic valve, which themselves are prone to degeneration and may also need replaced, adding to the already substantial healthcare burden of aortic stenosis. Echocardiography and computed tomography can identify late-stage manifestations of the disease process affecting native and bioprosthetic aortic valves but cannot detect or quantify early molecular changes. (18)F-fluoride positron emission tomography, on the other hand, can non-invasively and sensitively assess disease activity in the valves. The current review outlines the pivotal role this novel molecular imaging technique has played in improving our understanding of native and bioprosthetic aortic valve disease, as well as providing insights into its feasibility as an important future research and clinical tool. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12350-020-02411-x) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-11-11 2021 /pmc/articles/PMC8076133/ /pubmed/33175301 http://dx.doi.org/10.1007/s12350-020-02411-x Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Molecular Imaging Corner Fletcher, Alexander J. Dweck, Marc R. Detecting native and bioprosthetic aortic valve disease using (18)F-sodium fluoride: Clinical implications |
title | Detecting native and bioprosthetic aortic valve disease using (18)F-sodium fluoride: Clinical implications |
title_full | Detecting native and bioprosthetic aortic valve disease using (18)F-sodium fluoride: Clinical implications |
title_fullStr | Detecting native and bioprosthetic aortic valve disease using (18)F-sodium fluoride: Clinical implications |
title_full_unstemmed | Detecting native and bioprosthetic aortic valve disease using (18)F-sodium fluoride: Clinical implications |
title_short | Detecting native and bioprosthetic aortic valve disease using (18)F-sodium fluoride: Clinical implications |
title_sort | detecting native and bioprosthetic aortic valve disease using (18)f-sodium fluoride: clinical implications |
topic | Molecular Imaging Corner |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076133/ https://www.ncbi.nlm.nih.gov/pubmed/33175301 http://dx.doi.org/10.1007/s12350-020-02411-x |
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