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Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography
Vascular calcification is a complex biological process that is a hallmark of atherosclerosis. While macrocalcification confers plaque stability, microcalcification is a key feature of high-risk atheroma and is associated with increased morbidity and mortality. Positron emission tomography and X-ray...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506997/ https://www.ncbi.nlm.nih.gov/pubmed/26151378 http://dx.doi.org/10.1038/ncomms8495 |
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author | Irkle, Agnese Vesey, Alex T. Lewis, David Y. Skepper, Jeremy N. Bird, Joseph L. E. Dweck, Marc R. Joshi, Francis R. Gallagher, Ferdia A. Warburton, Elizabeth A. Bennett, Martin R. Brindle, Kevin M. Newby, David E. Rudd, James H. Davenport, Anthony P. |
author_facet | Irkle, Agnese Vesey, Alex T. Lewis, David Y. Skepper, Jeremy N. Bird, Joseph L. E. Dweck, Marc R. Joshi, Francis R. Gallagher, Ferdia A. Warburton, Elizabeth A. Bennett, Martin R. Brindle, Kevin M. Newby, David E. Rudd, James H. Davenport, Anthony P. |
author_sort | Irkle, Agnese |
collection | PubMed |
description | Vascular calcification is a complex biological process that is a hallmark of atherosclerosis. While macrocalcification confers plaque stability, microcalcification is a key feature of high-risk atheroma and is associated with increased morbidity and mortality. Positron emission tomography and X-ray computed tomography (PET/CT) imaging of atherosclerosis using (18)F-sodium fluoride ((18)F-NaF) has the potential to identify pathologically high-risk nascent microcalcification. However, the precise molecular mechanism of (18)F-NaF vascular uptake is still unknown. Here we use electron microscopy, autoradiography, histology and preclinical and clinical PET/CT to analyse (18)F-NaF binding. We show that (18)F-NaF adsorbs to calcified deposits within plaque with high affinity and is selective and specific. (18)F-NaF PET/CT imaging can distinguish between areas of macro- and microcalcification. This is the only currently available clinical imaging platform that can non-invasively detect microcalcification in active unstable atherosclerosis. The use of (18)F-NaF may foster new approaches to developing treatments for vascular calcification. |
format | Online Article Text |
id | pubmed-4506997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45069972015-07-21 Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography Irkle, Agnese Vesey, Alex T. Lewis, David Y. Skepper, Jeremy N. Bird, Joseph L. E. Dweck, Marc R. Joshi, Francis R. Gallagher, Ferdia A. Warburton, Elizabeth A. Bennett, Martin R. Brindle, Kevin M. Newby, David E. Rudd, James H. Davenport, Anthony P. Nat Commun Article Vascular calcification is a complex biological process that is a hallmark of atherosclerosis. While macrocalcification confers plaque stability, microcalcification is a key feature of high-risk atheroma and is associated with increased morbidity and mortality. Positron emission tomography and X-ray computed tomography (PET/CT) imaging of atherosclerosis using (18)F-sodium fluoride ((18)F-NaF) has the potential to identify pathologically high-risk nascent microcalcification. However, the precise molecular mechanism of (18)F-NaF vascular uptake is still unknown. Here we use electron microscopy, autoradiography, histology and preclinical and clinical PET/CT to analyse (18)F-NaF binding. We show that (18)F-NaF adsorbs to calcified deposits within plaque with high affinity and is selective and specific. (18)F-NaF PET/CT imaging can distinguish between areas of macro- and microcalcification. This is the only currently available clinical imaging platform that can non-invasively detect microcalcification in active unstable atherosclerosis. The use of (18)F-NaF may foster new approaches to developing treatments for vascular calcification. Nature Pub. Group 2015-07-07 /pmc/articles/PMC4506997/ /pubmed/26151378 http://dx.doi.org/10.1038/ncomms8495 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Irkle, Agnese Vesey, Alex T. Lewis, David Y. Skepper, Jeremy N. Bird, Joseph L. E. Dweck, Marc R. Joshi, Francis R. Gallagher, Ferdia A. Warburton, Elizabeth A. Bennett, Martin R. Brindle, Kevin M. Newby, David E. Rudd, James H. Davenport, Anthony P. Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography |
title | Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography |
title_full | Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography |
title_fullStr | Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography |
title_full_unstemmed | Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography |
title_short | Identifying active vascular microcalcification by (18)F-sodium fluoride positron emission tomography |
title_sort | identifying active vascular microcalcification by (18)f-sodium fluoride positron emission tomography |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506997/ https://www.ncbi.nlm.nih.gov/pubmed/26151378 http://dx.doi.org/10.1038/ncomms8495 |
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