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Feasibility of simultaneous PET-MR perfusion using a novel cardiac perfusion phantom
BACKGROUND: PET-MR scanners are beginning to be employed for quantitative myocardial perfusion imaging. In order to examine simultaneous perfusion calculations, this work describes a feasibility study of simultaneous PET-MR of gadolinium-based contrast agent (GBCA) and PET radiotracer in a novel car...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954708/ https://www.ncbi.nlm.nih.gov/pubmed/29782598 http://dx.doi.org/10.1186/s41824-017-0008-9 |
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author | O’Doherty, Jim Sammut, Eva Schleyer, Paul Stirling, James Nazir, Muhummad Sohaib Marsden, Paul K. Chiribiri, Amedeo |
author_facet | O’Doherty, Jim Sammut, Eva Schleyer, Paul Stirling, James Nazir, Muhummad Sohaib Marsden, Paul K. Chiribiri, Amedeo |
author_sort | O’Doherty, Jim |
collection | PubMed |
description | BACKGROUND: PET-MR scanners are beginning to be employed for quantitative myocardial perfusion imaging. In order to examine simultaneous perfusion calculations, this work describes a feasibility study of simultaneous PET-MR of gadolinium-based contrast agent (GBCA) and PET radiotracer in a novel cardiac perfusion phantom. RESULTS: [(18)F]F(−) and GBCA were injected simultaneously into a cardiac phantom using a range of ground-truth myocardial perfusion rates of 1 to 5 ml/g/min. PET quantification of K (1) (ml/g/min) was performed using a single tissue compartment model. MR perfusion was calculated using a model-independent signal deconvolution technique. PET and MR signal traces from the phantom aorta and myocardial sections show true simultaneous PET and MR arterial input functions (AIF) and myocardial uptake respectively at each perfusion rate. Calculation of perfusion parameters showed both K (1) and h(t = 0) (PET and MR perfusion parameters respectively) to be linearly related with the ground truth perfusion rate (P (T)), and also linearly related to each other (R(2) = 0.99). The highest difference in perfusion values between K (1) and P (T) was 16% at 1 ml/g/min, and the mean difference for all other perfusion rates was <3%. CONCLUSIONS: The perfusion phantom allows accurate and reproducible simulation of the myocardial kinetics for simultaneous PET-MR imaging, and may find use in protocol design and development of PET-MR based quantification techniques and direct comparison of quantification of the two modalities. |
format | Online Article Text |
id | pubmed-5954708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-59547082018-05-18 Feasibility of simultaneous PET-MR perfusion using a novel cardiac perfusion phantom O’Doherty, Jim Sammut, Eva Schleyer, Paul Stirling, James Nazir, Muhummad Sohaib Marsden, Paul K. Chiribiri, Amedeo Eur J Hybrid Imaging Original Article BACKGROUND: PET-MR scanners are beginning to be employed for quantitative myocardial perfusion imaging. In order to examine simultaneous perfusion calculations, this work describes a feasibility study of simultaneous PET-MR of gadolinium-based contrast agent (GBCA) and PET radiotracer in a novel cardiac perfusion phantom. RESULTS: [(18)F]F(−) and GBCA were injected simultaneously into a cardiac phantom using a range of ground-truth myocardial perfusion rates of 1 to 5 ml/g/min. PET quantification of K (1) (ml/g/min) was performed using a single tissue compartment model. MR perfusion was calculated using a model-independent signal deconvolution technique. PET and MR signal traces from the phantom aorta and myocardial sections show true simultaneous PET and MR arterial input functions (AIF) and myocardial uptake respectively at each perfusion rate. Calculation of perfusion parameters showed both K (1) and h(t = 0) (PET and MR perfusion parameters respectively) to be linearly related with the ground truth perfusion rate (P (T)), and also linearly related to each other (R(2) = 0.99). The highest difference in perfusion values between K (1) and P (T) was 16% at 1 ml/g/min, and the mean difference for all other perfusion rates was <3%. CONCLUSIONS: The perfusion phantom allows accurate and reproducible simulation of the myocardial kinetics for simultaneous PET-MR imaging, and may find use in protocol design and development of PET-MR based quantification techniques and direct comparison of quantification of the two modalities. Springer International Publishing 2017-10-12 2017 /pmc/articles/PMC5954708/ /pubmed/29782598 http://dx.doi.org/10.1186/s41824-017-0008-9 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article O’Doherty, Jim Sammut, Eva Schleyer, Paul Stirling, James Nazir, Muhummad Sohaib Marsden, Paul K. Chiribiri, Amedeo Feasibility of simultaneous PET-MR perfusion using a novel cardiac perfusion phantom |
title | Feasibility of simultaneous PET-MR perfusion using a novel cardiac perfusion phantom |
title_full | Feasibility of simultaneous PET-MR perfusion using a novel cardiac perfusion phantom |
title_fullStr | Feasibility of simultaneous PET-MR perfusion using a novel cardiac perfusion phantom |
title_full_unstemmed | Feasibility of simultaneous PET-MR perfusion using a novel cardiac perfusion phantom |
title_short | Feasibility of simultaneous PET-MR perfusion using a novel cardiac perfusion phantom |
title_sort | feasibility of simultaneous pet-mr perfusion using a novel cardiac perfusion phantom |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954708/ https://www.ncbi.nlm.nih.gov/pubmed/29782598 http://dx.doi.org/10.1186/s41824-017-0008-9 |
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