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Rubidium-82 PET imaging is feasible in a rat myocardial infarction model

BACKGROUND: Small-animal myocardial infarct models are frequently used in the assessment of new cardioprotective strategies. A validated quantification of perfusion using a non-cyclotron-dependent PET tracer would be of importance in monitoring response to therapy. We tested whether myocardial PET p...

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Autores principales: Ghotbi, Adam Ali, Clemmensen, Andreas, Kyhl, Kasper, Follin, Bjarke, Hasbak, Philip, Engstrøm, Thomas, Ripa, Rasmus Sejersten, Kjaer, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517336/
https://www.ncbi.nlm.nih.gov/pubmed/28721647
http://dx.doi.org/10.1007/s12350-017-0994-9
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author Ghotbi, Adam Ali
Clemmensen, Andreas
Kyhl, Kasper
Follin, Bjarke
Hasbak, Philip
Engstrøm, Thomas
Ripa, Rasmus Sejersten
Kjaer, Andreas
author_facet Ghotbi, Adam Ali
Clemmensen, Andreas
Kyhl, Kasper
Follin, Bjarke
Hasbak, Philip
Engstrøm, Thomas
Ripa, Rasmus Sejersten
Kjaer, Andreas
author_sort Ghotbi, Adam Ali
collection PubMed
description BACKGROUND: Small-animal myocardial infarct models are frequently used in the assessment of new cardioprotective strategies. A validated quantification of perfusion using a non-cyclotron-dependent PET tracer would be of importance in monitoring response to therapy. We tested whether myocardial PET perfusion imaging is feasible with Rubidium-82 ((82)Rb) in a small-animal scanner using a rat myocardial infarct model. METHODS: 18 Sprague-Dawley rats underwent permanent coronary artery ligation (infarct group), and 11 rats underwent ischemia-reperfusion (reperfusion group) procedure. (82)Rb-PET and magnetic resonance imaging (MRI) were conducted before and after the intervention. Perfusion was compared to both left ventricle ejection fraction (LVEF) and infarct size assessed by MRI. RESULTS: Follow-up global (82)Rb-uptake correlated significantly with infarct size (infarct group: r = −0.81, P < 0.001 and reperfusion group: r = −0.61, P = 0.04). Only (82)Rb-uptake in the infarct group correlated with LVEF. At follow-up, a higher segmental (82)Rb-uptake in the infarct group was associated with better wall motion (β = 0.034, CI [0.028;0.039], P < 0.001, R(2) = 0.30), and inversely associated with scar transmurality (β = −2.4 [−2.6; −2.2], P < 0.001, R(2) = 0.59). The associations were similar for the reperfusion group. CONCLUSION: (82)Rb-PET is feasible in small animal scanners despite the long positron range and enables fast and time-efficient myocardial perfusion imaging in rat models. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12350-017-0994-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-65173362019-05-28 Rubidium-82 PET imaging is feasible in a rat myocardial infarction model Ghotbi, Adam Ali Clemmensen, Andreas Kyhl, Kasper Follin, Bjarke Hasbak, Philip Engstrøm, Thomas Ripa, Rasmus Sejersten Kjaer, Andreas J Nucl Cardiol Original Article BACKGROUND: Small-animal myocardial infarct models are frequently used in the assessment of new cardioprotective strategies. A validated quantification of perfusion using a non-cyclotron-dependent PET tracer would be of importance in monitoring response to therapy. We tested whether myocardial PET perfusion imaging is feasible with Rubidium-82 ((82)Rb) in a small-animal scanner using a rat myocardial infarct model. METHODS: 18 Sprague-Dawley rats underwent permanent coronary artery ligation (infarct group), and 11 rats underwent ischemia-reperfusion (reperfusion group) procedure. (82)Rb-PET and magnetic resonance imaging (MRI) were conducted before and after the intervention. Perfusion was compared to both left ventricle ejection fraction (LVEF) and infarct size assessed by MRI. RESULTS: Follow-up global (82)Rb-uptake correlated significantly with infarct size (infarct group: r = −0.81, P < 0.001 and reperfusion group: r = −0.61, P = 0.04). Only (82)Rb-uptake in the infarct group correlated with LVEF. At follow-up, a higher segmental (82)Rb-uptake in the infarct group was associated with better wall motion (β = 0.034, CI [0.028;0.039], P < 0.001, R(2) = 0.30), and inversely associated with scar transmurality (β = −2.4 [−2.6; −2.2], P < 0.001, R(2) = 0.59). The associations were similar for the reperfusion group. CONCLUSION: (82)Rb-PET is feasible in small animal scanners despite the long positron range and enables fast and time-efficient myocardial perfusion imaging in rat models. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12350-017-0994-9) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-07-18 2019 /pmc/articles/PMC6517336/ /pubmed/28721647 http://dx.doi.org/10.1007/s12350-017-0994-9 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
Ghotbi, Adam Ali
Clemmensen, Andreas
Kyhl, Kasper
Follin, Bjarke
Hasbak, Philip
Engstrøm, Thomas
Ripa, Rasmus Sejersten
Kjaer, Andreas
Rubidium-82 PET imaging is feasible in a rat myocardial infarction model
title Rubidium-82 PET imaging is feasible in a rat myocardial infarction model
title_full Rubidium-82 PET imaging is feasible in a rat myocardial infarction model
title_fullStr Rubidium-82 PET imaging is feasible in a rat myocardial infarction model
title_full_unstemmed Rubidium-82 PET imaging is feasible in a rat myocardial infarction model
title_short Rubidium-82 PET imaging is feasible in a rat myocardial infarction model
title_sort rubidium-82 pet imaging is feasible in a rat myocardial infarction model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517336/
https://www.ncbi.nlm.nih.gov/pubmed/28721647
http://dx.doi.org/10.1007/s12350-017-0994-9
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