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Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction

BACKGROUND: Mice are frequently used in research to examine outcomes of myocardial infarction (MI) and to investigate therapeutic interventions at an early pre-clinical stage. The MI model is generated by surgically occluding a major coronary artery, but natural variation in murine coronary anatomy...

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Autores principales: Redgrave, Rachael E., Tual-Chalot, Simon, Davison, Benjamin J., Greally, Elizabeth, Santibanez-Koref, Mauro, Schneider, Jurgen E., Blamire, Andrew M., Arthur, Helen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111480/
https://www.ncbi.nlm.nih.gov/pubmed/27882341
http://dx.doi.org/10.1016/j.ijcha.2016.03.005
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author Redgrave, Rachael E.
Tual-Chalot, Simon
Davison, Benjamin J.
Greally, Elizabeth
Santibanez-Koref, Mauro
Schneider, Jurgen E.
Blamire, Andrew M.
Arthur, Helen M.
author_facet Redgrave, Rachael E.
Tual-Chalot, Simon
Davison, Benjamin J.
Greally, Elizabeth
Santibanez-Koref, Mauro
Schneider, Jurgen E.
Blamire, Andrew M.
Arthur, Helen M.
author_sort Redgrave, Rachael E.
collection PubMed
description BACKGROUND: Mice are frequently used in research to examine outcomes of myocardial infarction (MI) and to investigate therapeutic interventions at an early pre-clinical stage. The MI model is generated by surgically occluding a major coronary artery, but natural variation in murine coronary anatomy can generate variable outcomes that will inevitably affect the accuracy of such investigations. The aim of this study was to use MRI to derive the most sensitive early variable that could be used to predict subsequent adverse cardiac remodelling in a male mouse model of MI. METHODS: Using a longitudinal study design, heart structure and function were evaluated using cardiac MRI at one week following surgical MI to generate the early measurements and again at four weeks, when the scar had matured. The primary variables measured at week one were left ventricular volumes at end systole (LV-ESV) and at end diastole (LV-EDV), infarct size, LV-cardiac mass, and ejection fraction (EF). RESULTS: Univariate and multiple regression analyses showed that LV-ESV at one week following MI could be used to accurately predict various parameters of adverse LV remodelling at four weeks post-MI. However, the highest correlation was between LV-ESV at one week following MI and LV-EDV at four weeks (r = 0.99; p < 0.0001), making LV-ESV at one week a valuable predictor variable of future adverse ventricular remodelling after MI. CONCLUSION: Using MRI to determine LV-ESV at an early stage following MI enables a more robust analysis of potential therapeutic interventions to ameliorate adverse cardiac remodelling.
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spelling pubmed-51114802016-11-21 Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction Redgrave, Rachael E. Tual-Chalot, Simon Davison, Benjamin J. Greally, Elizabeth Santibanez-Koref, Mauro Schneider, Jurgen E. Blamire, Andrew M. Arthur, Helen M. Int J Cardiol Heart Vasc Article BACKGROUND: Mice are frequently used in research to examine outcomes of myocardial infarction (MI) and to investigate therapeutic interventions at an early pre-clinical stage. The MI model is generated by surgically occluding a major coronary artery, but natural variation in murine coronary anatomy can generate variable outcomes that will inevitably affect the accuracy of such investigations. The aim of this study was to use MRI to derive the most sensitive early variable that could be used to predict subsequent adverse cardiac remodelling in a male mouse model of MI. METHODS: Using a longitudinal study design, heart structure and function were evaluated using cardiac MRI at one week following surgical MI to generate the early measurements and again at four weeks, when the scar had matured. The primary variables measured at week one were left ventricular volumes at end systole (LV-ESV) and at end diastole (LV-EDV), infarct size, LV-cardiac mass, and ejection fraction (EF). RESULTS: Univariate and multiple regression analyses showed that LV-ESV at one week following MI could be used to accurately predict various parameters of adverse LV remodelling at four weeks post-MI. However, the highest correlation was between LV-ESV at one week following MI and LV-EDV at four weeks (r = 0.99; p < 0.0001), making LV-ESV at one week a valuable predictor variable of future adverse ventricular remodelling after MI. CONCLUSION: Using MRI to determine LV-ESV at an early stage following MI enables a more robust analysis of potential therapeutic interventions to ameliorate adverse cardiac remodelling. Elsevier 2016-03-16 /pmc/articles/PMC5111480/ /pubmed/27882341 http://dx.doi.org/10.1016/j.ijcha.2016.03.005 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Redgrave, Rachael E.
Tual-Chalot, Simon
Davison, Benjamin J.
Greally, Elizabeth
Santibanez-Koref, Mauro
Schneider, Jurgen E.
Blamire, Andrew M.
Arthur, Helen M.
Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction
title Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction
title_full Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction
title_fullStr Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction
title_full_unstemmed Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction
title_short Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction
title_sort using mri to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111480/
https://www.ncbi.nlm.nih.gov/pubmed/27882341
http://dx.doi.org/10.1016/j.ijcha.2016.03.005
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