Cargando…

Temporal and spatial characteristics of the area at risk investigated using computed tomography and T(1)-weighted magnetic resonance imaging

AIMS: Cardiovascular magnetic resonance (CMR) imaging can measure the myocardial area at risk (AAR), but the technique has received criticism for inadequate validation. CMR commonly depicts an AAR that is wider than the infarct, which in turn would require a lateral perfusion gradient within the AAR...

Descripción completa

Detalles Bibliográficos
Autores principales: van der Pals, Jesper, Hammer-Hansen, Sophia, Nielles-Vallespin, Sonia, Kellman, Peter, Taylor, Joni, Kozlov, Shawn, Hsu, Li-Yueh, Chen, Marcus Y., Arai, Andrew E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609161/
https://www.ncbi.nlm.nih.gov/pubmed/25881901
http://dx.doi.org/10.1093/ehjci/jev072
_version_ 1782395781007802368
author van der Pals, Jesper
Hammer-Hansen, Sophia
Nielles-Vallespin, Sonia
Kellman, Peter
Taylor, Joni
Kozlov, Shawn
Hsu, Li-Yueh
Chen, Marcus Y.
Arai, Andrew E.
author_facet van der Pals, Jesper
Hammer-Hansen, Sophia
Nielles-Vallespin, Sonia
Kellman, Peter
Taylor, Joni
Kozlov, Shawn
Hsu, Li-Yueh
Chen, Marcus Y.
Arai, Andrew E.
author_sort van der Pals, Jesper
collection PubMed
description AIMS: Cardiovascular magnetic resonance (CMR) imaging can measure the myocardial area at risk (AAR), but the technique has received criticism for inadequate validation. CMR commonly depicts an AAR that is wider than the infarct, which in turn would require a lateral perfusion gradient within the AAR. We investigated the presence of a lateral perfusion gradient within the AAR and validated CMR measures of AAR against three independent reference standards of high quality. METHODS AND RESULTS: Computed tomography (CT) perfusion imaging, microsphere blood flow analysis, T(1)-weighted 3T CMR and fluorescent microparticle pathology were used to investigate the AAR in a canine model (n = 10) of ischaemia and reperfusion. AAR size by CMR correlated well with CT (R(2) = 0.80), microsphere blood flow (R(2) = 0.80), and pathology (R(2) = 0.74) with good limits of agreement [−0.79 ± 4.02% of the left ventricular mass (LVM) vs. CT; −1.49 ± 4.04% LVM vs. blood flow and −1.01 ± 4.18% LVM vs. pathology]. The lateral portion of the AAR had higher perfusion than the core of the AAR by CT perfusion imaging (40.7 ± 11.8 vs. 25.2 ± 17.7 Hounsfield units, P = 0.0008) and microsphere blood flow (0.11 ± 0.04 vs. 0.05 ± 0.02 mL/g/min, lateral vs. core, P = 0.001). The transmural extent of MI was lower in the lateral portion of the AAR than the core (28.2 ± 10.2 vs. 17.4 ± 8.4% of the wall, P = 0.001). CONCLUSION: T(1)-weighted CMR accurately quantifies size of the AAR with excellent agreement compared with three independent reference standards. A lateral perfusion gradient results in lower transmural extent of infarction at the edges of the AAR compared with the core.
format Online
Article
Text
id pubmed-4609161
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-46091612015-10-19 Temporal and spatial characteristics of the area at risk investigated using computed tomography and T(1)-weighted magnetic resonance imaging van der Pals, Jesper Hammer-Hansen, Sophia Nielles-Vallespin, Sonia Kellman, Peter Taylor, Joni Kozlov, Shawn Hsu, Li-Yueh Chen, Marcus Y. Arai, Andrew E. Eur Heart J Cardiovasc Imaging Original Articles AIMS: Cardiovascular magnetic resonance (CMR) imaging can measure the myocardial area at risk (AAR), but the technique has received criticism for inadequate validation. CMR commonly depicts an AAR that is wider than the infarct, which in turn would require a lateral perfusion gradient within the AAR. We investigated the presence of a lateral perfusion gradient within the AAR and validated CMR measures of AAR against three independent reference standards of high quality. METHODS AND RESULTS: Computed tomography (CT) perfusion imaging, microsphere blood flow analysis, T(1)-weighted 3T CMR and fluorescent microparticle pathology were used to investigate the AAR in a canine model (n = 10) of ischaemia and reperfusion. AAR size by CMR correlated well with CT (R(2) = 0.80), microsphere blood flow (R(2) = 0.80), and pathology (R(2) = 0.74) with good limits of agreement [−0.79 ± 4.02% of the left ventricular mass (LVM) vs. CT; −1.49 ± 4.04% LVM vs. blood flow and −1.01 ± 4.18% LVM vs. pathology]. The lateral portion of the AAR had higher perfusion than the core of the AAR by CT perfusion imaging (40.7 ± 11.8 vs. 25.2 ± 17.7 Hounsfield units, P = 0.0008) and microsphere blood flow (0.11 ± 0.04 vs. 0.05 ± 0.02 mL/g/min, lateral vs. core, P = 0.001). The transmural extent of MI was lower in the lateral portion of the AAR than the core (28.2 ± 10.2 vs. 17.4 ± 8.4% of the wall, P = 0.001). CONCLUSION: T(1)-weighted CMR accurately quantifies size of the AAR with excellent agreement compared with three independent reference standards. A lateral perfusion gradient results in lower transmural extent of infarction at the edges of the AAR compared with the core. Oxford University Press 2015-11 2015-04-16 /pmc/articles/PMC4609161/ /pubmed/25881901 http://dx.doi.org/10.1093/ehjci/jev072 Text en © The Author 2015. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
van der Pals, Jesper
Hammer-Hansen, Sophia
Nielles-Vallespin, Sonia
Kellman, Peter
Taylor, Joni
Kozlov, Shawn
Hsu, Li-Yueh
Chen, Marcus Y.
Arai, Andrew E.
Temporal and spatial characteristics of the area at risk investigated using computed tomography and T(1)-weighted magnetic resonance imaging
title Temporal and spatial characteristics of the area at risk investigated using computed tomography and T(1)-weighted magnetic resonance imaging
title_full Temporal and spatial characteristics of the area at risk investigated using computed tomography and T(1)-weighted magnetic resonance imaging
title_fullStr Temporal and spatial characteristics of the area at risk investigated using computed tomography and T(1)-weighted magnetic resonance imaging
title_full_unstemmed Temporal and spatial characteristics of the area at risk investigated using computed tomography and T(1)-weighted magnetic resonance imaging
title_short Temporal and spatial characteristics of the area at risk investigated using computed tomography and T(1)-weighted magnetic resonance imaging
title_sort temporal and spatial characteristics of the area at risk investigated using computed tomography and t(1)-weighted magnetic resonance imaging
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609161/
https://www.ncbi.nlm.nih.gov/pubmed/25881901
http://dx.doi.org/10.1093/ehjci/jev072
work_keys_str_mv AT vanderpalsjesper temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging
AT hammerhansensophia temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging
AT niellesvallespinsonia temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging
AT kellmanpeter temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging
AT taylorjoni temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging
AT kozlovshawn temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging
AT hsuliyueh temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging
AT chenmarcusy temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging
AT araiandrewe temporalandspatialcharacteristicsoftheareaatriskinvestigatedusingcomputedtomographyandt1weightedmagneticresonanceimaging