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...
Autores principales: | , , , , , , , , |
---|---|
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 |