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Accelerating cine-MR Imaging in Mouse Hearts Using Compressed Sensing
PURPOSE: To combine global cardiac function imaging with compressed sensing (CS) in order to reduce scan time and to validate this technique in normal mouse hearts and in a murine model of chronic myocardial infarction. MATERIALS AND METHODS: To determine the maximally achievable acceleration factor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Subscription Services, Inc., A Wiley Company
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261377/ https://www.ncbi.nlm.nih.gov/pubmed/21932360 http://dx.doi.org/10.1002/jmri.22718 |
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author | Wech, Tobias Lemke, Angela Medway, Debra Stork, Lee-Anne Lygate, Craig A Neubauer, Stefan Köstler, Herbert Schneider, Jürgen E |
author_facet | Wech, Tobias Lemke, Angela Medway, Debra Stork, Lee-Anne Lygate, Craig A Neubauer, Stefan Köstler, Herbert Schneider, Jürgen E |
author_sort | Wech, Tobias |
collection | PubMed |
description | PURPOSE: To combine global cardiac function imaging with compressed sensing (CS) in order to reduce scan time and to validate this technique in normal mouse hearts and in a murine model of chronic myocardial infarction. MATERIALS AND METHODS: To determine the maximally achievable acceleration factor, fully acquired cine data, obtained in sham and chronically infarcted (MI) mouse hearts were 2–4-fold undersampled retrospectively, followed by CS reconstruction and blinded image segmentation. Subsequently, dedicated CS sampling schemes were implemented at a preclinical 9.4 T magnetic resonance imaging (MRI) system, and 2- and 3-fold undersampled cine data were acquired in normal mouse hearts with high temporal and spatial resolution. RESULTS: The retrospective analysis demonstrated that an undersampling factor of three is feasible without impairing accuracy of cardiac functional parameters. Dedicated CS sampling schemes applied prospectively to normal mouse hearts yielded comparable left-ventricular functional parameters, and intra- and interobserver variability between fully and 3-fold undersampled data. CONCLUSION: This study introduces and validates an alternative means to speed up experimental cine-MRI without the need for expensive hardware. J. Magn. Reson. Imaging 2011. © 2011 Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-3261377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Wiley Subscription Services, Inc., A Wiley Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-32613772012-01-20 Accelerating cine-MR Imaging in Mouse Hearts Using Compressed Sensing Wech, Tobias Lemke, Angela Medway, Debra Stork, Lee-Anne Lygate, Craig A Neubauer, Stefan Köstler, Herbert Schneider, Jürgen E J Magn Reson Imaging Original Research PURPOSE: To combine global cardiac function imaging with compressed sensing (CS) in order to reduce scan time and to validate this technique in normal mouse hearts and in a murine model of chronic myocardial infarction. MATERIALS AND METHODS: To determine the maximally achievable acceleration factor, fully acquired cine data, obtained in sham and chronically infarcted (MI) mouse hearts were 2–4-fold undersampled retrospectively, followed by CS reconstruction and blinded image segmentation. Subsequently, dedicated CS sampling schemes were implemented at a preclinical 9.4 T magnetic resonance imaging (MRI) system, and 2- and 3-fold undersampled cine data were acquired in normal mouse hearts with high temporal and spatial resolution. RESULTS: The retrospective analysis demonstrated that an undersampling factor of three is feasible without impairing accuracy of cardiac functional parameters. Dedicated CS sampling schemes applied prospectively to normal mouse hearts yielded comparable left-ventricular functional parameters, and intra- and interobserver variability between fully and 3-fold undersampled data. CONCLUSION: This study introduces and validates an alternative means to speed up experimental cine-MRI without the need for expensive hardware. J. Magn. Reson. Imaging 2011. © 2011 Wiley Periodicals, Inc. Wiley Subscription Services, Inc., A Wiley Company 2011-11 /pmc/articles/PMC3261377/ /pubmed/21932360 http://dx.doi.org/10.1002/jmri.22718 Text en Copyright © 2011 Wiley-Liss, Inc., A Wiley Company http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Research Wech, Tobias Lemke, Angela Medway, Debra Stork, Lee-Anne Lygate, Craig A Neubauer, Stefan Köstler, Herbert Schneider, Jürgen E Accelerating cine-MR Imaging in Mouse Hearts Using Compressed Sensing |
title | Accelerating cine-MR Imaging in Mouse Hearts Using Compressed Sensing |
title_full | Accelerating cine-MR Imaging in Mouse Hearts Using Compressed Sensing |
title_fullStr | Accelerating cine-MR Imaging in Mouse Hearts Using Compressed Sensing |
title_full_unstemmed | Accelerating cine-MR Imaging in Mouse Hearts Using Compressed Sensing |
title_short | Accelerating cine-MR Imaging in Mouse Hearts Using Compressed Sensing |
title_sort | accelerating cine-mr imaging in mouse hearts using compressed sensing |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261377/ https://www.ncbi.nlm.nih.gov/pubmed/21932360 http://dx.doi.org/10.1002/jmri.22718 |
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