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Longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study
BACKGROUND: Regional myocardial function is typically evaluated by visual assessment by experienced users, or by methods requiring substantial post processing time. Visual assessment is subjective and not quantitative. Therefore, the purpose of this study is to develop and validate a simple method t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3562217/ https://www.ncbi.nlm.nih.gov/pubmed/23343426 http://dx.doi.org/10.1186/1532-429X-15-15 |
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author | Heiberg, Einar Pahlm-Webb, Ulrika Agarwal, Shruti Bergvall, Erik Fransson, Helen Steding-Ehrenborg, Katarina Carlsson, Marcus Arheden, Håkan |
author_facet | Heiberg, Einar Pahlm-Webb, Ulrika Agarwal, Shruti Bergvall, Erik Fransson, Helen Steding-Ehrenborg, Katarina Carlsson, Marcus Arheden, Håkan |
author_sort | Heiberg, Einar |
collection | PubMed |
description | BACKGROUND: Regional myocardial function is typically evaluated by visual assessment by experienced users, or by methods requiring substantial post processing time. Visual assessment is subjective and not quantitative. Therefore, the purpose of this study is to develop and validate a simple method to derive quantitative measures of regional wall function from velocity encoded Cardiovascular Magnetic Resonance (CMR), and provide associated normal values for longitudinal strain. METHOD: Both fast field echo (FFE) and turbo field echo (TFE) velocity encoded CMR images were acquired in three long axis planes in 36 healthy volunteers (13 women, 23 men), age 35±12 years. Strain was also quantified in 10 patients within one week after myocardial infarction. The user manually delineated myocardium in one time frame and strain was calculated as the myocardium was tracked throughout the cardiac cycle using an optimization formulation and mechanical a priori assumptions. A phantom experiment was performed to validate the method with optical tracking of deformation as an independent gold standard. RESULTS: There was an excellent agreement between longitudinal strain measured by optical tracking and longitudinal strain measured with TFE velocity encoding. Difference between the two methods was 0.0025 ± 0.085 (ns). Mean global longitudinal strain in the 36 healthy volunteers was −0.18 ± 0.10 (TFE imaging). Intra-observer variability for all segments was 0.00 ± 0.06. Inter-observer variability was −0.02 ± 0.07 (TFE imaging). The intra-observer variability for radial strain was high limiting the applicability of radial strain. Mean longitudinal strain in patients was significantly lower (−0.15± 0.12) compared to healthy volunteers (p<0.05). Strain (expressed as percentage of normal strain) in infarcted regions was lower compared to remote areas (p<0.01). CONCLUSION: In conclusion, we have developed and validated a robust and clinically applicable technique that can quantify longitudinal strain and regional myocardial wall function and present the associated normal values for longitudinal strain. |
format | Online Article Text |
id | pubmed-3562217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35622172013-02-05 Longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study Heiberg, Einar Pahlm-Webb, Ulrika Agarwal, Shruti Bergvall, Erik Fransson, Helen Steding-Ehrenborg, Katarina Carlsson, Marcus Arheden, Håkan J Cardiovasc Magn Reson Research BACKGROUND: Regional myocardial function is typically evaluated by visual assessment by experienced users, or by methods requiring substantial post processing time. Visual assessment is subjective and not quantitative. Therefore, the purpose of this study is to develop and validate a simple method to derive quantitative measures of regional wall function from velocity encoded Cardiovascular Magnetic Resonance (CMR), and provide associated normal values for longitudinal strain. METHOD: Both fast field echo (FFE) and turbo field echo (TFE) velocity encoded CMR images were acquired in three long axis planes in 36 healthy volunteers (13 women, 23 men), age 35±12 years. Strain was also quantified in 10 patients within one week after myocardial infarction. The user manually delineated myocardium in one time frame and strain was calculated as the myocardium was tracked throughout the cardiac cycle using an optimization formulation and mechanical a priori assumptions. A phantom experiment was performed to validate the method with optical tracking of deformation as an independent gold standard. RESULTS: There was an excellent agreement between longitudinal strain measured by optical tracking and longitudinal strain measured with TFE velocity encoding. Difference between the two methods was 0.0025 ± 0.085 (ns). Mean global longitudinal strain in the 36 healthy volunteers was −0.18 ± 0.10 (TFE imaging). Intra-observer variability for all segments was 0.00 ± 0.06. Inter-observer variability was −0.02 ± 0.07 (TFE imaging). The intra-observer variability for radial strain was high limiting the applicability of radial strain. Mean longitudinal strain in patients was significantly lower (−0.15± 0.12) compared to healthy volunteers (p<0.05). Strain (expressed as percentage of normal strain) in infarcted regions was lower compared to remote areas (p<0.01). CONCLUSION: In conclusion, we have developed and validated a robust and clinically applicable technique that can quantify longitudinal strain and regional myocardial wall function and present the associated normal values for longitudinal strain. BioMed Central 2013-01-23 /pmc/articles/PMC3562217/ /pubmed/23343426 http://dx.doi.org/10.1186/1532-429X-15-15 Text en Copyright ©2013 Heiberg et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Heiberg, Einar Pahlm-Webb, Ulrika Agarwal, Shruti Bergvall, Erik Fransson, Helen Steding-Ehrenborg, Katarina Carlsson, Marcus Arheden, Håkan Longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study |
title | Longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study |
title_full | Longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study |
title_fullStr | Longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study |
title_full_unstemmed | Longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study |
title_short | Longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study |
title_sort | longitudinal strain from velocity encoded cardiovascular magnetic resonance: a validation study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3562217/ https://www.ncbi.nlm.nih.gov/pubmed/23343426 http://dx.doi.org/10.1186/1532-429X-15-15 |
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