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Variability of myocardial perfusion dark rim Gibbs artifacts due to sub-pixel shifts

BACKGROUND: Gibbs ringing has been shown as a possible source of dark rim artifacts in myocardial perfusion studies. This type of artifact is usually described as transient, lasting a few heart beats, and localised in random segments of the myocardial wall. Dark rim artifacts are known to be unpredi...

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Autores principales: Ferreira, Pedro, Gatehouse, Peter, Kellman, Peter, Bucciarelli-Ducci, Chiara, Firmin, David
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693509/
https://www.ncbi.nlm.nih.gov/pubmed/19473492
http://dx.doi.org/10.1186/1532-429X-11-17
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author Ferreira, Pedro
Gatehouse, Peter
Kellman, Peter
Bucciarelli-Ducci, Chiara
Firmin, David
author_facet Ferreira, Pedro
Gatehouse, Peter
Kellman, Peter
Bucciarelli-Ducci, Chiara
Firmin, David
author_sort Ferreira, Pedro
collection PubMed
description BACKGROUND: Gibbs ringing has been shown as a possible source of dark rim artifacts in myocardial perfusion studies. This type of artifact is usually described as transient, lasting a few heart beats, and localised in random segments of the myocardial wall. Dark rim artifacts are known to be unpredictably variable. This article aims to illustrate that a sub-pixel shift, i.e. a small displacement of the pixels with respect to the endocardial border, can result in different Gibbs ringing and hence different artifacts. Therefore a hypothesis for one cause of dark rim artifact variability is given based on the sub-pixel position of the endocardial border. This article also demonstrates the consequences for Gibbs artifacts when two different methods of image interpolation are applied (post-FFT interpolation, and pre-FFT zero-filling). RESULTS: Sub-pixel shifting of in vivo perfusion studies was shown to change the appearance of Gibbs artifacts. This effect was visible in the original uninterpolated images, and in the post-FFT interpolated images. The same shifted data interpolated by pre-FFT zero-filling exhibited much less variability in the Gibbs artifact. The in vivo findings were confirmed by phantom imaging and numerical simulations. CONCLUSION: Unless pre-FFT zero-filling interpolation is performed, Gibbs artifacts are very dependent on the position of the subendocardial wall within the pixel. By introducing sub-pixel shifts relative to the endocardial border, some of the variability of the dark rim artifacts in different myocardial segments, in different patients and from frame to frame during first-pass perfusion due to cardiac and respiratory motion can be explained. Image interpolation by zero-filling can be used to minimize this dependency.
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spelling pubmed-26935092009-06-08 Variability of myocardial perfusion dark rim Gibbs artifacts due to sub-pixel shifts Ferreira, Pedro Gatehouse, Peter Kellman, Peter Bucciarelli-Ducci, Chiara Firmin, David J Cardiovasc Magn Reson Research BACKGROUND: Gibbs ringing has been shown as a possible source of dark rim artifacts in myocardial perfusion studies. This type of artifact is usually described as transient, lasting a few heart beats, and localised in random segments of the myocardial wall. Dark rim artifacts are known to be unpredictably variable. This article aims to illustrate that a sub-pixel shift, i.e. a small displacement of the pixels with respect to the endocardial border, can result in different Gibbs ringing and hence different artifacts. Therefore a hypothesis for one cause of dark rim artifact variability is given based on the sub-pixel position of the endocardial border. This article also demonstrates the consequences for Gibbs artifacts when two different methods of image interpolation are applied (post-FFT interpolation, and pre-FFT zero-filling). RESULTS: Sub-pixel shifting of in vivo perfusion studies was shown to change the appearance of Gibbs artifacts. This effect was visible in the original uninterpolated images, and in the post-FFT interpolated images. The same shifted data interpolated by pre-FFT zero-filling exhibited much less variability in the Gibbs artifact. The in vivo findings were confirmed by phantom imaging and numerical simulations. CONCLUSION: Unless pre-FFT zero-filling interpolation is performed, Gibbs artifacts are very dependent on the position of the subendocardial wall within the pixel. By introducing sub-pixel shifts relative to the endocardial border, some of the variability of the dark rim artifacts in different myocardial segments, in different patients and from frame to frame during first-pass perfusion due to cardiac and respiratory motion can be explained. Image interpolation by zero-filling can be used to minimize this dependency. BioMed Central 2009-05-27 /pmc/articles/PMC2693509/ /pubmed/19473492 http://dx.doi.org/10.1186/1532-429X-11-17 Text en Copyright © 2009 Ferreira 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
Ferreira, Pedro
Gatehouse, Peter
Kellman, Peter
Bucciarelli-Ducci, Chiara
Firmin, David
Variability of myocardial perfusion dark rim Gibbs artifacts due to sub-pixel shifts
title Variability of myocardial perfusion dark rim Gibbs artifacts due to sub-pixel shifts
title_full Variability of myocardial perfusion dark rim Gibbs artifacts due to sub-pixel shifts
title_fullStr Variability of myocardial perfusion dark rim Gibbs artifacts due to sub-pixel shifts
title_full_unstemmed Variability of myocardial perfusion dark rim Gibbs artifacts due to sub-pixel shifts
title_short Variability of myocardial perfusion dark rim Gibbs artifacts due to sub-pixel shifts
title_sort variability of myocardial perfusion dark rim gibbs artifacts due to sub-pixel shifts
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693509/
https://www.ncbi.nlm.nih.gov/pubmed/19473492
http://dx.doi.org/10.1186/1532-429X-11-17
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