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3D Fusion Framework for Infarction and Angiogenesis Analysis in a Myocardial Infarct Minipig Model
The combination of different modality images can provide detailed and comprehensive information for the prognostic assessment and therapeutic strategy of patients with ischemic heart disease. In this study, a 3D fusion framework is designed to integrate coronary computed tomography (CT) angiography...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470135/ https://www.ncbi.nlm.nih.gov/pubmed/28654385 http://dx.doi.org/10.1177/1536012117708735 |
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author | Zhenzhen, Xu Tao, Bo Li, Yu Zhang, Jun Qu, Xiaochao Cao, Feng Liang, Jimin |
author_facet | Zhenzhen, Xu Tao, Bo Li, Yu Zhang, Jun Qu, Xiaochao Cao, Feng Liang, Jimin |
author_sort | Zhenzhen, Xu |
collection | PubMed |
description | The combination of different modality images can provide detailed and comprehensive information for the prognostic assessment and therapeutic strategy of patients with ischemic heart disease. In this study, a 3D fusion framework is designed to integrate coronary computed tomography (CT) angiography (CTA), 2-deoxy-2-[(18)F]fluoro-D-glucose ([(18)F]DG) positron emission tomography (PET)/CT, and [(68)Ga]-1,4,7-triazacyclononane-1,4,7-triacetic acid-(Arg-Gly-Asp)2 ([(68)Ga]-NOTA-PRGD2) PET/CT images of the myocardial infarction model in minipigs. First, the structural anatomy of the heart in coronary CTA and CT is segmented using a multi-atlas-based method. Then, the hearts are registered using the B-spline-based free form deformation. Finally, the [(18)F]DG and [(68)Ga]-NOTA-PRGD2 signals are mapped into the heart in coronary CTA, which produces a single fusion image to delineate both the cardiac structural anatomy and the functional information of myocardial viability and angiogenesis. Heart segmentation demonstrates high accuracy with good agreement between manual delineation and automatic segmentation. The fusion result intuitively reflects the extent of the [(18)F]DG uptake defect as well as the location where the [(68)Ga]-NOTA-PRGD2 signal appears. The fusion result verified the occurrence of angiogenesis based on the in vivo noninvasive molecular imaging approach. The presented framework is helpful in facilitating the study of the relationship between infarct territories and blocked coronary arteries as well as angiogenesis. |
format | Online Article Text |
id | pubmed-5470135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-54701352017-06-22 3D Fusion Framework for Infarction and Angiogenesis Analysis in a Myocardial Infarct Minipig Model Zhenzhen, Xu Tao, Bo Li, Yu Zhang, Jun Qu, Xiaochao Cao, Feng Liang, Jimin Mol Imaging Research Article The combination of different modality images can provide detailed and comprehensive information for the prognostic assessment and therapeutic strategy of patients with ischemic heart disease. In this study, a 3D fusion framework is designed to integrate coronary computed tomography (CT) angiography (CTA), 2-deoxy-2-[(18)F]fluoro-D-glucose ([(18)F]DG) positron emission tomography (PET)/CT, and [(68)Ga]-1,4,7-triazacyclononane-1,4,7-triacetic acid-(Arg-Gly-Asp)2 ([(68)Ga]-NOTA-PRGD2) PET/CT images of the myocardial infarction model in minipigs. First, the structural anatomy of the heart in coronary CTA and CT is segmented using a multi-atlas-based method. Then, the hearts are registered using the B-spline-based free form deformation. Finally, the [(18)F]DG and [(68)Ga]-NOTA-PRGD2 signals are mapped into the heart in coronary CTA, which produces a single fusion image to delineate both the cardiac structural anatomy and the functional information of myocardial viability and angiogenesis. Heart segmentation demonstrates high accuracy with good agreement between manual delineation and automatic segmentation. The fusion result intuitively reflects the extent of the [(18)F]DG uptake defect as well as the location where the [(68)Ga]-NOTA-PRGD2 signal appears. The fusion result verified the occurrence of angiogenesis based on the in vivo noninvasive molecular imaging approach. The presented framework is helpful in facilitating the study of the relationship between infarct territories and blocked coronary arteries as well as angiogenesis. SAGE Publications 2017-05-11 /pmc/articles/PMC5470135/ /pubmed/28654385 http://dx.doi.org/10.1177/1536012117708735 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Zhenzhen, Xu Tao, Bo Li, Yu Zhang, Jun Qu, Xiaochao Cao, Feng Liang, Jimin 3D Fusion Framework for Infarction and Angiogenesis Analysis in a Myocardial Infarct Minipig Model |
title | 3D Fusion Framework for Infarction and Angiogenesis Analysis in a Myocardial Infarct Minipig Model |
title_full | 3D Fusion Framework for Infarction and Angiogenesis Analysis in a Myocardial Infarct Minipig Model |
title_fullStr | 3D Fusion Framework for Infarction and Angiogenesis Analysis in a Myocardial Infarct Minipig Model |
title_full_unstemmed | 3D Fusion Framework for Infarction and Angiogenesis Analysis in a Myocardial Infarct Minipig Model |
title_short | 3D Fusion Framework for Infarction and Angiogenesis Analysis in a Myocardial Infarct Minipig Model |
title_sort | 3d fusion framework for infarction and angiogenesis analysis in a myocardial infarct minipig model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470135/ https://www.ncbi.nlm.nih.gov/pubmed/28654385 http://dx.doi.org/10.1177/1536012117708735 |
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