Cargando…
3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation
BACKGROUND: Image-domain motion correction of black-blood contrast T2-weighted fetal cardiovascular magnetic resonance imaging (CMR) using slice-to-volume registration (SVR) provides high-resolution three-dimensional (3D) images of the fetal heart providing excellent 3D visualisation of vascular ano...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753334/ https://www.ncbi.nlm.nih.gov/pubmed/36517850 http://dx.doi.org/10.1186/s12968-022-00902-z |
_version_ | 1784850941684482048 |
---|---|
author | Uus, Alena U. van Poppel, Milou P. M. Steinweg, Johannes K. Grigorescu, Irina Ramirez Gilliland, Paula Roberts, Thomas A. Egloff Collado, Alexia Rutherford, Mary A. Hajnal, Joseph V. Lloyd, David F. A. Pushparajah, Kuberan Deprez, Maria |
author_facet | Uus, Alena U. van Poppel, Milou P. M. Steinweg, Johannes K. Grigorescu, Irina Ramirez Gilliland, Paula Roberts, Thomas A. Egloff Collado, Alexia Rutherford, Mary A. Hajnal, Joseph V. Lloyd, David F. A. Pushparajah, Kuberan Deprez, Maria |
author_sort | Uus, Alena U. |
collection | PubMed |
description | BACKGROUND: Image-domain motion correction of black-blood contrast T2-weighted fetal cardiovascular magnetic resonance imaging (CMR) using slice-to-volume registration (SVR) provides high-resolution three-dimensional (3D) images of the fetal heart providing excellent 3D visualisation of vascular anomalies [1]. However, 3D segmentation of these datasets, important for both clinical reporting and the application of advanced analysis techniques is currently a time-consuming process requiring manual input with potential for inter-user variability. METHODS: In this work, we present novel 3D fetal CMR population-averaged atlases of normal and abnormal fetal cardiovascular anatomy. The atlases are created using motion-corrected 3D reconstructed volumes of 86 third trimester fetuses (gestational age range 29-34 weeks) including: 28 healthy controls, 20 cases with postnatally confirmed neonatal coarctation of the aorta (CoA) and 38 vascular rings (21 right aortic arch (RAA), 17 double aortic arch (DAA)). We used only high image quality datasets with isolated anomalies and without any other deviations in the cardiovascular anatomy.In addition, we implemented and evaluated atlas-guided registration and deep learning (UNETR) methods for automated 3D multi-label segmentation of fetal cardiac vessels. We used images from CoA, RAA and DAA cohorts including: 42 cases for training (14 from each cohort), 3 for validation and 6 for testing. In addition, the potential limitations of the network were investigated on unseen datasets including 3 early gestational age (22 weeks) and 3 low SNR cases. RESULTS: We created four atlases representing the average anatomy of the normal fetal heart, postnatally confirmed neonatal CoA, RAA and DAA. Visual inspection was undertaken to verify expected anatomy per subgroup. The results of the multi-label cardiac vessel UNETR segmentation showed 100[Formula: see text] per-vessel detection rate for both normal and abnormal aortic arch anatomy. CONCLUSIONS: This work introduces the first set of 3D black-blood T2-weighted CMR atlases of normal and abnormal fetal cardiovascular anatomy including detailed segmentation of the major cardiovascular structures. Additionally, we demonstrated the general feasibility of using deep learning for multi-label vessel segmentation of 3D fetal CMR images. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12968-022-00902-z. |
format | Online Article Text |
id | pubmed-9753334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97533342022-12-16 3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation Uus, Alena U. van Poppel, Milou P. M. Steinweg, Johannes K. Grigorescu, Irina Ramirez Gilliland, Paula Roberts, Thomas A. Egloff Collado, Alexia Rutherford, Mary A. Hajnal, Joseph V. Lloyd, David F. A. Pushparajah, Kuberan Deprez, Maria J Cardiovasc Magn Reson Research BACKGROUND: Image-domain motion correction of black-blood contrast T2-weighted fetal cardiovascular magnetic resonance imaging (CMR) using slice-to-volume registration (SVR) provides high-resolution three-dimensional (3D) images of the fetal heart providing excellent 3D visualisation of vascular anomalies [1]. However, 3D segmentation of these datasets, important for both clinical reporting and the application of advanced analysis techniques is currently a time-consuming process requiring manual input with potential for inter-user variability. METHODS: In this work, we present novel 3D fetal CMR population-averaged atlases of normal and abnormal fetal cardiovascular anatomy. The atlases are created using motion-corrected 3D reconstructed volumes of 86 third trimester fetuses (gestational age range 29-34 weeks) including: 28 healthy controls, 20 cases with postnatally confirmed neonatal coarctation of the aorta (CoA) and 38 vascular rings (21 right aortic arch (RAA), 17 double aortic arch (DAA)). We used only high image quality datasets with isolated anomalies and without any other deviations in the cardiovascular anatomy.In addition, we implemented and evaluated atlas-guided registration and deep learning (UNETR) methods for automated 3D multi-label segmentation of fetal cardiac vessels. We used images from CoA, RAA and DAA cohorts including: 42 cases for training (14 from each cohort), 3 for validation and 6 for testing. In addition, the potential limitations of the network were investigated on unseen datasets including 3 early gestational age (22 weeks) and 3 low SNR cases. RESULTS: We created four atlases representing the average anatomy of the normal fetal heart, postnatally confirmed neonatal CoA, RAA and DAA. Visual inspection was undertaken to verify expected anatomy per subgroup. The results of the multi-label cardiac vessel UNETR segmentation showed 100[Formula: see text] per-vessel detection rate for both normal and abnormal aortic arch anatomy. CONCLUSIONS: This work introduces the first set of 3D black-blood T2-weighted CMR atlases of normal and abnormal fetal cardiovascular anatomy including detailed segmentation of the major cardiovascular structures. Additionally, we demonstrated the general feasibility of using deep learning for multi-label vessel segmentation of 3D fetal CMR images. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12968-022-00902-z. BioMed Central 2022-12-15 /pmc/articles/PMC9753334/ /pubmed/36517850 http://dx.doi.org/10.1186/s12968-022-00902-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Uus, Alena U. van Poppel, Milou P. M. Steinweg, Johannes K. Grigorescu, Irina Ramirez Gilliland, Paula Roberts, Thomas A. Egloff Collado, Alexia Rutherford, Mary A. Hajnal, Joseph V. Lloyd, David F. A. Pushparajah, Kuberan Deprez, Maria 3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation |
title | 3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation |
title_full | 3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation |
title_fullStr | 3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation |
title_full_unstemmed | 3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation |
title_short | 3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation |
title_sort | 3d black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753334/ https://www.ncbi.nlm.nih.gov/pubmed/36517850 http://dx.doi.org/10.1186/s12968-022-00902-z |
work_keys_str_mv | AT uusalenau 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT vanpoppelmiloupm 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT steinwegjohannesk 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT grigorescuirina 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT ramirezgillilandpaula 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT robertsthomasa 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT egloffcolladoalexia 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT rutherfordmarya 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT hajnaljosephv 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT lloyddavidfa 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT pushparajahkuberan 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation AT deprezmaria 3dblackbloodcardiovascularmagneticresonanceatlasesofcongenitalaorticarchanomaliesandthenormalfetalheartapplicationtoautomatedmultilabelsegmentation |