Identification and Quantification of Cardiovascular Structures From CCTA: An End-to-End, Rapid, Pixel-Wise, Deep-Learning Method.


Journal

JACC. Cardiovascular imaging
ISSN: 1876-7591
Titre abrégé: JACC Cardiovasc Imaging
Pays: United States
ID NLM: 101467978

Informations de publication

Date de publication:
05 2020
Historique:
received: 30 05 2019
revised: 08 08 2019
accepted: 23 08 2019
pubmed: 15 10 2019
medline: 6 1 2021
entrez: 15 10 2019
Statut: ppublish

Résumé

This study designed and evaluated an end-to-end deep learning solution for cardiac segmentation and quantification. Segmentation of cardiac structures from coronary computed tomography angiography (CCTA) images is laborious. We designed an end-to-end deep-learning solution. Scans were obtained from multicenter registries of 166 patients who underwent clinically indicated CCTA. Left ventricular volume (LVV) and right ventricular volume (RVV), left atrial volume (LAV) and right atrial volume (RAV), and left ventricular myocardial mass (LVM) were manually annotated as ground truth. A U-Net-inspired, deep-learning model was trained, validated, and tested in a 70:20:10 split. Mean age was 61.1 ± 8.4 years, and 49% were women. A combined overall median Dice score of 0.9246 (interquartile range: 0.8870 to 0.9475) was achieved. The median Dice scores for LVV, RVV, LAV, RAV, and LVM were 0.938 (interquartile range: 0.887 to 0.958), 0.927 (interquartile range: 0.916 to 0.946), 0.934 (interquartile range: 0.899 to 0.950), 0.915 (interquartile range: 0.890 to 0.920), and 0.920 (interquartile range: 0.811 to 0.944), respectively. Model prediction correlated and agreed well with manual annotation for LVV (r = 0.98), RVV (r = 0.97), LAV (r = 0.78), RAV (r = 0.97), and LVM (r = 0.94) (p < 0.05 for all). Mean difference and limits of agreement for LVV, RVV, LAV, RAV, and LVM were 1.20 ml (95% CI: -7.12 to 9.51), -0.78 ml (95% CI: -10.08 to 8.52), -3.75 ml (95% CI: -21.53 to 14.03), 0.97 ml (95% CI: -6.14 to 8.09), and 6.41 g (95% CI: -8.71 to 21.52), respectively. A deep-learning model rapidly segmented and quantified cardiac structures. This was done with high accuracy on a pixel level, with good agreement with manual annotation, facilitating its expansion into areas of research and clinical import.

Sections du résumé

OBJECTIVES
This study designed and evaluated an end-to-end deep learning solution for cardiac segmentation and quantification.
BACKGROUND
Segmentation of cardiac structures from coronary computed tomography angiography (CCTA) images is laborious. We designed an end-to-end deep-learning solution.
METHODS
Scans were obtained from multicenter registries of 166 patients who underwent clinically indicated CCTA. Left ventricular volume (LVV) and right ventricular volume (RVV), left atrial volume (LAV) and right atrial volume (RAV), and left ventricular myocardial mass (LVM) were manually annotated as ground truth. A U-Net-inspired, deep-learning model was trained, validated, and tested in a 70:20:10 split.
RESULTS
Mean age was 61.1 ± 8.4 years, and 49% were women. A combined overall median Dice score of 0.9246 (interquartile range: 0.8870 to 0.9475) was achieved. The median Dice scores for LVV, RVV, LAV, RAV, and LVM were 0.938 (interquartile range: 0.887 to 0.958), 0.927 (interquartile range: 0.916 to 0.946), 0.934 (interquartile range: 0.899 to 0.950), 0.915 (interquartile range: 0.890 to 0.920), and 0.920 (interquartile range: 0.811 to 0.944), respectively. Model prediction correlated and agreed well with manual annotation for LVV (r = 0.98), RVV (r = 0.97), LAV (r = 0.78), RAV (r = 0.97), and LVM (r = 0.94) (p < 0.05 for all). Mean difference and limits of agreement for LVV, RVV, LAV, RAV, and LVM were 1.20 ml (95% CI: -7.12 to 9.51), -0.78 ml (95% CI: -10.08 to 8.52), -3.75 ml (95% CI: -21.53 to 14.03), 0.97 ml (95% CI: -6.14 to 8.09), and 6.41 g (95% CI: -8.71 to 21.52), respectively.
CONCLUSIONS
A deep-learning model rapidly segmented and quantified cardiac structures. This was done with high accuracy on a pixel level, with good agreement with manual annotation, facilitating its expansion into areas of research and clinical import.

Identifiants

pubmed: 31607673
pii: S1936-878X(19)30873-3
doi: 10.1016/j.jcmg.2019.08.025
pii:
doi:

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1163-1171

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Lohendran Baskaran (L)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York; Department of Radiology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, New York; Department of Cardiovascular Medicine, National Heart Centre, Singapore. Electronic address: lob2008@med.cornell.edu.

Gabriel Maliakal (G)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Subhi J Al'Aref (SJ)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York; Department of Radiology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, New York.

Gurpreet Singh (G)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Zhuoran Xu (Z)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Kelly Michalak (K)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Kristina Dolan (K)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Umberto Gianni (U)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Alexander van Rosendael (A)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Inge van den Hoogen (I)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Donghee Han (D)

Department of Imaging, Cedars-Sinai Medical Center, Cedars-Sinai Heart Institute, Los Angeles, California.

Wijnand Stuijfzand (W)

Department of Cardiology, Amsterdam UMC, Location VU University Medical Center, Amsterdam, the Netherlands.

Mohit Pandey (M)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Benjamin C Lee (BC)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York.

Fay Lin (F)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York; Department of Radiology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, New York.

Gianluca Pontone (G)

Centro Cardiologico Monzino, IRCCS, Milan, Italy.

Paul Knaapen (P)

Department of Cardiology, Amsterdam UMC, Location VU University Medical Center, Amsterdam, the Netherlands.

Hugo Marques (H)

UNICA, Cardiac CT and MRI Unit, Hospital da Luz, Lisbon, Portugal.

Jeroen Bax (J)

Department of Cardiology, Heart Lung Center, Leiden University Medical Center, Leiden, the Netherlands.

Daniel Berman (D)

Department of Imaging, Cedars-Sinai Medical Center, Cedars-Sinai Heart Institute, Los Angeles, California.

Hyuk-Jae Chang (HJ)

Division of Cardiology, Severance Cardiovascular Hospital, Integrative Cardiovascular Imaging Center, Yonsei University College of Medicine, Seoul, South Korea.

Leslee J Shaw (LJ)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York; Department of Radiology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, New York.

James K Min (JK)

Dalio Institute of Cardiovascular Imaging, Weill Cornell Medicine, New York, New York; Department of Radiology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, New York.

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