Machine learning derived segmentation of phase velocity encoded cardiovascular magnetic resonance for fully automated aortic flow quantification.


Journal

Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
ISSN: 1532-429X
Titre abrégé: J Cardiovasc Magn Reson
Pays: England
ID NLM: 9815616

Informations de publication

Date de publication:
07 01 2019
Historique:
received: 29 05 2018
accepted: 18 11 2018
entrez: 8 1 2019
pubmed: 8 1 2019
medline: 20 12 2019
Statut: epublish

Résumé

Phase contrast (PC) cardiovascular magnetic resonance (CMR) is widely employed for flow quantification, but analysis typically requires time consuming manual segmentation which can require human correction. Advances in machine learning have markedly improved automated processing, but have yet to be applied to PC-CMR. This study tested a novel machine learning model for fully automated analysis of PC-CMR aortic flow. A machine learning model was designed to track aortic valve borders based on neural network approaches. The model was trained in a derivation cohort encompassing 150 patients who underwent clinical PC-CMR then compared to manual and commercially-available automated segmentation in a prospective validation cohort. Further validation testing was performed in an external cohort acquired from a different site/CMR vendor. Among 190 coronary artery disease patients prospectively undergoing CMR on commercial scanners (84% 1.5T, 16% 3T), machine learning segmentation was uniformly successful, requiring no human intervention: Segmentation time was < 0.01 min/case (1.2 min for entire dataset); manual segmentation required 3.96 ± 0.36 min/case (12.5 h for entire dataset). Correlations between machine learning and manual segmentation-derived flow approached unity (r = 0.99, p < 0.001). Machine learning yielded smaller absolute differences with manual segmentation than did commercial automation (1.85 ± 1.80 vs. 3.33 ± 3.18 mL, p < 0.01): Nearly all (98%) of cases differed by ≤5 mL between machine learning and manual methods. Among patients without advanced mitral regurgitation, machine learning correlated well (r = 0.63, p < 0.001) and yielded small differences with cine-CMR stroke volume (∆ 1.3 ± 17.7 mL, p = 0.36). Among advanced mitral regurgitation patients, machine learning yielded lower stroke volume than did volumetric cine-CMR (∆ 12.6 ± 20.9 mL, p = 0.005), further supporting validity of this method. Among the external validation cohort (n = 80) acquired using a different CMR vendor, the algorithm yielded equivalently small differences (∆ 1.39 ± 1.77 mL, p = 0.4) and high correlations (r = 0.99, p < 0.001) with manual segmentation, including similar results in 20 patients with bicuspid or stenotic aortic valve pathology (∆ 1.71 ± 2.25 mL, p = 0.25). Fully automated machine learning PC-CMR segmentation performs robustly for aortic flow quantification - yielding rapid segmentation, small differences with manual segmentation, and identification of differential forward/left ventricular volumetric stroke volume in context of concomitant mitral regurgitation. Findings support use of machine learning for analysis of large scale CMR datasets.

Sections du résumé

BACKGROUND
Phase contrast (PC) cardiovascular magnetic resonance (CMR) is widely employed for flow quantification, but analysis typically requires time consuming manual segmentation which can require human correction. Advances in machine learning have markedly improved automated processing, but have yet to be applied to PC-CMR. This study tested a novel machine learning model for fully automated analysis of PC-CMR aortic flow.
METHODS
A machine learning model was designed to track aortic valve borders based on neural network approaches. The model was trained in a derivation cohort encompassing 150 patients who underwent clinical PC-CMR then compared to manual and commercially-available automated segmentation in a prospective validation cohort. Further validation testing was performed in an external cohort acquired from a different site/CMR vendor.
RESULTS
Among 190 coronary artery disease patients prospectively undergoing CMR on commercial scanners (84% 1.5T, 16% 3T), machine learning segmentation was uniformly successful, requiring no human intervention: Segmentation time was < 0.01 min/case (1.2 min for entire dataset); manual segmentation required 3.96 ± 0.36 min/case (12.5 h for entire dataset). Correlations between machine learning and manual segmentation-derived flow approached unity (r = 0.99, p < 0.001). Machine learning yielded smaller absolute differences with manual segmentation than did commercial automation (1.85 ± 1.80 vs. 3.33 ± 3.18 mL, p < 0.01): Nearly all (98%) of cases differed by ≤5 mL between machine learning and manual methods. Among patients without advanced mitral regurgitation, machine learning correlated well (r = 0.63, p < 0.001) and yielded small differences with cine-CMR stroke volume (∆ 1.3 ± 17.7 mL, p = 0.36). Among advanced mitral regurgitation patients, machine learning yielded lower stroke volume than did volumetric cine-CMR (∆ 12.6 ± 20.9 mL, p = 0.005), further supporting validity of this method. Among the external validation cohort (n = 80) acquired using a different CMR vendor, the algorithm yielded equivalently small differences (∆ 1.39 ± 1.77 mL, p = 0.4) and high correlations (r = 0.99, p < 0.001) with manual segmentation, including similar results in 20 patients with bicuspid or stenotic aortic valve pathology (∆ 1.71 ± 2.25 mL, p = 0.25).
CONCLUSION
Fully automated machine learning PC-CMR segmentation performs robustly for aortic flow quantification - yielding rapid segmentation, small differences with manual segmentation, and identification of differential forward/left ventricular volumetric stroke volume in context of concomitant mitral regurgitation. Findings support use of machine learning for analysis of large scale CMR datasets.

Identifiants

pubmed: 30612574
doi: 10.1186/s12968-018-0509-0
pii: 10.1186/s12968-018-0509-0
pmc: PMC6322266
doi:

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL102249
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL140092
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL128278
Pays : United States

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Auteurs

Alex Bratt (A)

Department of Radiology, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Jiwon Kim (J)

Department of Radiology, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.
Greenberg Division of Cardiology, Department of Medicine, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Meridith Pollie (M)

Greenberg Division of Cardiology, Department of Medicine, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Ashley N Beecy (AN)

Greenberg Division of Cardiology, Department of Medicine, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Nathan H Tehrani (NH)

Greenberg Division of Cardiology, Department of Medicine, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Noel Codella (N)

IBM TJ Watson Research Center, 1101 Kitchawan Rd, Yorktown Heights, NY, 10598, USA.

Rocio Perez-Johnston (R)

Memorial Sloan Kettering Cancer Center, 1275 York Ave, New York, NY, 10065, USA.

Maria Chiara Palumbo (MC)

Greenberg Division of Cardiology, Department of Medicine, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Javid Alakbarli (J)

Greenberg Division of Cardiology, Department of Medicine, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Wayne Colizza (W)

Department of Radiology, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Ian R Drexler (IR)

Department of Radiology, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Clerio F Azevedo (CF)

Duke Cardiovascular Magnetic Resonance Center, 10 Duke Medicine Circle, Durham, NC, 27710, USA.

Raymond J Kim (RJ)

Duke Cardiovascular Magnetic Resonance Center, 10 Duke Medicine Circle, Durham, NC, 27710, USA.

Richard B Devereux (RB)

Greenberg Division of Cardiology, Department of Medicine, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA.

Jonathan W Weinsaft (JW)

Department of Radiology, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA. jww2001@med.cornell.edu.
Greenberg Division of Cardiology, Department of Medicine, Weill Cornell Medicine, 525 E 68th St, New York, NY, 10065, USA. jww2001@med.cornell.edu.
Memorial Sloan Kettering Cancer Center, 1275 York Ave, New York, NY, 10065, USA. jww2001@med.cornell.edu.
Weill Cornell Medical College, 525 East 68th Street, New York, NY, 10021, USA. jww2001@med.cornell.edu.

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Classifications MeSH