Evaluation of Deep Learning Estimation of Whole Heart Anatomy from Automated Cardiovascular Magnetic Resonance Short- and Long-Axis Analyses in UK Biobank.
Journal
European heart journal. Cardiovascular Imaging
ISSN: 2047-2412
Titre abrégé: Eur Heart J Cardiovasc Imaging
Pays: England
ID NLM: 101573788
Informations de publication
Date de publication:
09 May 2024
09 May 2024
Historique:
received:
21
02
2024
revised:
10
04
2024
accepted:
25
04
2024
medline:
10
5
2024
pubmed:
10
5
2024
entrez:
9
5
2024
Statut:
aheadofprint
Résumé
Standard methods of heart chamber volume estimation in cardiovascular magnetic resonance (CMR) typically utilize simple geometric formulae based on a limited number of slices. We aimed to evaluate whether an automated deep learning neural network prediction of 3D anatomy of all four chambers would show stronger associations with cardiovascular risk factors and disease than standard volume estimation methods in the UK Biobank. A deep learning network was adapted to predict 3D segmentations of left and right ventricles (LV, RV) and atria (LA, RA) at ∼1mm isotropic resolution from CMR short and long axis 2D segmentations obtained from a fully automated machine learning pipeline in 4723 individuals with cardiovascular disease (CVD) and 5733 without in the UK Biobank. Relationships between volumes at end-diastole (ED) and end-systole (ES) and risk/disease factors were quantified using univariate, multivariate and logistic regression analyses. Strength of association between deep learning volumes and standard volumes was compared using the area under the receiving operator characteristic curve (AUC). Univariate and multivariate associations between deep learning volumes and most risk and disease factors were stronger than for standard volumes (higher R2 and more significant P values), particularly for sex, age, and body mass index. AUC for all logistic regressions were higher for deep learning volumes than standard volumes (p<0.001 for all four chambers at ED and ES). Neural network reconstructions of whole heart volumes had significantly stronger associations with cardiovascular disease and risk factors than standard volume estimation methods in an automatic processing pipeline.
Identifiants
pubmed: 38723059
pii: 7667846
doi: 10.1093/ehjci/jeae123
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.