Development and validation of AI-derived segmentation of four-chamber cine cardiac magnetic resonance.


Journal

European radiology experimental
ISSN: 2509-9280
Titre abrégé: Eur Radiol Exp
Pays: England
ID NLM: 101721752

Informations de publication

Date de publication:
12 Jul 2024
Historique:
received: 13 02 2024
accepted: 30 04 2024
medline: 12 7 2024
pubmed: 12 7 2024
entrez: 11 7 2024
Statut: epublish

Résumé

Cardiac magnetic resonance (CMR) in the four-chamber plane offers comprehensive insight into the volumetrics of the heart. We aimed to develop an artificial intelligence (AI) model of time-resolved segmentation using the four-chamber cine. A fully automated deep learning algorithm was trained using retrospective multicentre and multivendor data of 814 subjects. Validation, reproducibility, and mortality prediction were evaluated on an independent cohort of 101 subjects. The mean age of the validation cohort was 54 years, and 66 (65%) were males. Left and right heart parameters demonstrated strong correlations between automated and manual analysis, with a ρ of 0.91-0.98 and 0.89-0.98, respectively, with minimal bias. All AI four-chamber volumetrics in repeatability analysis demonstrated high correlation (ρ = 0.99-1.00) and no bias. Automated four-chamber analysis underestimated both left ventricular (LV) and right ventricular (RV) volumes compared to ground-truth short-axis cine analysis. Two correction factors for LV and RV four-chamber analysis were proposed based on systematic bias. After applying the correction factors, a strong correlation and minimal bias for LV volumetrics were observed. During a mean follow-up period of 6.75 years, 16 patients died. On stepwise multivariable analysis, left atrial ejection fraction demonstrated an independent association with death in both manual (hazard ratio (HR) = 0.96, p = 0.003) and AI analyses (HR = 0.96, p < 0.001). Fully automated four-chamber CMR is feasible, reproducible, and has the same real-world prognostic value as manual analysis. LV volumes by four-chamber segmentation were comparable to short-axis volumetric assessment. ClinicalTrials.gov: NCT05114785. Integrating fully automated AI in CMR promises to revolutionise clinical cardiac assessment, offering efficient, accurate, and prognostically valuable insights for improved patient care and outcomes. • Four-chamber cine sequences remain one of the most informative acquisitions in CMR examination. • This deep learning-based, time-resolved, fully automated four-chamber volumetric, functional, and deformation analysis solution. • LV and RV were underestimated by four-chamber analysis compared to ground truth short-axis segmentation. • Correction bias for both LV and RV volumes by four-chamber segmentation, minimises the systematic bias.

Sections du résumé

BACKGROUND BACKGROUND
Cardiac magnetic resonance (CMR) in the four-chamber plane offers comprehensive insight into the volumetrics of the heart. We aimed to develop an artificial intelligence (AI) model of time-resolved segmentation using the four-chamber cine.
METHODS METHODS
A fully automated deep learning algorithm was trained using retrospective multicentre and multivendor data of 814 subjects. Validation, reproducibility, and mortality prediction were evaluated on an independent cohort of 101 subjects.
RESULTS RESULTS
The mean age of the validation cohort was 54 years, and 66 (65%) were males. Left and right heart parameters demonstrated strong correlations between automated and manual analysis, with a ρ of 0.91-0.98 and 0.89-0.98, respectively, with minimal bias. All AI four-chamber volumetrics in repeatability analysis demonstrated high correlation (ρ = 0.99-1.00) and no bias. Automated four-chamber analysis underestimated both left ventricular (LV) and right ventricular (RV) volumes compared to ground-truth short-axis cine analysis. Two correction factors for LV and RV four-chamber analysis were proposed based on systematic bias. After applying the correction factors, a strong correlation and minimal bias for LV volumetrics were observed. During a mean follow-up period of 6.75 years, 16 patients died. On stepwise multivariable analysis, left atrial ejection fraction demonstrated an independent association with death in both manual (hazard ratio (HR) = 0.96, p = 0.003) and AI analyses (HR = 0.96, p < 0.001).
CONCLUSION CONCLUSIONS
Fully automated four-chamber CMR is feasible, reproducible, and has the same real-world prognostic value as manual analysis. LV volumes by four-chamber segmentation were comparable to short-axis volumetric assessment.
TRIALS REGISTRATION BACKGROUND
ClinicalTrials.gov: NCT05114785.
RELEVANCE STATEMENT CONCLUSIONS
Integrating fully automated AI in CMR promises to revolutionise clinical cardiac assessment, offering efficient, accurate, and prognostically valuable insights for improved patient care and outcomes.
KEY POINTS CONCLUSIONS
• Four-chamber cine sequences remain one of the most informative acquisitions in CMR examination. • This deep learning-based, time-resolved, fully automated four-chamber volumetric, functional, and deformation analysis solution. • LV and RV were underestimated by four-chamber analysis compared to ground truth short-axis segmentation. • Correction bias for both LV and RV volumes by four-chamber segmentation, minimises the systematic bias.

Identifiants

pubmed: 38992116
doi: 10.1186/s41747-024-00477-7
pii: 10.1186/s41747-024-00477-7
doi:

Banques de données

ClinicalTrials.gov
['NCT05114785']

Types de publication

Journal Article Validation Study Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

77

Subventions

Organisme : Wellcome Trust
ID : 220703/Z/20/Z
Pays : United Kingdom

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Hosamadin Assadi (H)

Department of Cardiovascular and Metabolic Health, Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK.
Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Samer Alabed (S)

Department of Infection, Immunity & Cardiovascular Disease, University of Sheffield, Sheffield, UK.

Rui Li (R)

Department of Cardiovascular and Metabolic Health, Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK.
Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Gareth Matthews (G)

Department of Cardiovascular and Metabolic Health, Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK.
Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Kavita Karunasaagarar (K)

Department of Infection, Immunity & Cardiovascular Disease, University of Sheffield, Sheffield, UK.

Bahman Kasmai (B)

Department of Cardiovascular and Metabolic Health, Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK.
Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Sunil Nair (S)

Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Zia Mehmood (Z)

Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Ciaran Grafton-Clarke (C)

Department of Cardiovascular and Metabolic Health, Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK.
Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Peter P Swoboda (PP)

Division of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Andrew J Swift (AJ)

Department of Infection, Immunity & Cardiovascular Disease, University of Sheffield, Sheffield, UK.

John P Greenwood (JP)

Division of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Vassilios S Vassiliou (VS)

Department of Cardiovascular and Metabolic Health, Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK.
Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK.

Sven Plein (S)

Division of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Rob J van der Geest (RJ)

Department of Radiology, Division of Image Processing, Leiden University Medical Center, Leiden, The Netherlands.

Pankaj Garg (P)

Department of Cardiovascular and Metabolic Health, Norwich Medical School, University of East Anglia, Norwich, Norfolk, UK. P.Garg@uea.ac.uk.
Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, Norfolk, UK. P.Garg@uea.ac.uk.

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