Accurate diagnosis of apical hypertrophic cardiomyopathy using explainable advanced electrocardiogram analysis

Author:

Hughes Rebecca K12ORCID,Thornton George D12ORCID,Malcolmson James W23ORCID,Pierce Iain2ORCID,Khoury Shafik4ORCID,Hornell Amanda5ORCID,Knott Kristopher12ORCID,Captur Gabriella167ORCID,Moon James C12ORCID,Schlegel Todd T58ORCID,Ugander Martin59ORCID

Affiliation:

1. Institute of Cardiovascular Science, University College London , Gower Street, London , UK

2. Barts Heart Centre, The Cardiovascular Magnetic Resonance Imaging Unit and The Inherited Cardiovascular Diseases Unit, St Bartholomew’s Hospital , West Smithfield, London , UK

3. William Harvey Institute, Queen Mary University of London , London , UK

4. Cardiovascular Clinical and Academic Group, Molecular and Clinical Sciences Institute, St George’s University of London , London , UK

5. Department of Clinical Physiology, Karolinska University Hospital and Karolinska Institutet , SE-171-76, Stockholm , Sweden

6. MRC Unit of Lifelong Health and Ageing, University College London , 1-19 Torrington Place, Fitzrovia, London , UK

7. Inherited Heart Muscle Conditions Clinic, Department of Cardiology, Royal Free Hospital, NHS Trust , Gower Street, London , UK

8. Nicollier-Schlegel SARL , Trelex , Switzerland

9. Kolling Institute, Royal North Shore Hospital and University of Sydney, St Leonards, Sydney, NSW 2065 , Australia

Abstract

Abstract Aims Typical electrocardiogram (ECG) features of apical hypertrophic cardiomyopathy (ApHCM) include tall R waves and deep or giant T-wave inversion in the precordial leads, but these features are not always present. The ECG is used as the gatekeeper to cardiac imaging for diagnosis. We tested whether explainable advanced ECG (A-ECG) could accurately diagnose ApHCM. Methods and results Advanced ECG analysis was performed on standard resting 12-lead ECGs in patients with ApHCM [n = 75 overt, n = 32 relative (<15 mm hypertrophy); a subgroup of which underwent cardiovascular magnetic resonance (n = 92)], and comparator subjects (n = 2449), including healthy volunteers (n = 1672), patients with coronary artery disease (n = 372), left ventricular electrical remodelling (n = 108), ischaemic (n = 114) or non-ischaemic cardiomyopathy (n = 57), and asymmetrical septal hypertrophy HCM (n = 126). Multivariable logistic regression identified four A-ECG measures that together discriminated ApHCM from other diseases with high accuracy [area under the receiver operating characteristic (AUC) curve (bootstrapped 95% confidence interval) 0.982 (0.965–0.993)]. Linear discriminant analysis also diagnosed ApHCM with high accuracy [AUC 0.989 (0.986–0.991)]. Conclusion Explainable A-ECG has excellent diagnostic accuracy for ApHCM, even when the hypertrophy is relative, with A-ECG analysis providing incremental diagnostic value over imaging alone. The electrical (ECG) and anatomical (wall thickness) disease features do not completely align, suggesting that future diagnostic and management strategies may incorporate both features.

Funder

British Heart Foundation

National Institute of Health Research Clinical Doctoral Research Fellowship

National Institute for Health Research Rare Diseases Translational Research Collaboration

NIHR University College London Hospitals Biomedical Research Centre

University College London Hospitals NIHR Biomedical Research Centre and Biomedical Research Unit at Barts Hospital

New South Wales Health

Heart Research Australia

University of Sydney

Publisher

Oxford University Press (OUP)

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