Ventricular volume asymmetry as a novel imaging biomarker for disease discrimination and outcome prediction

Author:

McCracken Celeste1,Szabo Liliana234ORCID,Abdulelah Zaid A2,Condurache Dorina-Gabriela23ORCID,Vago Hajnalka45,Nichols Thomas E678,Petersen Steffen E239,Neubauer Stefan1ORCID,Raisi-Estabragh Zahra23ORCID

Affiliation:

1. Division of Cardiovascular Medicine, Oxford Centre for Clinical Magnetic Resonance Research, Radcliffe Department of Medicine, University of Oxford, National Institute for Health Research Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust , Oxford OX3 9DU , UK

2. Barts Heart Centre, St Bartholomew’s Hospital, Barts Health NHS Trust , West Smithfield, London EC1A 7BE , UK

3. William Harvey Research Institute, NIHR Barts Biomedical Research Centre, Queen Mary University of London , Charterhouse Square, London EC1M 6BQ , UK

4. Heart and Vascular Center, Semmelweis University , Budapest 1122 , Hungary

5. Department of Sports Medicine, Semmelweis University , Budapest 1085 , Hungary

6. Wellcome Centre for Integrative Neuroimaging (WIN FMRIB), University of Oxford , Oxford OX3 9DA , UK

7. Big Data Institute, University of Oxford , Oxford OX3 7LF , UK

8. Nuffield Department Population Health, Big Data Institute, University of Oxford , Oxford OX3 7LF , UK

9. Health Data Research UK , London NW1 2BE , UK

Abstract

Abstract Aims Disruption of the predictable symmetry of the healthy heart may be an indicator of cardiovascular risk. This study defines the population distribution of ventricular asymmetry and its relationships across a range of prevalent and incident cardiorespiratory diseases. Methods and results The analysis includes 44 796 UK Biobank participants (average age 64.1 ± 7.7 years; 51.9% women). Cardiovascular magnetic resonance (CMR) metrics were derived using previously validated automated pipelines. Ventricular asymmetry was expressed as the ratio of left and right ventricular (LV and RV) end-diastolic volumes. Clinical outcomes were defined through linked health records. Incident events were those occurring for the first time after imaging, longitudinally tracked over an average follow-up time of 4.75 ± 1.52 years. The normal range for ventricular symmetry was defined in a healthy subset. Participants with values outside the 5th-95th percentiles of the healthy distribution were classed as either LV dominant (LV/RV > 112%) or RV dominant (LV/RV < 80%) asymmetry. Associations of LV and RV dominant asymmetry with vascular risk factors, CMR features, and prevalent and incident cardiovascular diseases (CVDs) were examined using regression models, adjusting for vascular risk factors, prevalent diseases, and conventional CMR measures. Left ventricular dominance was linked to an array of pre-existing vascular risk factors and CVDs, and a two-fold increased risk of incident heart failure, non-ischaemic cardiomyopathies, and left-sided valvular disorders. Right ventricular dominance was associated with an elevated risk of all-cause mortality. Conclusion Ventricular asymmetry has clinical utility for cardiovascular risk assessment, providing information that is incremental to traditional risk factors and conventional CMR metrics.

Funder

Barts Charity

UK Biobank

Oxford NIHR Biomedical Research Centre

Oxford British Heart Foundation Centre of Research Excellence

National Institute for Health and Care Research

Integrated Academic Training programme

Academic Clinical Lectureship post

British Heart Foundation Clinical Research Training Fellowship

‘SmartHeart’ EPSRC programme

European Union’s Horizon 2020 research and innovation programme

British Heart Foundation

National Institute for Health and Care Research Barts Biomedical Research Centre

Barts Health NHS Trust

Queen Mary University of London

St George’s University Hospitals

NHS Foundation Trust

St George’s University of London

Publisher

Oxford University Press (OUP)

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