Characterizing the hypertensive cardiovascular phenotype in the UK Biobank

Author:

Elghazaly Hussein1,McCracken Celeste2,Szabo Liliana345ORCID,Malcolmson James4,Manisty Charlotte H46,Davies Alun H1,Piechnik Stefan K2,Harvey Nicholas C78,Neubauer Stefan2ORCID,Mohiddin Saidi A34,Petersen Steffen E34910ORCID,Raisi-Estabragh Zahra34ORCID

Affiliation:

1. Department of Surgery and Cancer, Imperial College London and Imperial College NHS Trust , South Kensington, SW7 2BX London , UK

2. Division of Cardiovascular Medicine, 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

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

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

5. Semmelweis University, Heart and Vascular Center , Budapest Hungary

6. Institute of Cardiovascular Science, University College London , London , UK

7. MRC Lifecourse Epidemiology Centre, University of Southampton , Southampton SO16 6YD , UK

8. NIHR Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton NHS Foundation Trust , Southampton SO16 6YD , UK

9. Health Data Research UK , London , UK

10. Alan Turing Institute , London , UK

Abstract

Abstract Aims To describe hypertension-related cardiovascular magnetic resonance (CMR) phenotypes in the UK Biobank considering variations across patient populations. Methods and results We studied 39 095 (51.5% women, mean age: 63.9 ± 7.7 years, 38.6% hypertensive) participants with CMR data available. Hypertension status was ascertained through health record linkage. Associations between hypertension and CMR metrics were estimated using multivariable linear regression adjusting for major vascular risk factors. Stratified analyses were performed by sex, ethnicity, time since hypertension diagnosis, and blood pressure (BP) control. Results are standardized beta coefficients, 95% confidence intervals, and P-values corrected for multiple testing. Hypertension was associated with concentric left ventricular (LV) hypertrophy (increased LV mass, wall thickness, concentricity index), poorer LV function (lower global function index, worse global longitudinal strain), larger left atrial (LA) volumes, lower LA ejection fraction, and lower aortic distensibility. Hypertension was linked to significantly lower myocardial native T1 and increased LV ejection fraction. Women had greater hypertension-related reduction in aortic compliance than men. The degree of hypertension-related LV hypertrophy was greatest in Black ethnicities. Increasing time since diagnosis of hypertension was linked to adverse remodelling. Hypertension-related remodelling was substantially attenuated in hypertensives with good BP control. Conclusion Hypertension was associated with concentric LV hypertrophy, reduced LV function, dilated poorer functioning LA, and reduced aortic compliance. Whilst the overall pattern of remodelling was consistent across populations, women had greater hypertension-related reduction in aortic compliance and Black ethnicities showed the greatest LV mass increase. Importantly, adverse cardiovascular remodelling was markedly attenuated in hypertensives with good BP control.

Funder

Oxford NIHR Biomedical Research Centre

Oxford British Heart Foundation Centre of Research Excellence

NIHR Biomedical Research Centres

MRC

NIHR Southampton Biomedical Research Centre

Medical Research Council

‘SmartHeart’ EPSRC programme

European Regional Development Fund and Barts Charity

European Union's Horizon 2020 research and innovation programme

British Heart Foundation Clinical Research Training Fellowship

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine

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