Incident cardiovascular events and imaging phenotypes in UK Biobank participants with past cancer

Author:

Raisi-Estabragh ZahraORCID,Cooper Jackie,McCracken Celeste,Crosbie Emma J,Walter Fiona M,Manisty Charlotte H,Robson John,Mamas Mamas AORCID,Harvey Nicholas C,Neubauer Stefan,Petersen Steffen EORCID

Abstract

ObjectivesTo evaluate incident cardiovascular outcomes and imaging phenotypes in UK Biobank participants with previous cancer.MethodsCancer and cardiovascular disease (CVD) diagnoses were ascertained using health record linkage. Participants with cancer history (breast, lung, prostate, colorectal, uterus, haematological) were propensity matched on vascular risk factors to non-cancer controls. Competing risk regression was used to calculate subdistribution HRs (SHRs) for associations of cancer history with incident CVD (ischaemic heart disease (IHD), non-ischaemic cardiomyopathy (NICM), heart failure (HF), atrial fibrillation/flutter, stroke, pericarditis, venous thromboembolism (VTE)) and mortality outcomes (any CVD, IHD, HF/NICM, stroke, hypertensive disease) over 11.8±1.7 years of prospective follow-up. Linear regression was used to assess associations of cancer history with left ventricular (LV) and left atrial metrics.ResultsWe studied 18 714 participants (67% women, age: 62 (IQR: 57–66) years, 97% white ethnicities) with cancer history, including 1354 individuals with cardiovascular magnetic resonance. Participants with cancer had high burden of vascular risk factors and prevalent CVDs. Haematological cancer was associated with increased risk of all incident CVDs considered (SHRs: 1.92–3.56), larger chamber volumes, lower ejection fractions, and poorer LV strain. Breast cancer was associated with increased risk of selected CVDs (NICM, HF, pericarditis and VTE; SHRs: 1.34–2.03), HF/NICM death, hypertensive disease death, lower LV ejection fraction, and lower LV global function index. Lung cancer was associated with increased risk of pericarditis, HF, and CVD death. Prostate cancer was linked to increased VTE risk.ConclusionsCancer history is linked to increased risk of incident CVDs and adverse cardiac remodelling independent of shared vascular risk factors.

Funder

Engineering and Physical Sciences Research Council

Medical Research Council

British Heart Foundation

Horizon 2020 Framework Programme

National Institute for Health and Care Research

NIHR Manchester Biomedical Research Centre

Cancer Research UK

Barts Charity

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

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