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Journal article

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

Abstract:
Objectives: To evaluate incident cardiovascular outcomes and imaging phenotypes in UK Biobank participants with previous cancer. Methods: Cancer 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. Results: We 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. Conclusions: Cancer history is linked to increased risk of incident CVDs and adverse cardiac remodelling independent of shared vascular risk factors
Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0002-7757-5465
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Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Strategic
Role:
Author
ORCID:
0000-0003-1285-2393
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Role:
Author
ORCID:
0000-0003-0284-8630
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Role:
Author
ORCID:
0000-0002-7191-6476


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Funder identifier:
10.13039/100015652
Grant:
G-002346
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Funder identifier:
10.13039/501100000289
Grant:
CC8640/A23385
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Funder identifier:
10.13039/100014653
Grant:
IS-BRC-1215-20007
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Funder identifier:
10.13039/501100000272
Grant:
NIHR300650
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Funder identifier:
10.13039/501100000274
Grant:
Clinical Research Training Fellowship


Publisher:
BMJ Publishing Group
Journal:
Heart More from this journal
Volume:
109
Issue:
13
Pages:
1007-1015
Publication date:
2023-04-18
Acceptance date:
2022-12-28
DOI:
EISSN:
1468-201X
ISSN:
1355-6037


Language:
English
Keywords:
Pubs id:
1339940
Local pid:
pubs:1339940
Source identifiers:
W4366334417
Deposit date:
2026-05-07
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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