Tayside Screening For Cardiac Events (TASCFORCE) study: a prospective cardiovascular risk screening study.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
21 10 2022
Historique:
entrez: 21 10 2022
pubmed: 22 10 2022
medline: 26 10 2022
Statut: epublish

Résumé

Risk factor-based models struggle to accurately predict the development of cardiovascular disease (CVD) at the level of the individual. Ways of identifying people with low predicted risk who will develop CVD would allow stratified advice and support informed treatment decisions about the initiation or adjustment of preventive medication, and this is the aim of this prospective cohort study. The Tayside Screening for Cardiac Events (TASCFORCE) study recruited men and women aged≥40 years, free from known CVD, with a predicted 10-year risk of coronary heart disease<20%. If B-type natriuretic peptide (BNP) was greater than their gender median, participants were offered a whole-body contrast-enhanced MRI (WBCE-MRI) scan (cardiac imaging, whole-body angiography to determine left ventricular parameters, delayed gadolinium enhancement, atheroma burden). Blood, including DNA, was stored for future biomarker assays. Participants are being followed up using electronic record-linkage cardiovascular outcomes. 4423 (1740, 39.3% men) were recruited. Mean age was 52.3 years with a median BNP of 7.50 ng/L and 15.30 ng/L for men and women, respectively. 602 had a predicted 10-year risk of 10%-19.9%, with the remainder<10%. Age, female sex, ex-smoking status, lower heart rate, higher high-density lipoprotein and lower total cholesterol were independently associated with higher log10 BNP levels. Mean left ventricular mass was 129.2 g and 87.0 g in men and women, respectively. The TASCFORCE study is investigating the ability of a screening programme, using BNP and WBCE-MRI, at the time of enrolment, to evaluate prediction of CVD in a population at low/intermediate risk. Blood stored for future biomarker analyses will allow testing/development of novel biomarkers. We believe this could be a new UK Framingham study allowing study for many years to come. ISRCTN38976321.

Identifiants

pubmed: 36270757
pii: bmjopen-2022-063594
doi: 10.1136/bmjopen-2022-063594
pmc: PMC9594527
doi:

Substances chimiques

Natriuretic Peptide, Brain 114471-18-0
Gadolinium AU0V1LM3JT
Contrast Media 0
Biomarkers 0
Cholesterol 97C5T2UQ7J
Lipoproteins, HDL 0

Banques de données

ISRCTN
['ISRCTN38976321']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e063594

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Matthew A Lambert (MA)

Stroke, NHS Tayside, Dundee, UK.

J Graeme Houston (JG)

Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.

Roberta Littleford (R)

Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.

Catherine A Fitton (CA)

Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.

Allan Struthers (A)

Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.

Frank Sullivan (F)

School of Medicine, University of St Andrews, St Andrews, UK.
North York General Hospital, Toronto, Ontario, Canada.

Stephen Gandy (S)

Medical Physics, NHS Tayside, Dundee, UK.

Jill J F Belch (JJF)

Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK j.j.f.belch@dundee.ac.uk.

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Classifications MeSH