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Incorporating a polygenic risk score-triaged coronary calcium score into cardiovascular disease examinations to identify subclinical coronary artery disease (ESCALATE): Protocol for a prospective, nonrandomized implementation trial.

Authors :
Gray, Michael P.
Berman, Yemima
Bottà, Giordano
Grieve, Stuart M.
Ho, Amy
Hu, Jessica
Hyun, Karice
Ingles, Jodie
Jennings, Garry
Kilov, Gary
Levesque, Jean-Frederic
Meikle, Peter
Redfern, Julie
Usherwood, Tim
Vernon, Stephen T.
Nicholls, Stephen J.
Figtree, Gemma A.
Source :
American Heart Journal; Oct2023, Vol. 264, p163-173, 11p
Publication Year :
2023

Abstract

Identifying and targeting established modifiable risk factors has been a successful strategy for reducing the burden of coronary artery disease (CAD) at the population-level. However, up to 1-in-4 patients who present with ST elevation myocardial infarction do so in the absence of such risk factors. Polygenic risk scores (PRS) have demonstrated an ability to improve risk prediction models independent of traditional risk factors and self-reported family history, but a pathway for implementation has yet to be clearly identified. The aim of this study is to examine the utility of a CAD PRS to identify individuals with subclinical CAD via a novel clinical pathway, triaging low or intermediate absolute risk individuals for noninvasive coronary imaging, and examining the impact on shared treatment decisions and participant experience. The ESCALATE study is a 12-month, prospective, multicenter implementation study incorporating PRS into otherwise standard primary care CVD risk assessments, to identify patients at increased lifetime CAD risk for noninvasive coronary imaging. One-thousand eligible participants aged 45 to 65 years old will enter the study, which applies PRS to those considered low or moderate 5-year absolute CVD risk and triages those with CAD PRS ≥80% for a coronary calcium scan. The primary outcome will be the identification of subclinical CAD, defined as a coronary artery calcium score (CACS) >0 Agatston units (AU). Multiple secondary outcomes will be assessed, including baseline CACS ≥100 AU or ≥75th age-/sex-matched percentile, the use and intensity of lipid- and blood pressure-lowering therapeutics, cholesterol and blood pressure levels, and health-related quality of life (HRQOL). This novel trial will generate evidence on the ability of a PRS-triaged CACS to identify subclinical CAD, as well as subsequent differences in traditional risk factor medical management, pharmacotherapy utilization, and participant experience. Australian New Zealand Clinical Trials Registry, ACTRN12622000436774. Trial was prospectively registered on March 18, 2022. https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=383134 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00028703
Volume :
264
Database :
Supplemental Index
Journal :
American Heart Journal
Publication Type :
Academic Journal
Accession number :
171919903
Full Text :
https://doi.org/10.1016/j.ahj.2023.06.009