Effectiveness and feasibility of cardiovascular disease personalized prevention on high polygenic risk score subjects: a randomized controlled pilot study.

Polygenic risk score coronary artery disease personalized prevention

Journal

European heart journal open
ISSN: 2752-4191
Titre abrégé: Eur Heart J Open
Pays: England
ID NLM: 9918282081406676

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 09 09 2022
revised: 23 11 2022
accepted: 13 12 2022
entrez: 5 1 2023
pubmed: 6 1 2023
medline: 6 1 2023
Statut: epublish

Résumé

The aim of this study was to evaluate the effect of the intervention by proactively sharing a patient's high polygenic risk score (PRS) for coronary artery disease (CAD). Outcomes included: (i) reduction in cardiovascular disease (CVD) risk factors over 12 months; (ii) difference in purchased prescriptions of lipid-lowering and anti-hypertensive drugs between intervention group and control group subjects; and (iii) opinion of the participating physicians and subjects on PRS usefulness. This randomized controlled trial was conducted among middle-aged subjects with a top 20% CAD PRS in a family medicine setting. Participants were selected from 26 953 Estonian Biobank cohort participants. Subjects were informed and counselled about their PRS score and CAD risk using the visual tool at baseline (Visit I), counselling session (Visit II), and on the final Visit III at 12 months. The primary endpoint was not significantly different. However, the intervention group participants had a significantly higher probability of initiating statin treatment compared with the controls. Their levels of LDL-cholesterol (LDL-C) were significantly decreased compared with baseline on Visit III and significantly lower than in the control group. The vast majority of participating family physicians believe that finding out about genetic risks will affect the subject's lifestyle and medication compliance. Most of our outcome measures were in favour of this intervention. Participants achieved larger changes in cholesterol and blood pressure values. The vast majority (98.4%) of family physicians are interested in continuing to use genetic risk assessment in practice.

Identifiants

pubmed: 36600884
doi: 10.1093/ehjopen/oeac079
pii: oeac079
pmc: PMC9803971
doi:

Types de publication

Journal Article

Langues

eng

Pagination

oeac079

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.

Déclaration de conflit d'intérêts

Conflict of interest: None declared.

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Auteurs

Margus Viigimaa (M)

Department of Health Technologies, Tallinn University of Technology, Ehitajate tee 5, 19086 Tallinn, Estonia.
Centre of Cardiology, North Estonia Medical Centre, Sütiste St. 19, 13419 Tallinn, Estonia.

Mikk Jürisson (M)

Institute of Family Medicine and Public Health, University of Tartu, Ravila 19, 50411 Tartu, Estonia.

Heti Pisarev (H)

Institute of Family Medicine and Public Health, University of Tartu, Ravila 19, 50411 Tartu, Estonia.

Ruth Kalda (R)

Institute of Family Medicine and Public Health, University of Tartu, Ravila 19, 50411 Tartu, Estonia.

Helene Alavere (H)

Institute of Genomics, University of Tartu, Riia 23b, 51010 Tartu, Estonia.

Alar Irs (A)

Heart Clinic, Tartu University Hospital, L. Puusepa 8, 50406 Tartu, Estonia.

Aet Saar (A)

Centre of Cardiology, North Estonia Medical Centre, Sütiste St. 19, 13419 Tallinn, Estonia.
Heart Clinic, University of Tartu, L. Puusepa 8, 50406 Tartu, Estonia.

Krista Fischer (K)

Institute of Genomics, University of Tartu, Riia 23b, 51010 Tartu, Estonia.
Institute of Mathematics and Statistics, University of Tartu, Narva mnt 18, 51009 Tartu, Estonia.

Kristi Läll (K)

Institute of Genomics, University of Tartu, Riia 23b, 51010 Tartu, Estonia.

Krista Kruuv-Käo (K)

Institute of Genomics, University of Tartu, Riia 23b, 51010 Tartu, Estonia.

Nina Mars (N)

Institute for Molecular Medicine Finland, University of Helsinki, Tukholmankatu 8, 00014 Helsinki, Finland.

Elisabeth Widen (E)

Institute for Molecular Medicine Finland, University of Helsinki, Tukholmankatu 8, 00014 Helsinki, Finland.

Samuli Ripatti (S)

Institute for Molecular Medicine Finland, University of Helsinki, Tukholmankatu 8, 00014 Helsinki, Finland.

Andres Metspalu (A)

Institute of Genomics, University of Tartu, Riia 23b, 51010 Tartu, Estonia.

Classifications MeSH