Improved cardiovascular risk prediction using targeted plasma proteomics in primary prevention

Author:

Hoogeveen Renate M1ORCID,Pereira João P Belo1,Nurmohamed Nick S12ORCID,Zampoleri Veronica3,Bom Michiel J2,Baragetti Andrea3ORCID,Boekholdt S Matthijs4,Knaapen Paul2,Khaw Kay-Tee5ORCID,Wareham Nicholas J6ORCID,Groen Albert K1,Catapano Alberico L37ORCID,Koenig Wolfgang8910,Levin Evgeni111,Stroes Erik S G1ORCID

Affiliation:

1. Department of Vascular Medicine, Amsterdam University Medical Centers, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands

2. Department of Cardiology, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands

3. Department of Pharmacological and Biomolecular Sciences, University of Milan, Via Balzaretti 9, 20133 Milan, Italy

4. Department of Cardiology, Amsterdam University Medical Centers, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands

5. Department of Public Health and Primary Care, University of Cambridge, 2 Worts' Causeway, Cambridge, UK

6. Medical Research Council Epidemiology Unit, University of Cambridge, Cambridge CB2 0QQ, UK

7. Multimedica IRCCS, Milano, Italy

8. Klinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany

9. DZHK (German Centre for Cardiovascular Research), Partner site Munich Heart Alliance, Munich, Germany

10. Institute of Epidemiology and Medical Biometry, Ulm University, Ulm, Germany

11. HorAIzon BV, Delft, the Netherlands

Abstract

Abstract Aims In the era of personalized medicine, it is of utmost importance to be able to identify subjects at the highest cardiovascular (CV) risk. To date, single biomarkers have failed to markedly improve the estimation of CV risk. Using novel technology, simultaneous assessment of large numbers of biomarkers may hold promise to improve prediction. In the present study, we compared a protein-based risk model with a model using traditional risk factors in predicting CV events in the primary prevention setting of the European Prospective Investigation (EPIC)-Norfolk study, followed by validation in the Progressione della Lesione Intimale Carotidea (PLIC) cohort. Methods and results Using the proximity extension assay, 368 proteins were measured in a nested case–control sample of 822 individuals from the EPIC-Norfolk prospective cohort study and 702 individuals from the PLIC cohort. Using tree-based ensemble and boosting methods, we constructed a protein-based prediction model, an optimized clinical risk model, and a model combining both. In the derivation cohort (EPIC-Norfolk), we defined a panel of 50 proteins, which outperformed the clinical risk model in the prediction of myocardial infarction [area under the curve (AUC) 0.754 vs. 0.730; P < 0.001] during a median follow-up of 20 years. The clinically more relevant prediction of events occurring within 3 years showed an AUC of 0.732 using the clinical risk model and an AUC of 0.803 for the protein model (P < 0.001). The predictive value of the protein panel was confirmed to be superior to the clinical risk model in the validation cohort (AUC 0.705 vs. 0.609; P < 0.001). Conclusion In a primary prevention setting, a proteome-based model outperforms a model comprising clinical risk factors in predicting the risk of CV events. Validation in a large prospective primary prevention cohort is required to address the value for future clinical implementation in CV prevention.

Funder

European Research Area Network on Cardiovascular Diseases

European Union’s Horizon 2020

Cancer Research UK

Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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