ProtectHearts

Proteomics for Heart Disease Prediction

About ProtectHearts

Cardiovascular disease (CVD) remains the leading cause of death globally for men and women. State-of-the art clinical risk prediction models for CVD use conventional risk factors and polygenic scores (PGS)—a measure of an individuals’ inherited CVD risk. However, the accuracy of current models is moderate and worse in women than men. Protein markers of CVD represent an individual’s current health state and both inherited and environmental disease risk. Indeed, there is evidence that combining conventional risk factors, PGS, and protein markers of CVD may facilitate vast improvements in CVD risk prediction. Furthermore, by modelling inflammation- specific protein markers missing from sex-specific CVD risk models, ProtectHearts will specifically capture excess risk in women.

ProtectHearts will use the world’s largest population-biobank-linked proteomics datasets to 1) develop a novel protein-based risk score (ProtRS); 2) develop an inflammation-specific ProtRS (i-ProtRS); and 3) estimate the clinical utility of these scores when modelled with clinical risk scores and PGS. Cutting-edge machine learning algorithms will be used to establish target proteins for CVD prediction in 100,000 individuals across four European biobanks.

ProtectHearts brings together a physician-scientist Supervisor with proteomics expertise and a Fellow with experience modelling CVD risk prediction using PGS in biobanks. Through a secondment and non-academic placement, the Fellow will gain intersectoral experience. Activities of the training and dissemination work packages will build her competencies in machine learning, advanced statistics and science communication. ProtectHearts will engage clinicians in exploitation of the new sex-specific, comprehensive CVD risk prediction model.

ProtectHearts has the potential to move CVD risk prediction beyond state-of-the-art by improving risk prediction accuracy, specifically in women, using protein-based markers for CVD and CVD-related inflammation.