Abstract
Coronary artery disease (CAD) is the leading global cause of mortality and has substantial heritability with a polygenic architecture. Recent approaches of risk prediction were based on polygenic risk scores (PRS) not taking possible nonlinear effects into account and restricted in that they focused on genetic loci associated with CAD, only. We benchmarked PRS, (penalized) logistic regression, naïve Bayes (NB), random forests (RF), support vector machines (SVM), and gradient boosting (GB) on a data set of 7,736 CAD cases and 6,774 controls from Germany to identify the algorithms for most accurate classification of CAD status. The final models were tested on an independent data set from Germany (527 CAD cases and 473 controls). We found PRS to be the best algorithm, yielding an area under the receiver operating curve (AUC) of 0.92 (95% CI [0.90, 0.95], 50,633 loci) in the German test data. NB and SVM (AUC ~ 0.81) performed better than RF and GB (AUC ~ 0.75). We conclude that using PRS to predict CAD is superior to machine learning methods.
| Original language | English |
|---|---|
| Journal | Genetic Epidemiology |
| Volume | 44 |
| Issue number | 2 |
| Pages (from-to) | 125-138 |
| Number of pages | 14 |
| ISSN | 0741-0395 |
| DOIs | |
| Publication status | Published - 01.03.2020 |
Funding
I. R. K. was supported by a grant from the Cluster of Excellence Inflammation at Interfaces (funded by the Deutsche Forschungsgemeinschaft), by the Deutsche Forschungsgemeinschaft (grant KO2250/7) and the German Center for Cardiovascular Research (funded by the Bundesministerium für Bildung und Forschung, grant 81Z1700103).
Research Areas and Centers
- Research Area: Medical Genetics