Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status

Damian Gola, Jeannette Erdmann, Bertram Müller-Myhsok, Heribert Schunkert, Inke R. König*

*Corresponding author for this work
3 Citations (Scopus)

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 languageEnglish
JournalGenetic Epidemiology
Volume44
Issue number2
Pages (from-to)125-138
Number of pages14
ISSN0741-0395
DOIs
Publication statusPublished - 01.03.2020

Research Areas and Centers

  • Research Area: Medical Genetics

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