Abstract
AbstractUnderstanding how risk factors interact to jointly influence disease risk can provide insights into disease development and improve risk prediction. We introducesurvivalFM, a machine learning extension to the widely used Cox proportional hazards model that incorporates estimation of all potential pairwise interaction effects on time-to-event outcomes. The method relies on learning a low-rank factorized approximation of the interaction effects, hence overcoming the computational and statistical limitations of fitting these terms in models involving many predictor variables. The resulting model is fully interpretable, providing access to the estimates of both individual effects and the approximated interactions. Comprehensive evaluation ofsurvivalFMusing the UK Biobank dataset across ten disease examples and a variety of clinical risk factors and omics data modalities shows improved discrimination and reclassification performance (65% and 97.5% of the scenarios tested, respectively). Considering a clinical scenario of cardiovascular risk prediction using predictors from the established QRISK3 model, we further show that the comprehensive interaction modelling adds predictive value beyond the individual and age interaction effects currently included. These results demonstrate that comprehensive modelling of interactions can facilitate advanced insights into disease development and improve risk predictions.
Publisher
Cold Spring Harbor Laboratory