A gradient boosting machine model improved 5-year ASCVD risk prediction across a diverse cohort including PCE-ineligible patients (AUC 0.835) compared to the pooled cohort equations (AUC 0.775).
Cohort (n=262,923)
Do machine learning models improve 5-year ASCVD risk prediction compared to the Pooled Cohort Equations in a multi-ethnic population?
Machine learning models, particularly Gradient Boosting Machines, improve 5-year ASCVD risk prediction compared to standard Pooled Cohort Equations and can be applied to a broader group of patients, including those ineligible for PCE.
Absolute Event Rate: 0.835% vs 0.775%
lasso penalty, random forest, gradient boosting machine (GBM), extreme gradient boosting] and determined 5-year ASCVD risk prediction, including with and without incorporation of additional EHR variables, and in Asian and Hispanic subgroups. A total of 4309 patients had ASCVD events, with 2077 in PCE-ineligible patients. GBM performance in the full cohort, including PCE-ineligible patients (area under receiver-operating characteristic curve (AUC) 0.835, 95% confidence interval (CI): 0.825-0.846), was significantly better than that of the PCE in the PCE-eligible cohort (AUC 0.775, 95% CI: 0.755-0.794). Among patients aged 40-79, GBM performed similarly before (AUC 0.784, 95% CI: 0.759-0.808) and after (AUC 0.790, 95% CI: 0.765-0.814) incorporating additional EHR data. Overall, ML models achieved comparable or improved performance compared to the PCE while allowing risk discrimination in a larger group of patients including PCE-ineligible patients. EHR-trained ML models may help bridge important gaps in ASCVD risk prediction.
Ward et al. (Wed,) conducted a cohort in Atherosclerotic cardiovascular disease (n=262,923). Machine learning models (Gradient Boosting Machine) vs. Pooled cohort equations (PCE) was evaluated on 5-year ASCVD risk prediction (Area Under the ROC Curve) (95% CI 0.825-0.846). A gradient boosting machine model improved 5-year ASCVD risk prediction across a diverse cohort including PCE-ineligible patients (AUC 0.835) compared to the pooled cohort equations (AUC 0.775).