Affiliation:
1. Department of Biochemistry, Medical College of Wisconsin , Milwaukee, Wisconsin, USA
2. Department of Computational Biomedicine, Cedars-Sinai , Beverly Hills, California, USA
Abstract
AbstractObjectiveThe rate of diabetic complication progression varies across individuals and understanding factors that alter the rate of complication progression may uncover new clinical interventions for personalized diabetes management.Materials and MethodsWe explore how various machine learning (ML) models and types of electronic health records (EHRs) can predict fast versus slow onset of neuropathy, nephropathy, ocular disease, or cardiovascular disease using only patient data collected prior to diabetes diagnosis.ResultsWe find that optimized random forest models performed best to accurately predict the diagnosis of a diabetic complication, with the most effective model distinguishing between fast versus slow nephropathy (AUROC = 0.75). Using all data sets combined allowed for the highest model predictive performance, and social history or laboratory alone were most predictive. SHapley Additive exPlanations (SHAP) model interpretation allowed for exploration of predictors of fast and slow complication diagnosis, including underlying biases present in the EHR. Patients in the fast group had more medical visits, incurring a potential informed decision bias.DiscussionOur study is unique in the realm of ML studies as it leverages SHAP as a starting point to explore patient markers not routinely used in diabetes monitoring. A mix of both bias and biological processes is likely present in influencing a model’s ability to distinguish between groups.ConclusionOverall, model interpretation is a critical step in evaluating validity of a user-intended endpoint for a model when using EHR data, and predictors affected by bias and those driven by biologic processes should be equally recognized.
Funder
Medical College of Wisconsin
National Center for Research Resources
National Center for Advancing Translational Sciences
National Institutes of Health
Publisher
Oxford University Press (OUP)
Cited by
7 articles.
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