Research in diabetes, especially when it comes to building data-driven models to forecast future glucose values, is hindered by the sensitive nature of the data. Because researchers do not share the same data between studies, progress is hard to assess. This paper aims at comparing the most promising algorithms in the field, namely Feedforward Neural Networks (FFNN), Long Short-Term Memory (LSTM) Recurrent Neural Networks, Extreme Learning Machines (ELM), Support Vector Regression (SVR) and Gaussian Processes (GP). They are personalized and trained on a population of 10 virtual children from the Type 1 Diabetes Metabolic Simulator software to predict future glucose values at a prediction horizon of 30 minutes. The performances of the models are evaluated using the Root Mean Squared Error (RMSE) and the Continuous Glucose-Error Grid Analysis (CG-EGA). While most of the models end up having low RMSE, the GP model with a Dot-Product kernel (GP-DP), a novel usage in the context of glucose prediction, has the lowest. Despite having good RMSE values, we show that the models do not necessarily exhibit a good clinical acceptability, measured by the CG-EGA. Only the LSTM, SVR and GP-DP models have overall acceptable results, each of them performing best in one of the glycemia regions.
This paper presents the Derivatives Combination Predictor (DCP), a novel model fusion algorithm for making long-term glucose predictions for diabetic people. First, using the history of glucose predictions made by several models, the future glucose variation at a given horizon is predicted. Then, by accumulating the past predicted variations starting from a known glucose value, the fused glucose prediction is computed. A new loss function is introduced to make the DCP model learn to react faster to changes in glucose variations. The algorithm has been tested on 10 in-silico type-1 diabetic children from the T1DMS software. Three initial predictors have been used: a Gaussian process regressor, a feed-forward neural network and an extreme learning machine model. The DCP and two other fusion algorithms have been evaluated at a prediction horizon of 120 minutes with the root-mean-squared error of the prediction, the root-mean-squared error of the predicted variation, and the continuous glucose-error grid analysis. By making a successful trade-off between prediction accuracy and predicted-variation accuracy, the DCP, alongside with its specifically designed loss function, improves the clinical acceptability of the predictions, and therefore the safety of the model for diabetic people.
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