Penalty weighted glucose prediction models could lead to better clinically usage
| Autor: | Ole K. Hejlesen, Morten Hasselstrøm Jensen, Thomas Kronborg, Simon Lebech Cichosz |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
Blood Glucose
Accuracy and precision Computer science Extrapolation Health Informatics Machine learning computer.software_genre Ensemble learning Humans Lead (electronics) Continuous glucose monitoring Artificial neural network CGM business.industry Blood Glucose Self-Monitoring Neural network Computer Science Applications Weighting Type 1 diabetes Diabetes Mellitus Type 1 Glucose Artificial intelligence Neural Networks Computer Prediction business computer Lead time Predictive modelling |
| Zdroj: | Cichosz, S L, Kronborg, T, Jensen, M H & Hejlesen, O 2021, ' Penalty Weighted Glucose Prediction Models Could Lead to Better Clinically Usage ', Computers in Biology and Medicine, vol. 138, 104865 . https://doi.org/10.1016/j.compbiomed.2021.104865 |
| ISSN: | 1879-0534 |
| Popis: | Background and objective Numerous attempts to predict glucose value from continuous glucose monitors (CGM) have been published. However, there is a lack of proper analysis and modeling of penalty for errors in different glycemic ranges. The aim of this study was to investigate the potential for developing glucose prediction models with focus on the clinical aspects. Methods We developed and compared six different models to test which approach were best suited for predicting glucose levels at different lead times between 10 and 60 min. The models were: last observation carried forward, linear extrapolation, ensemble methods using LSBoost and bagging, neural networks, one without error-weights and one with error-weights. The modeling and test were based on 225 type 1 diabetes patients with 315,000 h of CGM data. Results Results show that it is possible to predict glucose levels based on CGM with a reasonable accuracy and precision with a 30-min prediction lead time. A comparison of different methods shows that there are improvements on performance gained from using more advanced machine learning algorithms (MARD 10.26–10.79 @ 30-min lead time) compared to a simple modeling (MARD 10.75–12.97 @ 30-min lead time). Moreover, the proposed use of error weights could lead to better clinical performance of these models, which is an important factor for real usage. E.g., the percentages in the C-zone of the consensus error grid without error-weights (0.57-0.68%) vs including error-weights (0.28%). Conclusions The results point toward that using error weighting in the training of the models could lead to better clinical performance. |
| Databáze: | OpenAIRE |
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