This study presents a Deep Learning framework for forecasting blood glucose levels at a time horizon of 45 and 60 min using ElectroCardioGraphy (ECG)–derived features alongside baseline glucose readings. Using data from the D1NAMO dataset, we extracted and normalized Heart Rate (HR) and Heart Rate Variability (HRV) metrics and categorized future glucose levels into clinically meaningful bins. A feedforward neural network was trained to classify these categories. The resulting model demonstrated promising classification performance on both prediction horizons, with balanced predictive capability across most glucose categories. To enhance transparency and clinical relevance, we employed SHapley Additive exPlanations (SHAP) to assess feature importance and interpret the model’s predictions. SHAP analysis revealed that HR and HRV metrics—particularly hr_max, hr_min, hr_std, and nni_mean—provide valuable complementary information to current glucose levels for predicting short-term glycemic trends. This highlights the potential of ECG–derived features as predictive biomarkers for short-term glycemic changes. Overall, the proposed framework offers a promising and explainable approach to glucose forecasting, supporting transparency, physiological insight, and trust–key factors for the adoption of predictive models in real-time clinical monitoring. © The Author(s), under exclusive license to Springer Nature Switzerland AG 2026.

Personalized Multi-Horizon Glucose Forecasting in Type 1 Diabetes via Deep Learning / Santopaolo, A., Basile, I., Giuseppi, A., Sannino, G.. - 2806:(2026), pp. 161-170. (20th International Conference on Soft Computing Models in Industrial and Environmental Applications, SOCO 2025 Salamanca; Spain ) [10.1007/978-3-032-19763-4_15].

Personalized Multi-Horizon Glucose Forecasting in Type 1 Diabetes via Deep Learning

Alessandro Santopaolo
;
Alessandro Giuseppi;
2026

Abstract

This study presents a Deep Learning framework for forecasting blood glucose levels at a time horizon of 45 and 60 min using ElectroCardioGraphy (ECG)–derived features alongside baseline glucose readings. Using data from the D1NAMO dataset, we extracted and normalized Heart Rate (HR) and Heart Rate Variability (HRV) metrics and categorized future glucose levels into clinically meaningful bins. A feedforward neural network was trained to classify these categories. The resulting model demonstrated promising classification performance on both prediction horizons, with balanced predictive capability across most glucose categories. To enhance transparency and clinical relevance, we employed SHapley Additive exPlanations (SHAP) to assess feature importance and interpret the model’s predictions. SHAP analysis revealed that HR and HRV metrics—particularly hr_max, hr_min, hr_std, and nni_mean—provide valuable complementary information to current glucose levels for predicting short-term glycemic trends. This highlights the potential of ECG–derived features as predictive biomarkers for short-term glycemic changes. Overall, the proposed framework offers a promising and explainable approach to glucose forecasting, supporting transparency, physiological insight, and trust–key factors for the adoption of predictive models in real-time clinical monitoring. © The Author(s), under exclusive license to Springer Nature Switzerland AG 2026.
2026
20th International Conference on Soft Computing Models in Industrial and Environmental Applications, SOCO 2025
blood glucose levels forecasting; heart rate variability; type 1 diabetes; deep learning; explainable ai
04 Pubblicazione in atti di convegno::04b Atto di convegno in volume
Personalized Multi-Horizon Glucose Forecasting in Type 1 Diabetes via Deep Learning / Santopaolo, A., Basile, I., Giuseppi, A., Sannino, G.. - 2806:(2026), pp. 161-170. (20th International Conference on Soft Computing Models in Industrial and Environmental Applications, SOCO 2025 Salamanca; Spain ) [10.1007/978-3-032-19763-4_15].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1754404
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