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Blood Glucose Level Time Series Forecasting: Nested Deep Ensemble Learning Lag Fusion
Blood glucose level prediction is a critical aspect of diabetes management. It enables individuals to make informed decisions about their insulin dosing, diet, and physical activity. This, in turn, improves their quality of life and reduces the risk of chronic and acute complications. One conundrum...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135844/ https://www.ncbi.nlm.nih.gov/pubmed/37106674 http://dx.doi.org/10.3390/bioengineering10040487 |
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author | Khadem, Heydar Nemat, Hoda Elliott, Jackie Benaissa, Mohammed |
author_facet | Khadem, Heydar Nemat, Hoda Elliott, Jackie Benaissa, Mohammed |
author_sort | Khadem, Heydar |
collection | PubMed |
description | Blood glucose level prediction is a critical aspect of diabetes management. It enables individuals to make informed decisions about their insulin dosing, diet, and physical activity. This, in turn, improves their quality of life and reduces the risk of chronic and acute complications. One conundrum in developing time-series forecasting models for blood glucose level prediction is to determine an appropriate length for look-back windows. On the one hand, studying short histories foists the risk of information incompletion. On the other hand, analysing long histories might induce information redundancy due to the data shift phenomenon. Additionally, optimal lag lengths are inconsistent across individuals because of the domain shift occurrence. Therefore, in bespoke analysis, either optimal lag values should be found for each individual separately or a globally suboptimal lag value should be used for all. The former approach degenerates the analysis’s congruency and imposes extra perplexity. With the latter, the fine-tunned lag is not necessarily the optimum option for all individuals. To cope with this challenge, this work suggests an interconnected lag fusion framework based on nested meta-learning analysis that improves the accuracy and precision of predictions for personalised blood glucose level forecasting. The proposed framework is leveraged to generate blood glucose prediction models for patients with type 1 diabetes by scrutinising two well-established publicly available Ohio type 1 diabetes datasets. The models developed undergo vigorous evaluation and statistical analysis from mathematical and clinical perspectives. The results achieved underpin the efficacy of the proposed method in blood glucose level time-series prediction analysis. |
format | Online Article Text |
id | pubmed-10135844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101358442023-04-28 Blood Glucose Level Time Series Forecasting: Nested Deep Ensemble Learning Lag Fusion Khadem, Heydar Nemat, Hoda Elliott, Jackie Benaissa, Mohammed Bioengineering (Basel) Article Blood glucose level prediction is a critical aspect of diabetes management. It enables individuals to make informed decisions about their insulin dosing, diet, and physical activity. This, in turn, improves their quality of life and reduces the risk of chronic and acute complications. One conundrum in developing time-series forecasting models for blood glucose level prediction is to determine an appropriate length for look-back windows. On the one hand, studying short histories foists the risk of information incompletion. On the other hand, analysing long histories might induce information redundancy due to the data shift phenomenon. Additionally, optimal lag lengths are inconsistent across individuals because of the domain shift occurrence. Therefore, in bespoke analysis, either optimal lag values should be found for each individual separately or a globally suboptimal lag value should be used for all. The former approach degenerates the analysis’s congruency and imposes extra perplexity. With the latter, the fine-tunned lag is not necessarily the optimum option for all individuals. To cope with this challenge, this work suggests an interconnected lag fusion framework based on nested meta-learning analysis that improves the accuracy and precision of predictions for personalised blood glucose level forecasting. The proposed framework is leveraged to generate blood glucose prediction models for patients with type 1 diabetes by scrutinising two well-established publicly available Ohio type 1 diabetes datasets. The models developed undergo vigorous evaluation and statistical analysis from mathematical and clinical perspectives. The results achieved underpin the efficacy of the proposed method in blood glucose level time-series prediction analysis. MDPI 2023-04-19 /pmc/articles/PMC10135844/ /pubmed/37106674 http://dx.doi.org/10.3390/bioengineering10040487 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Khadem, Heydar Nemat, Hoda Elliott, Jackie Benaissa, Mohammed Blood Glucose Level Time Series Forecasting: Nested Deep Ensemble Learning Lag Fusion |
title | Blood Glucose Level Time Series Forecasting: Nested Deep Ensemble Learning Lag Fusion |
title_full | Blood Glucose Level Time Series Forecasting: Nested Deep Ensemble Learning Lag Fusion |
title_fullStr | Blood Glucose Level Time Series Forecasting: Nested Deep Ensemble Learning Lag Fusion |
title_full_unstemmed | Blood Glucose Level Time Series Forecasting: Nested Deep Ensemble Learning Lag Fusion |
title_short | Blood Glucose Level Time Series Forecasting: Nested Deep Ensemble Learning Lag Fusion |
title_sort | blood glucose level time series forecasting: nested deep ensemble learning lag fusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135844/ https://www.ncbi.nlm.nih.gov/pubmed/37106674 http://dx.doi.org/10.3390/bioengineering10040487 |
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