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Chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models
In patients with type 1 diabetes mellitus (T1DM), glucose dynamics are influenced by insulin reactions, diet, lifestyle, etc., and characterized by instability and nonlinearity. With the objective of a dependable decision support system for T1DM self-management, we aim to model glucose dynamics usin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524948/ https://www.ncbi.nlm.nih.gov/pubmed/28740090 http://dx.doi.org/10.1038/s41598-017-06478-4 |
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author | Frandes, Mirela Timar, Bogdan Timar, Romulus Lungeanu, Diana |
author_facet | Frandes, Mirela Timar, Bogdan Timar, Romulus Lungeanu, Diana |
author_sort | Frandes, Mirela |
collection | PubMed |
description | In patients with type 1 diabetes mellitus (T1DM), glucose dynamics are influenced by insulin reactions, diet, lifestyle, etc., and characterized by instability and nonlinearity. With the objective of a dependable decision support system for T1DM self-management, we aim to model glucose dynamics using their nonlinear chaotic properties. A group of patients was monitored via continuous glucose monitoring (CGM) sensors for several days under free-living conditions. We assessed the glycemic variability (GV) and chaotic properties of each time series. Time series were subsequently transformed into the phase-space and individual autoregressive (AR) models were applied to predict glucose values over 30-minute and 60-minute prediction horizons (PH). The logistic smooth transition AR (LSTAR) model provided the best prediction accuracy for patients with high GV. For a PH of 30 minutes, the average values of root mean squared error (RMSE) and mean absolute error (MAE) for the LSTAR model in the case of patients in the hypoglycemia range were 5.83 ( ± 1.95) mg/dL and 5.18 ( ± 1.64) mg/dL, respectively. For a PH of 60 minutes, the average values of RMSE and MAE were 7.43 ( ± 1.87) mg/dL and 6.54 ( ± 1.6) mg/dL, respectively. Without the burden of measuring exogenous information, nonlinear regime-switching AR models provided fast and accurate results for glucose prediction. |
format | Online Article Text |
id | pubmed-5524948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55249482017-07-26 Chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models Frandes, Mirela Timar, Bogdan Timar, Romulus Lungeanu, Diana Sci Rep Article In patients with type 1 diabetes mellitus (T1DM), glucose dynamics are influenced by insulin reactions, diet, lifestyle, etc., and characterized by instability and nonlinearity. With the objective of a dependable decision support system for T1DM self-management, we aim to model glucose dynamics using their nonlinear chaotic properties. A group of patients was monitored via continuous glucose monitoring (CGM) sensors for several days under free-living conditions. We assessed the glycemic variability (GV) and chaotic properties of each time series. Time series were subsequently transformed into the phase-space and individual autoregressive (AR) models were applied to predict glucose values over 30-minute and 60-minute prediction horizons (PH). The logistic smooth transition AR (LSTAR) model provided the best prediction accuracy for patients with high GV. For a PH of 30 minutes, the average values of root mean squared error (RMSE) and mean absolute error (MAE) for the LSTAR model in the case of patients in the hypoglycemia range were 5.83 ( ± 1.95) mg/dL and 5.18 ( ± 1.64) mg/dL, respectively. For a PH of 60 minutes, the average values of RMSE and MAE were 7.43 ( ± 1.87) mg/dL and 6.54 ( ± 1.6) mg/dL, respectively. Without the burden of measuring exogenous information, nonlinear regime-switching AR models provided fast and accurate results for glucose prediction. Nature Publishing Group UK 2017-07-24 /pmc/articles/PMC5524948/ /pubmed/28740090 http://dx.doi.org/10.1038/s41598-017-06478-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Frandes, Mirela Timar, Bogdan Timar, Romulus Lungeanu, Diana Chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models |
title | Chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models |
title_full | Chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models |
title_fullStr | Chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models |
title_full_unstemmed | Chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models |
title_short | Chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models |
title_sort | chaotic time series prediction for glucose dynamics in type 1 diabetes mellitus using regime-switching models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524948/ https://www.ncbi.nlm.nih.gov/pubmed/28740090 http://dx.doi.org/10.1038/s41598-017-06478-4 |
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