A physical activity-intensity driven glycemic model for type 1 diabetes. (November 2022)
- Record Type:
- Journal Article
- Title:
- A physical activity-intensity driven glycemic model for type 1 diabetes. (November 2022)
- Main Title:
- A physical activity-intensity driven glycemic model for type 1 diabetes
- Authors:
- Hobbs, Nicole
Samadi, Sediqeh
Rashid, Mudassir
Shahidehpour, Andrew
Askari, Mohammad Reza
Park, Minsun
Quinn, Laurie
Cinar, Ali - Abstract:
- Highlights: Factors that affect the glycemic response include the intensity and duration of physical activity, plasma insulin concentrations, and the individual physical fitness level. To model the glycemic response for a person with type 1 diabetes to physical activity, these factors must be considered. Several physiological models describing the glycemic response to physical activity are proposed by incorporating various model terms. A model with terms accommodating endogenous glucose production, glucose transfer, and insulin-independent glucose utilization enable an improved estimation of glycemic responses to physical activity. Abstract: Background and Objective: The glucose response to physical activity for a person with type 1 diabetes (T1D) depends upon the intensity and duration of the physical activity, plasma insulin concentrations, and the individual physical fitness level. To accurately model the glycemic response to physical activity, these factors must be considered. Methods: Several physiological models describing the glycemic response to physical activity are proposed by incorporating model terms proportional to the physical activity intensity and duration describing endogenous glucose production (EGP), glucose utilization, and glucose transfer from the plasma to tissues. Leveraging clinical data of T1D during physical activity, each model fit is assessed. Results: The proposed model with terms accommodating EGP, glucose transfer, and insulin-independentHighlights: Factors that affect the glycemic response include the intensity and duration of physical activity, plasma insulin concentrations, and the individual physical fitness level. To model the glycemic response for a person with type 1 diabetes to physical activity, these factors must be considered. Several physiological models describing the glycemic response to physical activity are proposed by incorporating various model terms. A model with terms accommodating endogenous glucose production, glucose transfer, and insulin-independent glucose utilization enable an improved estimation of glycemic responses to physical activity. Abstract: Background and Objective: The glucose response to physical activity for a person with type 1 diabetes (T1D) depends upon the intensity and duration of the physical activity, plasma insulin concentrations, and the individual physical fitness level. To accurately model the glycemic response to physical activity, these factors must be considered. Methods: Several physiological models describing the glycemic response to physical activity are proposed by incorporating model terms proportional to the physical activity intensity and duration describing endogenous glucose production (EGP), glucose utilization, and glucose transfer from the plasma to tissues. Leveraging clinical data of T1D during physical activity, each model fit is assessed. Results: The proposed model with terms accommodating EGP, glucose transfer, and insulin-independent glucose utilization allow for an improved simulation of physical activity glycemic responses with the greatest reduction in model error (mean absolute percentage error: 16.11 ± 4.82 vs. 19.49 ± 5.87, p = 0.002). Conclusions: The development of a physiologically plausible model with model terms representing each major contributor to glucose metabolism during physical activity can outperform traditional models with physical activity described through glucose utilization alone. This model accurately describes the relation of plasma insulin and physical activity intensity on glucose production and glucose utilization to generate the appropriately increasing, decreasing or stable glucose response for each physical activity condition. The proposed model will enable the in silico evaluation of automated insulin dosing algorithms designed to mitigate the effects of physical activity with the appropriate relationship between the reduction in basal insulin and the corresponding glycemic excursion. … (more)
- Is Part Of:
- Computer methods and programs in biomedicine. Volume 226(2022)
- Journal:
- Computer methods and programs in biomedicine
- Issue:
- Volume 226(2022)
- Issue Display:
- Volume 226, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 226
- Issue:
- 2022
- Issue Sort Value:
- 2022-0226-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-11
- Subjects:
- Physical activity -- Type 1 diabetes -- Physiological modeling
T1D Type 1 Diabetes -- BGC blood glucose concentration -- CGM continuous glucose monitor -- k12 transfer rate between accessible and inaccessible compartments -- ke insulin elimination rate from plasma -- VI insulin distribution volume -- VG glucose distribution volume -- EGP0 endogenous glucose concentration extrapolated to zero insulin concentration -- F01 insulin-independent glucose flux -- tmax, I time to maximum absorption of insulin -- tmax, G time to maximum absorption of oral carbohydrates -- tsc time constant for diffusion between plasma and subcutaneous glucose
Medicine -- Computer programs -- Periodicals
Biology -- Computer programs -- Periodicals
Computers -- Periodicals
Medicine -- Periodicals
Médecine -- Logiciels -- Périodiques
Biologie -- Logiciels -- Périodiques
Biology -- Computer programs
Medicine -- Computer programs
Periodicals
Electronic journals
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01692607 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cmpb.2022.107153 ↗
- Languages:
- English
- ISSNs:
- 0169-2607
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3394.095000
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