TY - JOUR
T1 - Modeling continuous glucose monitoring with fractional differential equations subject to shocks
AU - De Gaetano, Anna Maria
AU - Sakulrang, Sasikarn
AU - Borri, Alessandro
AU - Pitocco, Dario
AU - Sungnul, Surattana
AU - Moore, Elvin J.
PY - 2021
Y1 - 2021
N2 - Continuous Glucose Monitoring (CGM) produces long time-series of noisy observations of a single variable (tissue glucose concentration), whose evolution may be explained by a dynamical model. In order to represent the unknown mixture of possible control mechanisms of different orders affecting the measured variable, a fractional differential approach seems justified. In any case, variations in food intake and/or physical activity ought to be taken into account if a plausible interpretation of the dynamics is to be obtained. In the present work, the mathematical construction and the numerical implementation of a Fractional Differential Equations (FDE) initial value problem are systematically reviewed, with the intent of offering the reader a concise and mathematically rigorous description of this approach. An FDE model for CGM is formulated: the model includes compartments for stomach and intestinal glucose contents and for blood and tissue (subcutaneous) glucose concentrations, as well as the shock effects of food ingestion and of increased glucose consumption due to physical activity. The model parameters, including the (non-integer) order of differentiation, are estimated from CGM observations on six Type 1 diabetic patients. The best-fit fractional orders for the six subjects range from 1.59 to 2.13. For comparison, best fits have also been computed for all subjects using an average fractional order of 1.9 and integer orders of 1 and 2.The results indicate that in the case of CGM the fractional differential model, which should be physiologically more appropriate, in fact fits the data much better than the first-order model and also better than the 2nd-order model. (C) 2021 Elsevier Ltd. All rights reserved.
AB - Continuous Glucose Monitoring (CGM) produces long time-series of noisy observations of a single variable (tissue glucose concentration), whose evolution may be explained by a dynamical model. In order to represent the unknown mixture of possible control mechanisms of different orders affecting the measured variable, a fractional differential approach seems justified. In any case, variations in food intake and/or physical activity ought to be taken into account if a plausible interpretation of the dynamics is to be obtained. In the present work, the mathematical construction and the numerical implementation of a Fractional Differential Equations (FDE) initial value problem are systematically reviewed, with the intent of offering the reader a concise and mathematically rigorous description of this approach. An FDE model for CGM is formulated: the model includes compartments for stomach and intestinal glucose contents and for blood and tissue (subcutaneous) glucose concentrations, as well as the shock effects of food ingestion and of increased glucose consumption due to physical activity. The model parameters, including the (non-integer) order of differentiation, are estimated from CGM observations on six Type 1 diabetic patients. The best-fit fractional orders for the six subjects range from 1.59 to 2.13. For comparison, best fits have also been computed for all subjects using an average fractional order of 1.9 and integer orders of 1 and 2.The results indicate that in the case of CGM the fractional differential model, which should be physiologically more appropriate, in fact fits the data much better than the first-order model and also better than the 2nd-order model. (C) 2021 Elsevier Ltd. All rights reserved.
KW - Continuous glucose monitoring
KW - Diabetes
KW - Fractional differential equations
KW - Glucose metabolism
KW - Continuous glucose monitoring
KW - Diabetes
KW - Fractional differential equations
KW - Glucose metabolism
UR - http://hdl.handle.net/10807/221571
U2 - 10.1016/j.jtbi.2021.110776
DO - 10.1016/j.jtbi.2021.110776
M3 - Article
SN - 0022-5193
VL - 526
SP - 110776
EP - 110789
JO - Journal of Theoretical Biology
JF - Journal of Theoretical Biology
ER -