Modeling continuous glucose monitoring with fractional differential equations subject to shocks.

Continuous glucose monitoring Diabetes Fractional differential equations Glucose metabolism

Journal

Journal of theoretical biology
ISSN: 1095-8541
Titre abrégé: J Theor Biol
Pays: England
ID NLM: 0376342

Informations de publication

Date de publication:
07 10 2021
Historique:
received: 12 02 2021
revised: 29 04 2021
accepted: 24 05 2021
pubmed: 1 6 2021
medline: 7 8 2021
entrez: 31 5 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 34058226
pii: S0022-5193(21)00198-3
doi: 10.1016/j.jtbi.2021.110776
pii:
doi:

Substances chimiques

Blood Glucose 0
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

110776

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Andrea De Gaetano (A)

CNR-IRIB, Institute for Biomedical Research and Innovation, National Research Council of Italy, Palermo, Italy; CNR-IASI Biomathematics Laboratory, National Research Council of Italy, Rome, Italy.

Sasikarn Sakulrang (S)

Department of Mathematics, King Mongkut's University of Technology North Bangkok, Thailand; Centre of Excellence in Mathematics, Bangkok, Thailand.

Alessandro Borri (A)

CNR-IASI Biomathematics Laboratory, National Research Council of Italy, Rome, Italy. Electronic address: alessandro.borri@biomatematica.it.

Dario Pitocco (D)

Diabetes Care Unit, Catholic University Faculty of Medicine, Rome, Italy.

Surattana Sungnul (S)

Department of Mathematics, King Mongkut's University of Technology North Bangkok, Thailand; Centre of Excellence in Mathematics, Bangkok, Thailand.

Elvin J Moore (EJ)

Department of Mathematics, King Mongkut's University of Technology North Bangkok, Thailand; Centre of Excellence in Mathematics, Bangkok, Thailand.

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