Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jtbi.2016.12.018
Title: Personalized glucose-insulin model based on signal analysis
Authors: Goede S.L.
de Galan B.E.
Leow M.K.S. 
Keywords: Appearance profile
Electrical network model
Model identification
Personalized target
Simulation
Validation
Issue Date: 2017
Publisher: Academic Press
Citation: Goede S.L., de Galan B.E., Leow M.K.S. (2017). Personalized glucose-insulin model based on signal analysis. Journal of Theoretical Biology 419 : 333 - 342. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jtbi.2016.12.018
Abstract: Glucose plasma measurements for diabetes patients are generally presented as a glucose concentration-time profile with 15?60 min time scale intervals. This limited resolution obscures detailed dynamic events of glucose appearance and metabolism. Measurement intervals of 15 min or more could contribute to imperfections in present diabetes treatment. High resolution data from mixed meal tolerance tests (MMTT) for 24 type 1 and type 2 diabetes patients were used in our present modeling. We introduce a model based on the physiological properties of transport, storage and utilization. This logistic approach follows the principles of electrical network analysis and signal processing theory. The method mimics the physiological equivalent of the glucose homeostasis comprising the meal ingestion, absorption via the gastrointestinal tract (GIT) to the endocrine nexus between the liver, pancreatic alpha and beta cells. This model demystifies the metabolic ?black box? by enabling in silico simulations and fitting of individual responses to clinical data. Five-minute intervals MMTT data measured from diabetic subjects result in two independent model parameters that characterize the complete glucose system response at a personalized level. From the individual data measurements, we obtain a model which can be analyzed with a standard electrical network simulator for diagnostics and treatment optimization. The insulin dosing time scale can be accurately adjusted to match the individual requirements of characterized diabetic patients without the physical burden of treatment. ? 2017 Elsevier Ltd
Source Title: Journal of Theoretical Biology
URI: https://scholarbank.nus.edu.sg/handle/10635/177443
ISSN: 00225193
DOI: 10.1016/j.jtbi.2016.12.018
Appears in Collections:Staff Publications

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