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A new general glucose homeostatic model using a proportional-integral-derivative controller
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Watson, E. M., Chappell, M. J. (Michael J.), Ducrozet, F., Poucher, S. M. and Yates, J. W. T.. (2011) A new general glucose homeostatic model using a proportional-integral-derivative controller. Computer Methods and Programs in Biomedicine, Vol.102 (No.2). pp. 119-129. ISSN 0169-2607
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WRAP_Chappell_0873262-es-060312-report.pdf - Submitted Version - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader Download (625Kb) |
Official URL: http://dx.doi.org/10.1016/j.cmpb.2010.08.013
Abstract
The glucose-insulin system is a challenging process to model due to the feedback mechanisms present, hence the implementation of a model-based approach to the system is an on-going and challenging research area. A new approach is proposed here which provides an effective way of characterising glycaemic regulation. The resulting model is built on the premise that there are three phases of insulin secretion, similar to those seen in a proportional-integral-derivative (PID) type controller used in engineering control problems. The model relates these three phases to a biological understanding of the system, as well as the logical premise that the homeostatic mechanisms will maintain very tight control of the system. It includes states for insulin, glucose, insulin action and a state to simulate an integral function of glucose. Structural identifiability analysis was performed on the model to determine whether a unique set of parameter values could be identified from the available observations, which should permit meaningful conclusions to be drawn from parameter estimation. Although two parameters - glucose production rate and the proportional control coefficient - were found to be unidentifiable, the former is not a concern as this is known to be impossible to measure without a tracer experiment, and the latter can be easily estimated from other means. Subsequent parameter estimation using Intravenous Glucose Tolerance Test (IVGTT) and hyperglycaemic clamp data was performed and subsequent model simulations have shown good agreement with respect to these real data.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QP Physiology |
| Divisions: | Faculty of Science > Engineering |
| Library of Congress Subject Headings (LCSH): | Insulin -- Synthesis -- Regulation -- Mathematical models |
| Journal or Publication Title: | Computer Methods and Programs in Biomedicine |
| Publisher: | Elsevier Ireland Ltd. |
| ISSN: | 0169-2607 |
| Date: | May 2011 |
| Volume: | Vol.102 |
| Number: | No.2 |
| Page Range: | pp. 119-129 |
| Identification Number: | 10.1016/j.cmpb.2010.08.013 |
| Status: | Peer Reviewed |
| Publication Status: | Published |
| Access rights to Published version: | Restricted or Subscription Access |
| Funder: | AstraZeneca (Firm) |
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| URI: | http://wrap.warwick.ac.uk/id/eprint/35455 |
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