Modelling endogenous insulin concentration in type 2 diabetes during closed-loop insulin delivery

Yue Ruan, Hood Thabit, Malgorzata E Wilinska, Roman Hovorka

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Closed-loop insulin delivery is an emerging treatment for type 1 diabetes (T1D) evaluated clinically and using computer simulations during pre-clinical testing. Efforts to make closed-loop systems available to people with type 2 diabetes (T2D) calls for the development of a new type of simulators to accommodate differences between T1D and T2D. Presented here is the development of a model of posthepatic endogenous insulin concentration, a component omitted in T1D simulators but key for simulating T2D physiology.

Methods: We evaluated six competing models to describe the time course of endogenous insulin concentration as a function of the plasma glucose concentration and time. The models were fitted to data collected in insulin-naive subjects with T2D who underwent two 24-h visits and were treated, in a random order, by either closed-loop insulin delivery or glucose-lowering oral agents. The model parameters were estimated using a Bayesian approach, as implemented in the WinBUGS software. Model selection criteria were used to identify the best model describing our clinical data.

Results: The selected model successfully described endogenous insulin concentration over 24 h in both study periods and provided plausible parameter estimates. Model-derived results were in concordance with a clinical finding which revealed increased posthepatic endogenous insulin concentration during the control study period (P < 0.05). The modelling results indicated that the excess amount of insulin can be attributed to the glucose-independent effect as the glucose-dependent effect was similar between visits (P > 0.05).

Conclusions: A model to describe endogenous insulin concentration in T2D including components of posthepatic glucose-dependent and glucose-independent insulin secretion was identified and validated. The model is suitable to be incorporated in a simulation environment for evaluating closed-loop insulin delivery in T2D.

Original languageEnglish
Article number19
Pages (from-to)1-13
Number of pages13
JournalBioMedical Engineering OnLine
Volume14
Issue number1
DOIs
Publication statusPublished - 4 Mar 2015

Keywords

  • posthepatic endogenous insulin concentration
  • closed-loop insulin delivery
  • simulation
  • modelling
  • insulin secretion
  • type 2 diabetes

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