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

Overview of attention for article published in BioMedical Engineering OnLine, March 2015
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Title
Modelling endogenous insulin concentration in type 2 diabetes during closed-loop insulin delivery
Published in
BioMedical Engineering OnLine, March 2015
DOI 10.1186/s12938-015-0009-5
Pubmed ID
Authors

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

Abstract

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. 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. 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). 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.

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Mendeley readers

The data shown below were compiled from readership statistics for 76 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 1%
Unknown 75 99%

Demographic breakdown

Readers by professional status Count As %
Student > Master 17 22%
Researcher 10 13%
Student > Bachelor 10 13%
Student > Ph. D. Student 8 11%
Other 5 7%
Other 12 16%
Unknown 14 18%
Readers by discipline Count As %
Medicine and Dentistry 19 25%
Engineering 13 17%
Nursing and Health Professions 5 7%
Agricultural and Biological Sciences 4 5%
Computer Science 3 4%
Other 18 24%
Unknown 14 18%