Evidence map›Paper›PMID 23911175›Full record

ArticleJournal of diabetes science and technology2013

A composite model of glucagon-glucose dynamics for in silico testing of bihormonal glucose controllers.

Pau Herrero, Pantelis Georgiou, Nick Oliver, Monika Reddy, Desmond Johnston, Christofer Toumazou

Registry-linked trialAbstract read
In one paragraph

Article in Journal of diabetes science and technology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02397265 (Clinical Assessment of a Closed-loop System With Glucagon, Exercise and Mixed Meals), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02397265 nacompletednot on this mapstarted 2014, after this paper: background citation

Clinical Assessment of a Closed-loop System With Glucagon, Exercise and Mixed Meals

TypeinterventionalSponsorImperial College LondonRan2014 to 2015Enrolled24ConditionsType 1 DiabetesArmsBi-hormonal closed loop pump, Standard opened loop pump, Insulin closed loop
3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Modeling the effect of glucagon on endogenous glucose production in healthy individuals under meal-like conditions.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  2. Artificial pancreas: the past and the future.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2025
    Review
  3. Article
  4. Article
  5. Nonlinear Mixed Effects Modeling of Glucagon Kinetics in Healthy Subjects.IEEE transactions on bio-medical engineering · 2023
    Article
  6. Modelling the effects of glucagon during glucose tolerance testing.Theoretical biology & medical modelling · 2019
    Article
  7. Mathematical modeling of the glucagon challenge test.Journal of pharmacokinetics and pharmacodynamics · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. A coordinated control strategy for insulin and glucagon delivery in type 1 diabetes.Computer methods in biomechanics and biomedical engineering · 2017
    Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Pau HerreroCenter for Bio-Inspired Technology, Department of Electrical and Electronic Engineering, Institute of Biomedical Engineering, Imperial College London, South Kensington Campus, London, UK. pherrero@imperial.ac.uk
Pantelis Georgiou
Nick Oliver
Monika Reddy
Desmond Johnston
Christofer Toumazou

Funding

Wellcome Trust 100921
6 · The paper itself

Abstract

backgroundThe utility of simulation environments in the development of an artificial pancreas for type 1 diabetes mellitus (T1DM) management is well established. The availability of a simulator that incorporates glucagon as a counterregulatory hormone to insulin would allow more efficient design of bihormonal glucose controllers. Existing models of the glucose regulatory system that incorporates glucagon action are difficult to identify without using tracer data. In this article, we present a novel model of glucagon-glucose dynamics that can be easily identified with standard clinical research data.

methodsThe minimal model of plasma glucose and insulin kinetics was extended to account for the action of glucagon on net endogenous glucose production by incorporating a new compartment. An existing subcutaneous insulin absorption model was used to account for subcutaneous insulin delivery. The same model of insulin pharmacokinetics was employed to model the pharmacokinetics of subcutaneous glucagon absorption. Finally, we incorporated an existing gastrointestinal absorption model to account for meal intake. Data from a closed-loop artificial pancreas study using a bihormonal controller on T1DM subjects were employed to identify the composite model. To test the validity of the proposed model, a bihormonal controller was designed using the identified model.

resultsModel parameters were identified with good precision, and an excellent fitting of the model with the experimental data was achieved. The proposed model allowed the design of a bihormonal controller and demonstrated its ability to improve glycemic control over a single-hormone controller.

conclusionsA novel composite model, which can be easily identified with standard clinical data, is able to account for the effect of exogenous insulin and glucagon infusion on glucose dynamics. This model represents another step toward the development of a bihormonal artificial pancreas.

Indexed as

Computer SimulationModels, BiologicalAlgorithmsBlood GlucoseBlood Glucose Self-MonitoringComputational BiologyDiabetes Mellitus, Type 1GlucagonHumansInsulinInsulin Infusion SystemsBlood GlucoseGlucagonInsulin

Identifiers

PMID23911175
PMCPMC3879758

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.