Evidence map›Paper›PMID 30893335›Full record

ArticlePloS one2019

Optimal regulation of blood glucose level in Type I diabetes using insulin and glucagon.

Afroza Shirin, Fabio Della Rossa, Isaac Klickstein, John Russell, Francesco Sorrentino

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Controlling network ensembles.Nature communications · 2021
    Article
  2. Article
  3. Article
  4. The Role of Glucagon in Glycemic Variability in Type 1 Diabetes: A Narrative Review.Diabetes, metabolic syndrome and obesity : targets and therapy · 2021
    Review
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

5 authors.

Afroza ShirinMechanical Engineering Department, University of New Mexico, Albuquerque, NM 87131, United States of America.ORCID 0000-0002-3929-7206
Fabio Della RossaMechanical Engineering Department, University of New Mexico, Albuquerque, NM 87131, United States of America.
Isaac KlicksteinMechanical Engineering Department, University of New Mexico, Albuquerque, NM 87131, United States of America.
John RussellMechanical Engineering Department, University of New Mexico, Albuquerque, NM 87131, United States of America.
Francesco SorrentinoMechanical Engineering Department, University of New Mexico, Albuquerque, NM 87131, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Glucose-Insulin-Glucagon nonlinear model accurately describes how the body responds to exogenously supplied insulin and glucagon in patients affected by Type I diabetes. Based on this model, we design infusion rates of either insulin (monotherapy) or insulin and glucagon (dual therapy) that can optimally maintain the blood glucose level within desired limits after consumption of a meal and prevent the onset of both hypoglycemia and hyperglycemia. This problem is formulated as a nonlinear optimal control problem, which we solve using the numerical optimal control package [Formula: see text]. Interestingly, in the case of monotherapy, we find the optimal solution is close to the standard method of insulin based glucose regulation, which is to assume a variable amount of insulin half an hour before each meal. We also find that the optimal dual therapy (that uses both insulin and glucagon) is better able to regulate glucose as compared to using insulin alone. We also propose an ad-hoc rule for both the dosage and the time of delivery of insulin and glucagon.

Indexed as

AlgorithmsBlood GlucoseDiabetes Mellitus, Type 1Drug Delivery SystemsGlucagonHumansHyperglycemiaHypoglycemiaHypoglycemic AgentsInsulinInsulin Infusion SystemsNonlinear DynamicsPostprandial PeriodRiskBlood GlucoseGlucagonHypoglycemic AgentsInsulin

Identifiers

PMID30893335
PMCPMC6426249

What OpenQuestion holds

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Registered trials

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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.