GLP-1 Receptor Agonists Models for Type 1 Diabetes: A Narrative Review

被引:0
|
作者
Furio-Novejarque, Clara [1 ]
Diez, Jose-Luis [1 ,2 ]
Bondia, Jorge [1 ,2 ]
机构
[1] Univ Politecn Valencia, Inst Univ Automat & Informat Ind, Cami Vera S-N, Valencia 46022, Spain
[2] Inst Salud Carlos III, Ctr Invest Biomed Red Diabet & Enfermedades Metab, Madrid, Spain
来源
关键词
GLP-1; mathematical model; pharmacokinetics; pharmacodynamics; review; simulation; INSULIN; EXENATIDE; GLUCOSE; PHARMACODYNAMICS; LIRAGLUTIDE; EXENDIN-4; MEAL;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Glucagon-like peptide 1 (GLP-1) is a hormone that promotes insulin secretion, delays gastric emptying, and inhibits glucagon secretion. The GLP-1 receptor agonists have been developed as adjunctive therapies for type 2 diabetes to improve glucose control. Recently, there has been an interest in introducing GLP-1 receptor agonists as adjunctive therapies in type 1 diabetes alongside automatic insulin delivery systems. The preclinical validation of these systems often relies on mathematical simulators that replicate the glucose dynamics of a person with diabetes. This review aims to explore mathematical models available in the literature to describe GLP-1 effects to be used in a type 1 diabetes simulator. Methods: Three databases were examined in the search for GLP-1 mathematical models. More than 1500 works were found after searching for specific keywords that were narrowed down to 39 works for full-text assessment. Results: A total of 23 works were selected describing GLP-1 pharmacokinetics and pharmacodynamics. However, none of the found models was designed for type 1 diabetes. An analysis is included of the available models' features that could be translated into a GLP-1 receptor agonist model for type 1 diabetes. Conclusion: There is a gap in research in GLP-1 receptor agonists mathematical models for type 1 diabetes, which could be incorporated into type 1 diabetes simulators, providing a safe and inexpensive tool to carry out preclinical validations using these therapies.
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收藏
页码:332 / 339
页数:8
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