{"title":"在自动胰岛素输送(AID)系统中使用更快的胰岛素类似物的计算机评估,无需膳食公告","authors":"Marcela Moscoso-Vasquez , Marc D. Breton","doi":"10.1016/j.ifacol.2025.06.004","DOIUrl":null,"url":null,"abstract":"<div><div>Automated Insulin delivery has become standard of care for managing glycemic control in Type 1 Diabetes (T1D), and has been shown to dramatically improve overall glycemic control. However, postprandial hyperglycemia remains a challenge, even with AID systems that require meal announcements. Rapid- and Ultra-rapid-acting insulin analogs that could improve or even prevent postprandial hyperglycemia are now available for both research and clinical care. However, it has been shown that adjusting AID system’s parameters is necessary for maximizing benefits when using accelerated insulins within these systems. In this work, the safety and performance effect of accelerating insulin within AIDANET, a state-of-the-art AID system is evaluated in-silico to address postprandial hyperglycemia generated by unannounced meals. Pharmacokinetic parameters are leveraged to include the use of a novel ultra-rapid insulin formulation within the UVA/Padova Type 1 Diabetes simulator. Additionally, two in-silico scenarios are used to assess the performance of Automated Insulin Delivery as Adaptive NETwork (AIDANET) with (i) faster insulin analogs and (ii) more concentrated formulations. Results show that AIDANET’s built-in adaptive capabilities allow it to adjust its aggressiveness to accommodate faster PK and more concentrated formulations, achieving clinically significant improvements in glycemic control outcomes and maximizing the benefits of alternative formulations.</div></div>","PeriodicalId":37894,"journal":{"name":"IFAC-PapersOnLine","volume":"59 2","pages":"Pages 19-24"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In-silico Assessment of Using Faster Insulin Analogs in Automated Insulin Delivery (AID) Systems Without Meal Announcement⁎\",\"authors\":\"Marcela Moscoso-Vasquez , Marc D. Breton\",\"doi\":\"10.1016/j.ifacol.2025.06.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Automated Insulin delivery has become standard of care for managing glycemic control in Type 1 Diabetes (T1D), and has been shown to dramatically improve overall glycemic control. However, postprandial hyperglycemia remains a challenge, even with AID systems that require meal announcements. Rapid- and Ultra-rapid-acting insulin analogs that could improve or even prevent postprandial hyperglycemia are now available for both research and clinical care. However, it has been shown that adjusting AID system’s parameters is necessary for maximizing benefits when using accelerated insulins within these systems. In this work, the safety and performance effect of accelerating insulin within AIDANET, a state-of-the-art AID system is evaluated in-silico to address postprandial hyperglycemia generated by unannounced meals. Pharmacokinetic parameters are leveraged to include the use of a novel ultra-rapid insulin formulation within the UVA/Padova Type 1 Diabetes simulator. Additionally, two in-silico scenarios are used to assess the performance of Automated Insulin Delivery as Adaptive NETwork (AIDANET) with (i) faster insulin analogs and (ii) more concentrated formulations. Results show that AIDANET’s built-in adaptive capabilities allow it to adjust its aggressiveness to accommodate faster PK and more concentrated formulations, achieving clinically significant improvements in glycemic control outcomes and maximizing the benefits of alternative formulations.</div></div>\",\"PeriodicalId\":37894,\"journal\":{\"name\":\"IFAC-PapersOnLine\",\"volume\":\"59 2\",\"pages\":\"Pages 19-24\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IFAC-PapersOnLine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2405896325003088\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IFAC-PapersOnLine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405896325003088","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Engineering","Score":null,"Total":0}
In-silico Assessment of Using Faster Insulin Analogs in Automated Insulin Delivery (AID) Systems Without Meal Announcement⁎
Automated Insulin delivery has become standard of care for managing glycemic control in Type 1 Diabetes (T1D), and has been shown to dramatically improve overall glycemic control. However, postprandial hyperglycemia remains a challenge, even with AID systems that require meal announcements. Rapid- and Ultra-rapid-acting insulin analogs that could improve or even prevent postprandial hyperglycemia are now available for both research and clinical care. However, it has been shown that adjusting AID system’s parameters is necessary for maximizing benefits when using accelerated insulins within these systems. In this work, the safety and performance effect of accelerating insulin within AIDANET, a state-of-the-art AID system is evaluated in-silico to address postprandial hyperglycemia generated by unannounced meals. Pharmacokinetic parameters are leveraged to include the use of a novel ultra-rapid insulin formulation within the UVA/Padova Type 1 Diabetes simulator. Additionally, two in-silico scenarios are used to assess the performance of Automated Insulin Delivery as Adaptive NETwork (AIDANET) with (i) faster insulin analogs and (ii) more concentrated formulations. Results show that AIDANET’s built-in adaptive capabilities allow it to adjust its aggressiveness to accommodate faster PK and more concentrated formulations, achieving clinically significant improvements in glycemic control outcomes and maximizing the benefits of alternative formulations.
期刊介绍:
All papers from IFAC meetings are published, in partnership with Elsevier, the IFAC Publisher, in theIFAC-PapersOnLine proceedings series hosted at the ScienceDirect web service. This series includes papers previously published in the IFAC website.The main features of the IFAC-PapersOnLine series are: -Online archive including papers from IFAC Symposia, Congresses, Conferences, and most Workshops. -All papers accepted at the meeting are published in PDF format - searchable and citable. -All papers published on the web site can be cited using the IFAC PapersOnLine ISSN and the individual paper DOI (Digital Object Identifier). The site is Open Access in nature - no charge is made to individuals for reading or downloading. Copyright of all papers belongs to IFAC and must be referenced if derivative journal papers are produced from the conference papers. All papers published in IFAC-PapersOnLine have undergone a peer review selection process according to the IFAC rules.