Evolution of the Artificial Pancreas: Components and Integration-CGMs, Insulin, and AP Systems.

Jennifer L Sherr, Michael A Weiss, Halis K Akturk, Eyal Dassau, Rayhan Lal, Eric Renard, Roy W Beck, Melissa S Putman, Steven J Russell, Roman Hovorka, Jay S Skyler, Gregory P Forlenza, Susan A Brown, Robert Vigersky, Marc D Breton, Adam Heller, Edward R Damiano, Claudio Cobelli, Richard M Bergenstal

Journal: Journal of diabetes science and technology 2025;19(4):883-894

PMID: 40590461

Abstract

The landmark Diabetes Control and Complications Trial (DCCT) showed that glucose control is critical to reducing the risk of diabetes-related complications. This chapter outlines a series of innovations and investigations that followed the DCCT, aimed at minimizing the risk of hypoglycemia while further improving glucose control. The chapter presents an example of innovations in wired enzyme technology that facilitated the movement from capillary glucose monitoring to continuous glucose monitoring (CGM) and ultimately, the first-factory calibrated CGM system. The next glycemic management innovation was to connect CGM data to an insulin pump containing an algorithm able to adjust insulin delivery based on the changing glucose levels and trends. The key features of automated insulin delivery (AID) systems, currently approved in the United States, are presented. The AID summary table includes type of pump, type and function of the insulin delivery algorithm, the data management system, and the indications for use. The next section explores the innovation of alternative routes of insulin delivery to move toward the goal of a fully automated insulin delivery system. The main trials in developing and implementing an implantable intraperitoneal programmable system are summarized. The last section explores if sensor input in addition to glucose levels such as continuous sensing of ketone, lactate, or insulin levels may provide valuable feedback to move us closer to a fully autonomous AID system. Much of this diabetes innovation and investigation work has been supported by the National Institute of Diabetes and Digestive and Kidney Diseases over that last 75 years.

Address: International Diabetes Center, HealthPartners Institute, Minneapolis, MN, USA.; Independent Researcher, Austin, TX, USA.; TheraSense, Alameda, CA, USA.; University of Virginia, Charlottesville, VA, USA.; Medtronic Diabetes, Northridge, CA, USA.; Barbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.; Division of Pediatric Endocrinology, Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.; Institute of Metabolic Science, University of Cambridge, Cambridge, UK.; Diabetes Clinical Center and Beta Bionics, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.; Department of Biomedical Engineering, Boston University, Boston, MA, USA.; Diabetes Research Center, Mass General Hospital, Boston, MA, USA.; Jaeb Center, Tampa, FL, USA.; Montpellier University Hospital, Institute of Functional Genomics, CNRS, INSERM, University of Montpellier, Montpellier, France.; Division of Endocrinology, Department of Pediatrics and Medicine, Stanford University, Stanford, CA, USA.; University of Padova, Padova, Italy.; Harvard University, Boston, MA, USA.; Department of Biochemistry & Molecular Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.; Diabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
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