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Automated insulin delivery system

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"Artificial pancreas" redirects here. For other uses, see Artificial pancreas (disambiguation).

Automated insulin delivery systems are automated (or semi-automated) systems designed to assist people with diabetes, primarily type 1, by automatically adjusting insulin delivery to help them control their blood glucose levels. Currently available systems (as of October 2020) can only deliver (and regulate delivery of) a single hormone—insulin. Other systems currently in development aim to improve on current systems by adding one or more additional hormones that can be delivered as needed, providing something closer to the endocrine functionality of a healthy pancreas.

The endocrine functionality of the pancreas is provided by islet cells which produce the hormones insulin and glucagon. Artificial pancreatic technology mimics the secretion of these hormones into the bloodstream in response to the body's changing blood glucose levels. Maintaining balanced blood sugar levels is crucial to the function of the brain, liver, and kidneys.[1] Therefore, for type 1 patients, it is necessary that the levels be kept balanced when the body cannot produce insulin itself.[1]

Automated insulin delivery systems are often referred to using the term artificial pancreas, but the term has no precise, universally accepted definition. For uses other than automated insulin delivery, see Artificial pancreas (disambiguation).

General overview

History

The first automated insulin delivery system was known as the Biostator.[citation needed]

Classes of AID systems

Currently available AID systems fall into four broad classes based on their capabilities. The first systems released- suspend systems- can only halt insulin delivery. Loop systems can modulate delivery both up and down.[citation needed]

Threshold suspend

Threshold suspend systems are the simplest form of insulin delivery automation. They halt the constant flow of insulin from a pump (known as basal insulin) when a connected CGM reports a glucose level below a pre-set threshold. Halting basal delivery stops the normal preprogrammed rate of delivery, but it cannot remove insulin that has already been infused, so the overall efficacy of threshold suspend systems is limited due to the relatively slow pharmacokinetics of insulin delivered subcutaneously.[citation needed]

Predictive low glucose suspend

A step forward from threshold suspend systems, predictive low glucose suspend (PLGS) systems use a mathematical model to extrapolate predicted future blood sugar levels based on recent past readings from a CGM. This allows the system to halt insulin delivery as much as 30 minutes prior to a predicted hypoglycemic event, allowing addition time for the slow pharmacokinetics of insulin to reflect that delivery has been halted.

Hybrid closed loop

Hybrid closed loop (HCL) systems further expand on the capabilities of PGLS systems by adjusting basal insulin delivery rates both up and down in response to values from a continuous glucose monitor. Through this modulation of basal insulin, the system is able to reduce the magnitude and duration both hyperglycemic and hypoglycemic events.

Advanced hybrid closed loop

In addition to modulating basal insulin, advanced hybrid closed loop systems have the ability to deliver boluses of insulin to correct for elevated blood sugar.

Required components

An automated insulin delivery system consists of three distinct components: a continuous glucose monitor to determine blood sugar levels, a pump to deliver insulin, and an algorithm that uses the data from the CGM to send commands to the pump. In the United States, the Food and Drug Administration (FDA) allows each component to be approved independently, allowing for more rapid approvals and incremental innovation. Each component is discussed in greater detail below.

Continuous glucose monitor (CGM)

Artificial pancreas feedback system

Continuous glucose monitors (CGMs) are medical devices which extrapolate an estimate of the glucose concentration in a patient's blood based on the level of glucose present in the subcutaneous interstitial fluid. A thin, biocompatible sensor wire coated with a glucose-reactive enzyme is inserted into the skin, allowing the system to read the voltage generated, and based on it, estimate blood glucose. The biggest advantage of a CGM over a traditional fingerstick blood glucose meter is that the CGM can take a new reading as often as every 60 seconds (although most only take a reading every 5 minutes), allowing for a sampling frequency that is able to provide not just a current blood sugar level, but a record of past measurements; allowing computer systems to project past short-term trends into the future, showing patients where their blood sugar levels are likely headed.

Early CGMs were not particularly accurate, but were still useful for observing and recording overall trends and provide warnings in the event of rapid changes in blood glucose readings.

Continuous blood glucose monitors are one of the set of devices that make up an artificial pancreas device system, the other being an insulin pump, and a glucose meter to calibrate the device.[2] Continuous glucose monitors are a more recent breakthrough and have begun to hit the markets for patient use after approval from the FDA. Both the traditional and the continuous monitor require manual insulin delivery or carbohydrate intake depending on the readings from the devices. While the traditional blood glucose meters require the user to prick their finger every few hours to obtain data, continuous monitors use sensors placed just under the skin on the arm or abdomen to deliver blood sugar level data to receivers or smartphone apps as often as every few minutes.[3] The sensors can be used for up to fourteen days. A number of different continuous monitors are currently approved by the FDA.[4]

The first continuous glucose monitor (CGM) was approved in December 2016. Developed by Dexcom, the G5 mobile continuous monitoring system requires users to prick their fingers twice a day (as opposed to the typical average 8 times daily with the traditional meters) in order to calibrate the sensors. The sensors last up to seven days. The device uses Bluetooth technology to warn the user either through a handheld receiver or app on a smartphone if blood glucose levels reach below a certain point. The cost for this device excluding any co-insurance is an estimated $4,800 a year.[4]

The white sensor is fixed to the upper arm and scanned with the reader. The reader is showing (top to bottom) days to replacement of sensor (11), current BG (7,4) & change (-> i.e. steady) and a diagram of the latest BG levels.
Blood glucose meter FreeStyle Libre from Abbott.

Abbott Laboratories' FreeStyle Libre CGM was approved in September 2017. Recently, the technology was modified to support smartphone use through the LibreLink app. This device does not require finger pricks at all and the sensor, placed on the upper arm, lasts 14 days. The estimated cost for this monitor is $1,300 a year.[4]

Dexcom's next G6 model CGM was approved in March 2018, which can last up to ten days and does not need finger prick calibration. Like Medtronic's monitor, it can predict glucose level trends. It is compatible for integration into insulin pumps.[4]

Control algorithm

Insulin pump

Currently Available systems

Commercial

MiniMed 670G

In September 2016, the FDA approved the Medtronic MiniMed 670G, which was the first approved hybrid closed loop system. The device automatically adjusts a patient's basal insulin delivery.[5] It is made up of a continuous glucose monitor, an insulin pump, and a glucose meter for calibration. It automatically functions to modify the level of insulin delivery based on the detection of blood glucose levels by continuous monitor. It does this by sending the blood glucose data through an algorithm that analyzes and makes the subsequent adjustments.[5] The system has two modes. Manual mode lets the user choose the rate at which basal insulin is delivered. Auto mode regulates basal insulin levels from the CGM readings every five minutes.[6]

Tandem Diabetes Care t:Slim X2 with Control IQ

The Tandem Diabetes Care t:Slim X2 was approved by the U.S. Food and Drug Administration in 2019 and is the first insulin pump to be designated as an alternate controller enabled (ACE) insulin pump. ACE insulin pumps allow users to integrate continuous glucose monitors, automated insulin dosing (AID) systems, and other diabetes management devices with the pump to create a personalized diabetes therapy system. Many users of the t:slim X2 integrate the pump with the Dexcom G6, a continuous glucose monitor approved by the FDA in 2018. It was the first CGM authorized for use in an integrated therapy system. The device does not require fingerstick calibrations.[7]

Non-Commercial

There are several non-commercial, non-FDA approved DIY options, built on RileyLink or AndroidAPS[8][9]

Systems in development

iLet Bionic Pancreas

A team at Boston University working in collaboration with Massachusetts General Hospital on a dual hormone artificial pancreas system [10] began clinical trials on their device called the Bionic Pancreas in 2008.[11] In 2016, the Public Benefit Corporation Beta Bionics was formed. In conjunction with the formation of the company, Beta Bionics changed the preliminary name for their device from the Bionic Pancreas to the iLet.[11] The device uses a closed-loop system to deliver both insulin and glucagon in response to sensed blood glucose levels. While not yet approved for public use, the 4th generation iLet prototype, presented in 2017, is around the size of an iPhone, with a touchscreen interface. It contains two chambers for both insulin and glucagon, and the device is configurable for use with only one hormone, or both.[12] [11]

Inreda AP

In collaboration with the Academic Medical Center in Amsterdam, Inreda Diabetic B.V. has developed a closed loop system with insulin and glucagon. The initiator, Robin Koops, started to develop the device in 2004 and ran the first tests on himself. In October 2016 Inreda Diabetic B.V. got the ISO 13485 license, a first requirement to produce its artificial pancreas.[13] The product itself is called Inreda AP, and soon made some highly successful trials. After clinical trials, it received the CE marking, noting that it complies with European regulation, in February 2020.[14]

In October 2020 the health insurance company Menzis and Inreda Diabetic then started a pilot with 100 patients insured by Menzis. These are all patients that face very serious trouble in regulating their blood glucose levels. They now use the Inreda AP instead of the traditional treatment.[15] Another large scale trial with the Inreda AP was set up in July 2021, and should determine whether Dutch health insurance should cover the device for all their insured.[16] A smaller improved version of the Inreda AP is scheduled for release in 2023.

Bigfoot Autonomy

insulin pump will be based on the defunct Asante Snap technology[17] with plans for a mobile device remote interface.[18][19]

Approaches

Medical equipment

The medical equipment approach involves combining a continuous glucose monitor and an implanted insulin pump that can function together with a computer-controlled algorithm to replace the normal function of the pancreas.[20][21][22] The development of continuous glucose monitors has led to the progress in artificial pancreas technology using this integrated system.[23]

Closed-loop systems

Unlike the continuous sensor alone, the closed-loop system requires no user input in response to reading from the monitor; the monitor and insulin pump system automatically delivers the correct amount of hormone calculated from the readings transmitted. The system is what makes up the artificial pancreas device.[2][3]

Current studies

Four studies on different artificial pancreas systems are being conducted starting in 2017 and going into the near future. The projects are funded by the National Institute of Diabetes and Digestive and Kidney Diseases, and are the final part of testing the devices before applying for approval for use. Participants in the studies are able to live their lives at home while using the devices and being monitored remotely for safety, efficacy, and a number of other factors.[24]

The International Diabetes Closed-Loop trial,[25] led by researchers from the University of Virginia, is testing a closed-loop system called inControl, which has a smartphone user interface. 240 people of ages 14 and up are participating for 6 months.[24]

A full-year trial led by researchers from the University of Cambridge started in May 2017 and has enrolled an estimated 150 participants of ages 6 to 18 years.[24] The artificial pancreas system being studied uses a smartphone and has a low glucose feature to improve glucose level control.[26]

The International Diabetes Center in Minneapolis, Minnesota, in collaboration with Schneider Children's Medical Center of Israel, are planning a 6-month study that will begin in early 2019 and will involve 112 adolescents and young adults, ages 14 to 30.[24][27] The main object of the study is to compare the current Medtronic 670G system to a new Medtronic-developed system. The new system has programming that aims to improve glucose control around mealtime, which is still a big challenge in the field.[27]

The current 6-month study led by the Bionic Pancreas team started in mid-2018 and enrolled 312 participants of ages 18 and above.[24]

Physiological

The Bio-artificial pancreas: this diagram shows a cross section of bio-engineered tissue with encapsulated islet cells which deliver endocrine hormones in response to glucose.

The biotechnical company Defymed, based in France, is developing an implantable bio-artificial device called MailPan which features a bio-compatible membrane with selective permeability to encapsulate different cell types, including pancreatic beta cells.[28] The implantation of the device does not require conjunctive immuno-suppressive therapy because the membrane prevents antibodies of the patient from entering the device and damaging the encapsulated cells. After being surgically implanted, the membrane sheet will be viable for years. The cells that the device holds can be produced from stem cells rather than human donors, and may also be replaced over time using input and output connections without surgery.[28][29] Defymed is partially funded by JDRF, formerly known as the Juvenile Diabetes Research Foundation, but is now defined as an organization for all ages and all stages of type 1 diabetes.[30][31]

In November 2018, it was announced that Defymed would partner with the Israel-based Kadimastem, a bio-pharmaceutical company developing stem-cell based regenerative therapies, to receive a two-year grant worth approximately $1.47 million for the development of a bio-artificial pancreas that would treat type 1 diabetes.[28][32] Kadimastem's stem cell technology uses differentiation of human embryonic stem cells to obtain pancreatic endocrine cells. These include insulin-producing beta cells, as well as alpha cells, which produce glucagon. Both cells arrange in islet-like clusters, mimicking the structure of the pancreas.[33] The aim of the partnership is to combine both technologies in a bio-artificial pancreas device, which releases insulin in response to blood glucose levels, to bring to clinical trial stages.[28]

The San Diego, California based biotech company ViaCyte has also developed a product aiming to provide a solution for type 1 diabetes which uses an encapsulation device made of a semi-permeable immune reaction-protective membrane. The device contains pancreatic progenitor cells that have been differentiated from embryonic stem cells.[34][35] After surgical implantation in an outpatient procedure, the cells mature into endocrine cells which arrange in islet-like clusters and mimic the function of the pancreas, producing insulin and glucagon.[36][37] The technology advanced from pre-clinical studies to FDA approval for phase 1 clinical trials in 2014, and presented two-year data from the trial in June 2018.[34][35] They reported that their product, called PEC-Encap, has so far been safe and well tolerated in patients at a dose below therapeutic levels. The encapsulated cells were able to survive and mature after implantation, and immune system rejection was decreased due to the protective membrane. The second phase of the trial will evaluate the efficacy of the product.[34] ViaCyte has also been receiving financial support from JDRF on this project.[37]

Initiatives around the globe

In the United States in 2006, JDRF (formerly the Juvenile Diabetes Research Foundation) launched a multi-year initiative to help accelerate the development, regulatory approval, and acceptance of continuous glucose monitoring and artificial pancreas technology.[38][39]

Grassroots efforts to create and commercialize a fully automated artificial pancreas system have also arisen directly from patient advocates and the diabetes community.[40] Bigfoot Biomedical, a company founded by parents of children with T1D have created algorithms and are developing a closed loop device that monitor blood sugar and appropriately provide insulin.[41]

References

  • Blauw, H.; et al. (2020), "Clinical validation of a bihormonal artificial pancreas", Diabetes Technology & Therapeutics, 22, Mary Ann Liebert, INC 140 Huguenot Street, 3RD FL, NEW ROCHELLE, NY 10801 USA: A36-A37

Notes

  1. ^ a b "The Pancreas and Its Functions | Columbia University Department of Surgery". columbiasurgery.org. Retrieved 2018-11-07.
  2. ^ a b Health, Center for Devices and Radiological. "Artificial Pancreas Device System - What is the pancreas? What is an artificial pancreas device system?". www.fda.gov. Retrieved 2018-11-27.
  3. ^ a b Elleri D, Dunger DB, Hovorka R (November 2011). "Closed-loop insulin delivery for treatment of type 1 diabetes". BMC Medicine. 9 (1): 120. doi:10.1186/1741-7015-9-120. PMC 3229449. PMID 22071283.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  4. ^ a b c d "The First Four Continuous Glucose Monitors". Managed Care magazine. 2018-07-04. Retrieved 2018-11-07.
  5. ^ a b Health, Center for Devices and Radiological. "Recently-Approved Devices - The 670G System - P160017". wayback.archive-it.org. Archived from the original on 2017-01-11. Retrieved 2018-11-07.
  6. ^ "MiniMed 670G Insulin Pump System | World's First Hybrid Closed Loop System". www.medtronicdiabetes.com. Retrieved 2018-11-07.
  7. ^ "FDA authorizes first fully interoperable continuous glucose monitoring system, streamlines review pathway for similar devices". FDA. March 27, 2018. Retrieved 2021-03-04.
  8. ^ Boise, Michelle. "The Guide to DIY Looping". Beyond Type 1. Retrieved 2022-07-10.
  9. ^ Doskicz, RN, BA, Jewels (December 23, 2021). "How to Create Your Own Hybrid Closed-Loop Insulin Pump System". GoodRx Health. Retrieved July 10, 2022.{{cite web}}: CS1 maint: multiple names: authors list (link) CS1 maint: url-status (link)
  10. ^ "bionicpancreas.org". www.bionicpancreas.org. Retrieved 2018-11-07.
  11. ^ a b c "Update on the iLet Bionic Pancreas Closed Loop System". Healthline. Retrieved 2018-11-07.
  12. ^ "Bionic Pancreas Passes Critical Science Hurdle". BU Today. Retrieved 2018-11-07.
  13. ^ "CE certification is halfway!". inreda diabetic. Retrieved 2021-09-26.
  14. ^ Blauw 2020.
  15. ^ "Kunstmatige alvleesklier: meer vrijheid voor mensen met diabetes type 1". Menzis. 6 October 2020. Retrieved 25 September 2021.
  16. ^ diabetestype1 (13 July 2021). "Nieuw onderzoek naar de kunstalvleesklier mogelijk dankzij grote subsidie". diabetestype1. Retrieved 25 September 2021.{{cite web}}: CS1 maint: numeric names: authors list (link)
  17. ^ "Bigfoot Buys Asante Snap Tech for Closed-Loop System | DiabetesMine". Healthline. 2015-06-03. Retrieved 2022-07-10.
  18. ^ "Inside Bigfoot's Diabetes Lair | DiabetesMine". Healthline. 2019-03-25. Retrieved 2022-07-10.
  19. ^ "Bigfoot Vision". www.bigfootbiomedical.com. Retrieved 2022-07-10.
  20. ^ Gingras V, Taleb N, Roy-Fleming A, Legault L, Rabasa-Lhoret R (February 2018). "The challenges of achieving postprandial glucose control using closed-loop systems in patients with type 1 diabetes". Diabetes, Obesity & Metabolism. 20 (2): 245–256. doi:10.1111/dom.13052. PMC 5810921. PMID 28675686.
  21. ^ Uduku C, Oliver N (October 2017). "Pharmacological aspects of closed loop insulin delivery for type 1 diabetes". Current Opinion in Pharmacology. 36: 29–33. doi:10.1016/j.coph.2017.07.006. hdl:10044/1/60321. PMID 28802779.
  22. ^ Graf A, McAuley SA, Sims C, Ulloa J, Jenkins AJ, Voskanyan G, O'Neal DN (March 2017). "Moving Toward a Unified Platform for Insulin Delivery and Sensing of Inputs Relevant to an Artificial Pancreas". Journal of Diabetes Science and Technology. 11 (2): 308–314. doi:10.1177/1932296816682762. PMC 5478040. PMID 28264192.
  23. ^ Apablaza P, Soto N, Codner E (May 2017). "[From insulin pump and continuous glucose monitoring to the artificial pancreas]". Revista Médica de Chile. 145 (5): 630–640. doi:10.4067/S0034-98872017000500011. PMID 28898340.
  24. ^ a b c d e "The Miracle of an Artificial Pancreas". Retrieved 2018-11-28.
  25. ^ Clinical trial number NCT02844517 for "International Diabetes Closed Loop (iDCL) Trial: Research Site Training Protocol" at ClinicalTrials.gov
  26. ^ Clinical trial number NCT02925299 for "Day and Night Closed-loop in Young People With Type 1 Diabetes" at ClinicalTrials.gov
  27. ^ a b Clinical trial number NCT03040414 for "Fuzzy Logic Automated Insulin Regulation" at ClinicalTrials.gov
  28. ^ a b c d "Israeli and French Biotech Companies Partner to Fight Diabetes With Bio-Artificial Pancreas". CTECH - www.calcalistech.com. 2018-11-12. Retrieved 2018-11-28.
  29. ^ "MailPan ® BioArtificial Pancreas | Defymed, advanced therapies inspired for you". Defymed (in French). Retrieved 2018-11-28.
  30. ^ "Innovative Medical Devices for the Treatment of Diabetes, Defymed Strengthens Its Position as a Worldwide Leader". Retrieved 2018-11-28.
  31. ^ Canada, JDRF. "What Does JDRF Stand For?". JDRF Canada. Retrieved 2018-11-28.
  32. ^ "Kadimastem - Stem Cell to Cure Diseases". www.kadimastem.com. Retrieved 2018-11-28.
  33. ^ "Diabetes - Kadimastem". www.kadimastem.com. Retrieved 2018-11-28.
  34. ^ a b c Inc., ViaCyte. "Two-year Data from ViaCyte's STEP ONE Clinical Trial Presented at ADA 2018". www.prnewswire.com. Retrieved 2018-11-29. {{cite web}}: |last= has generic name (help)
  35. ^ a b "PEC‐Encap™ (VC-01™)". Viacyte, Inc. Retrieved 2018-11-29.
  36. ^ "Home". Viacyte, Inc. Retrieved 2018-11-29.
  37. ^ a b Schulz TC (August 2015). "Concise Review: Manufacturing of Pancreatic Endoderm Cells for Clinical Trials in Type 1 Diabetes". Stem Cells Translational Medicine. 4 (8): 927–31. doi:10.5966/sctm.2015-0058. PMC 4511151. PMID 26062982.
  38. ^ "Artificial Pancreas and FDA–The Latest". JDRF. February 9, 2011.
  39. ^ KMorandi says (2017-08-10). "Insurers can profit while improving the lives of people with type 1 diabetes". STAT. Retrieved 2017-08-10.
  40. ^ Hurley, Dan (24 December 2014) [1] WIRED Magazine, Diabetes Patients Are Hacking Their Way Toward a Bionic Pancreas
  41. ^ Knutson, Ryan (8 June 2015) [2] The Wall Street Journal, Computer Experts Deliver Insulin to Diabetic Kids
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