TY - JOUR
T1 - Outpatient Randomized Crossover Automated Insulin Delivery Versus Conventional Therapy with Induced Stress Challenges
AU - Kaur, Ravinder Jeet
AU - Deshpande, Sunil
AU - Pinsker, Jordan E.
AU - Gilliam, Wesley P.
AU - McCrady-Spitzer, Shelly
AU - Zaniletti, Isabella
AU - Desjardins, Donna
AU - Church, Mei Mei
AU - Doyle, Francis J.
AU - Kremers, Walter K.
AU - Dassau, Eyal
AU - Kudva, Yogish C.
N1 - Funding Information:
This work was made possible through collaboration between the JDRF and The Leona M. and Harry B. Helmsley Charitable Trust (2-SRA-2017-503-M-B), and by grants from the National Institutes of Health (DP3DK104057 and DP3DK113511). Product support was provided by Dexcom, Inc. (research discount on CGM sensors, with transmitters provided in-kind) (IIS-2019-017). Tandem t:AP insulin pumps were purchased from Tandem Diabetes Care, Inc., at full price. The funders and device manufacturers had no influence on the design or conduct of the trial and were not involved in data collection or analysis, the writing of the article, or the decision to submit it for publication.
Funding Information:
J.E.P. is currently an employee and shareholder of Tandem Diabetes Care, Inc., The work presented in the article was performed as part of his academic appointment at Sansum Diabetes Research Institute and is independent of his employment with Tandem Diabetes Care. F.J.D. reports product support from Dexcom, Inc., and Tandem Diabetes Care, as well as patent royalties from Insulet Inc., Dexcom, Mode AGC, and Roche, and is a Scientific Advisor to Mode AGC. E.D. is currently an employee and shareholder of Eli Lilly and Company. The work presented in this article was performed as part of ED’s academic appointment and is independent of his employment with Eli Lilly and Company. E.D. reports consulting fees from Eli Lilly; speaker bureau fees from Roche Diabetes Care; and product support from Dexcom, Inc., and Tandem Diabetes Care, as well as patent royalties from Insulet Inc., Dexcom, Mode AGC, and Roche. W.K.K. receives research funding from the NIH, DOD, AstraZeneca, Roche, and Biogen, all unrelated to this study. Y.C.K. has received product support from Dexcom and Roche Diabetes and consulted for Novo Nordisk. No other conflicts of interest relevant to this project are reported for the rest of the authors.
Publisher Copyright:
© Copyright 2022, Mary Ann Liebert, Inc., publishers 2022.
PY - 2022/5
Y1 - 2022/5
N2 - Background: Automated insulin delivery (AID) systems have not been evaluated in the context of psychological and pharmacological stress in type 1 diabetes. Our objective was to determine glycemic control and insulin use with Zone Model Predictive Control (zone-MPC) AID system enhanced for states of persistent hyperglycemia versus sensor-augmented pump (SAP) during outpatient use, including in-clinic induced stress. Materials and Methods: Randomized, crossover, 2-week trial of zone-MPC AID versus SAP in 14 adults with type 1 diabetes. In each arm, each participant was studied in-clinic with psychological stress induction (Trier Social Stress Test [TSST] and Socially Evaluated Cold Pressor Test [SECPT]), followed by pharmacological stress induction with oral hydrocortisone (total four sessions per participant). The main outcomes were 2-week continuous glucose monitor percent time in range (TIR) 70-180 mg/dL, and glucose and insulin outcomes during and overnight following stress induction. Results: During psychological stress, AID decreased glycemic variability percentage by 13.4% (P = 0.009). During pharmacological stress, including the following overnight, there were no differences in glucose outcomes and total insulin between AID and physician-assisted SAP. However, with AID total user-requested insulin was lower by 6.9 U (P = 0.01) for pharmacological stress. Stress induction was validated by changes in heart rate and salivary cortisol levels. During the 2-week AID use, TIR was 74.4% (vs. SAP 63.1%, P = 0.001) and overnight TIR was 78.3% (vs. SAP 63.1%, P = 0.004). There were no adverse events. Conclusions: Zone-MPC AID can reduce glycemic variability and the need for user-requested insulin during pharmacological stress and can improve overall glycemic outcomes. Clinical Trial Identifier NCT04142229.
AB - Background: Automated insulin delivery (AID) systems have not been evaluated in the context of psychological and pharmacological stress in type 1 diabetes. Our objective was to determine glycemic control and insulin use with Zone Model Predictive Control (zone-MPC) AID system enhanced for states of persistent hyperglycemia versus sensor-augmented pump (SAP) during outpatient use, including in-clinic induced stress. Materials and Methods: Randomized, crossover, 2-week trial of zone-MPC AID versus SAP in 14 adults with type 1 diabetes. In each arm, each participant was studied in-clinic with psychological stress induction (Trier Social Stress Test [TSST] and Socially Evaluated Cold Pressor Test [SECPT]), followed by pharmacological stress induction with oral hydrocortisone (total four sessions per participant). The main outcomes were 2-week continuous glucose monitor percent time in range (TIR) 70-180 mg/dL, and glucose and insulin outcomes during and overnight following stress induction. Results: During psychological stress, AID decreased glycemic variability percentage by 13.4% (P = 0.009). During pharmacological stress, including the following overnight, there were no differences in glucose outcomes and total insulin between AID and physician-assisted SAP. However, with AID total user-requested insulin was lower by 6.9 U (P = 0.01) for pharmacological stress. Stress induction was validated by changes in heart rate and salivary cortisol levels. During the 2-week AID use, TIR was 74.4% (vs. SAP 63.1%, P = 0.001) and overnight TIR was 78.3% (vs. SAP 63.1%, P = 0.004). There were no adverse events. Conclusions: Zone-MPC AID can reduce glycemic variability and the need for user-requested insulin during pharmacological stress and can improve overall glycemic outcomes. Clinical Trial Identifier NCT04142229.
KW - Automated insulin delivery
KW - Continuous glucose monitoring
KW - Hyperglycemia
KW - Pharmacological stress
KW - Psychological stress
KW - Type 1 diabetes
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U2 - 10.1089/dia.2021.0436
DO - 10.1089/dia.2021.0436
M3 - Article
C2 - 35049354
AN - SCOPUS:85130003497
SN - 1520-9156
VL - 24
SP - 338
EP - 349
JO - Diabetes Technology and Therapeutics
JF - Diabetes Technology and Therapeutics
IS - 5
ER -