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Two-Year Real-Life Achievements of MiniMed 780G Advanced Closed-Loop System in Youth with Type 1 Diabetes: AWeSoMe Study Group Multicenter Prospective Extended Follow-Up.

Created on 19 Aug 2026

Authors

Yael Lebenthal, Talia Jacobi-Polishook, Shirli Abiri, Kineret Mazor-Aronovitch, Avivit Brener, Tal Ben Ari, Neriya Levran, Noah Levek, Avigail Wittenberg, Zohar Landau, Marianna Rachmiel, Orit Pinhas-Hamiel, Noah Gruber

Published in

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. Aug 18, 2026. Epub Aug 18, 2026.

Abstract

To determine whether glycemic benefits of the MiniMed 780G Advanced Hybrid Closed-Loop (AHCL) system are sustained over two years in youth with type 1 diabetes (T1D), and to identify outcome predictors.
This prospective multicenter study collected CGM and clinical data at 1,3,6,12, and 24 months in 96 children and adolescents with T1D. Outcomes included HbA1c, CGM metrics, composite glycemic control (CGC) score, glycemia risk index (GRI), composite CGM index (COGI), SmartGuard use, and anthropometric changes, analyzed by repeated-measures linear mixed models.
HbA1c and time in range were maintained from 12 to 24 months, but time below range increased (1.8% to 2.5%, P=0.015). Composite targets were rarely met: CGC by 14.6%, best GRI by 9.4%, best COGI by 10.4%. SmartGuard use declined from 91.3% to 82.7% (P=0.013); lower socioeconomic position and lower 12-month SmartGuard use were independently associated with this decline. Girls had lower glycemic variability than boys and greater BMI z-score increase. Five DKA and two severe hypoglycemia events occurred, all device-or behavior-related.
The 780G AHCL system sustained meaningful glycemic benefits over two years, yet most youth failed to achieve optimal composite glycemic control. SmartGuard decline during the second year suggests the 12-month visit as a candidate checkpoint for monitoring device engagement, warranting evaluation in a future interventional trial.

PMID:
42612909
Bibliographic data and abstract were imported from PubMed on 19 Aug 2026.

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