TY - JOUR
T1 - Type 2 diabetes remission after initiation of GLP-1 receptor agonists
T2 - frequency, characteristics, and outcomes using multiple definitions in an observational study
AU - Fadini, Gian Paolo
AU - Giaccari, Andrea
AU - Broglio, Fabio
AU - Nollino, Laura
AU - Fattor, Bruno
AU - Anichini, Roberto
AU - Meregalli, Giancarla
AU - Avogaro, Angelo
AU - Consoli, Agostino
AU - GLIMPLES study investigators
N1 - Lehr-KH zienda Sanitaria dell'Alto Adige, Bolzano, Italy
PY - 2025/12
Y1 - 2025/12
N2 - Background Remission of type 2 diabetes (T2D) is becoming feasible with modern treatments, including GLP-1 receptor agonists (GLP-1RA). Here, we explored frequency, characteristics, and outcomes associated with various definitions of remission after initiation of GLP-1RA. Methods This was an observational study on new-users of GLP-1RA. We explored 4 definitions of remission: (1) HbA1c to <6.5% persisting >= 3 months in the absence of diabetes pharmacotherapy; (2) As in 1, but allowing GLP-1RA therapy; (3) As in 1, but without new diabetes pharmacotherapy; (4) As in 1, but irrespectively of ongoing diabetes pharmacotherapy. Findings We included 14,141 participants initiating GLP-1RA (60% men, 60-year-old, with a diabetes duration of similar to 10 years, BMI 32 kg/m2, HbA1c 8.1%). The mean observation was 4 years. Remission frequencies by definition were: (1) 5.8%; (2) 6.2%; (3) 12.2%; (4) 18.3%. Duration was shorter for remission 1-2 (5-6 months) than for remission 3-4 (9-10 months). Factors associated with remission were similar across definitions (shorter diabetes duration, higher BMI, lower burden of complications and medications). Remission was associated with significant and sustained benefits on HbA1c (-1%) and body weight (-2 kg). Microvascular events were reduced by 12-16% in participants with remission 1, 2 or 3. Cardiovascular events were reduced only in remission 3 (HR 0.65; 95% C.I. 0.48-0.88). Interpretation T2D remission is not rare after initiation GLP-1RA, its frequency and duration varying by definition. When achieved, remission is associated with durable metabolic improvements up to 4 years and fewer incident complications. Funding Supported by the Italian Diabetes Society (Society Italiana di Diabetologia). (c) 2025 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license
AB - Background Remission of type 2 diabetes (T2D) is becoming feasible with modern treatments, including GLP-1 receptor agonists (GLP-1RA). Here, we explored frequency, characteristics, and outcomes associated with various definitions of remission after initiation of GLP-1RA. Methods This was an observational study on new-users of GLP-1RA. We explored 4 definitions of remission: (1) HbA1c to <6.5% persisting >= 3 months in the absence of diabetes pharmacotherapy; (2) As in 1, but allowing GLP-1RA therapy; (3) As in 1, but without new diabetes pharmacotherapy; (4) As in 1, but irrespectively of ongoing diabetes pharmacotherapy. Findings We included 14,141 participants initiating GLP-1RA (60% men, 60-year-old, with a diabetes duration of similar to 10 years, BMI 32 kg/m2, HbA1c 8.1%). The mean observation was 4 years. Remission frequencies by definition were: (1) 5.8%; (2) 6.2%; (3) 12.2%; (4) 18.3%. Duration was shorter for remission 1-2 (5-6 months) than for remission 3-4 (9-10 months). Factors associated with remission were similar across definitions (shorter diabetes duration, higher BMI, lower burden of complications and medications). Remission was associated with significant and sustained benefits on HbA1c (-1%) and body weight (-2 kg). Microvascular events were reduced by 12-16% in participants with remission 1, 2 or 3. Cardiovascular events were reduced only in remission 3 (HR 0.65; 95% C.I. 0.48-0.88). Interpretation T2D remission is not rare after initiation GLP-1RA, its frequency and duration varying by definition. When achieved, remission is associated with durable metabolic improvements up to 4 years and fewer incident complications. Funding Supported by the Italian Diabetes Society (Society Italiana di Diabetologia). (c) 2025 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license
U2 - 10.1016/j.lanepe.2025.101499
DO - 10.1016/j.lanepe.2025.101499
M3 - Original Article
C2 - 41142657
SN - 2666-7762
VL - 59
SP - 101499
JO - The Lancet regional health. Europe
JF - The Lancet regional health. Europe
M1 - 101499
ER -