Remission of Type 2 Diabetes Following a Short-term Intensive Intervention With Insulin Glargine, Sitagliptin, and Metformin: Results of an Open-label Randomized Parallel-Design Trial

医学 磷酸西他列汀 甘精胰岛素 内科学 二甲双胍 2型糖尿病 糖尿病 危险系数 随机对照试验 胃肠病学 内分泌学 胰岛素 置信区间
作者
Natalia McInnes,Stephanie Hall,Irene Hramiak,Ronald J. Sigal,Ronald Goldenberg,Nikhil Gupta,Rémi Rabasa‐Lhoret,Manoela Braga,Vincent Woo,Farah Sultan,R. Otto,Ada Smith,Diana Sherifali,Yan Yun Liu,Hertzel C. Gerstein
出处
期刊:Diabetes Care [American Diabetes Association]
卷期号:45 (1): 178-185 被引量:9
标识
DOI:10.2337/dc21-0278
摘要

The aim of the study was to evaluate remission of type 2 diabetes following a short-term intervention with insulin glargine, sitagliptin/metformin, and lifestyle approaches.In this open multicenter trial, 102 patients with type 2 diabetes were randomized to 1) a 12-week intervention with sitagliptin/metformin, insulin glargine, and lifestyle therapy or 2) control group. Participants with HbA1c <7.3% (<56 mmol/mol) at 12 weeks were asked to stop diabetes medications and were followed for evidence of relapse over 52 weeks. Diabetes relapse criteria included HbA1c ≥6.5% (≥48 mmol/mol), ≥50% of capillary glucose readings >10 mmol/L over 1 week, and reinitiation of diabetes medications with or without abnormal fasting plasma glucose (FPG) or 2-h plasma glucose on an oral glucose tolerance test (OGTT). Time-to-relapse analysis was conducted to compare the treatment groups with (primary analysis) and without (supplementary analysis) FPG/OGTT relapse criteria.With the FPG/OGTT relapse criteria included, the hazard ratio (HR) of relapse was 0.72 (95% CI 0.47-1.10) in the intervention group compared with the control group (primary analysis), and the number of participants remaining in remission was not significantly different between treatment groups at 24, 36, 48, and 64 weeks. In the supplementary analyses without these criteria, HR of relapse was 0.60 (95% CI 0.39-0.95), and the number of participants remaining in remission was significantly higher (26 vs. 10%) in the intervention group at 36 weeks.Although our primary outcome was not statistically significant, the tested approach deserves further study with further optimization of its components.
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