1Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
2Population Health Research Institute, Hamilton Health Sciences, Hamilton, Ontario, Canada.
Diabetes Care. 2022 Jan 1;45(1):178-185. doi: 10.2337/dc21-0278.
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.
本研究旨在评估甘精胰岛素、西格列汀/二甲双胍和生活方式干预短期治疗 2 型糖尿病的缓解情况。
在这项开放的多中心试验中,102 例 2 型糖尿病患者被随机分为 1)接受为期 12 周的西格列汀/二甲双胍、甘精胰岛素和生活方式治疗,或 2)对照组。12 周时 HbA1c<7.3%(<56mmol/mol)的患者被要求停止使用糖尿病药物,并在 52 周时随访是否有复发证据。糖尿病复发标准包括 HbA1c≥6.5%(≥48mmol/mol)、1 周内至少 50%的毛细血管血糖读数>10mmol/L、以及重新开始使用糖尿病药物,无论空腹血糖(FPG)或口服葡萄糖耐量试验(OGTT)2 小时血糖是否异常。进行生存时间分析,比较治疗组有(主要分析)和无(补充分析)FPG/OGTT 复发标准的结果。
纳入 FPG/OGTT 复发标准后,与对照组相比,干预组的复发风险比(HR)为 0.72(95%CI 0.47-1.10)(主要分析),且治疗组在 24、36、48 和 64 周时缓解的患者数量无显著差异。在不纳入这些标准的补充分析中,复发的 HR 为 0.60(95%CI 0.39-0.95),且干预组在 36 周时缓解的患者数量显著更高(26%比 10%)。
尽管我们的主要结局无统计学意义,但这种方法值得进一步研究,并进一步优化其组成部分。