Leiter Lawrence A, Shestakova Marina V, Satman Ilhan
1Division of Endocrinology & Metabolism, Li Ka Shing Knowledge Institute of St. Michael's Hospital, University of Toronto, 61 Queen Street East, #6121Q, Toronto, ON M5C 2T2 Canada.
2Institute of Diabetes Mellitus, Endocrinology Research Centre and M.I. Sechenov First Moscow State Medical University, Moscow, Russian Federation.
Diabetol Metab Syndr. 2018 Apr 10;10:30. doi: 10.1186/s13098-018-0331-8. eCollection 2018.
Although the number of antihyperglycemic agents has expanded significantly, sulfonylureas (in particular gliclazide) remain an important option because of a variety of patient and health system factors. The large, real world, observational, and international EASYDia trial evaluated the effectiveness of gliclazide modified release (MR) 60 mg in individuals with type 2 diabetes with a broad range of diabetes history, body mass index (BMI) and background antihyperglycemic treatment.
A total of 7170 participants from eight countries, age ≥ 35 years with HbA1c ≥ 7.5% and not treated with insulin, were prescribed 30-120 mg of gliclazide MR 60 mg once daily. HbA1c goals were individualized and dosing uptitrated, as required, over the 6-month long study. In this post hoc subanalysis, efficacy endpoints were analyzed according to stratified baseline HbA1c levels, weight and glucose-lowering regimens. Episodes of hypoglycemia requiring assistance were documented.
At baseline, mean age was 58.9 years, HbA1c 8.8%, BMI 30.1 kg/m, and diabetes duration 5.1 years. At study end, clinically significant HbA1c improvements (mean change - 1.78%) were noted across all baseline HbA1c strata (> 7.0 to ≤ 8.0%, > 8.0 to ≤ 9.0%, > 9.0 to ≤ 10.0%, and > 10.0%), BMI classifications (18.5 to < 25.0, 25.0 to < 30.0, and ≥ 30.0 kg/m), and regardless of the original diabetes treatment regimen (< 0.001 in all cases). In contrast to the subgroups with BMI 25.0-30.0 and ≥ 30.0 kg/m that registered weight losses of 0.9 and 2.2 kg, respectively (< 0.001 vs. baseline weight); the BMI 18.5-24.9 kg/m subgroup gained a mean 0.5 kg (< 0.02 vs. baseline weight). Severe hypoglycemic events were rare (0.06%).
Progressive gliclazide MR 60 mg uptitration was well tolerated and lowered HbA1c across a broad range of HbA1c, BMI and background glucose-lowering therapy. Weight loss was noted when BMI was ≥ 25.0 kg/m. Individuals with the highest baseline HbA1c and BMI experienced the greatest HbA1c and weight improvements. ISRCTN Registry ISRCTN00943368 on 1st July 2011.
尽管抗高血糖药物的种类已显著增加,但由于多种患者和卫生系统因素,磺脲类药物(尤其是格列齐特)仍是重要的选择。大型、真实世界、观察性的国际EASYDia试验评估了60毫克缓释格列齐特在具有广泛糖尿病病史、体重指数(BMI)和背景抗高血糖治疗的2型糖尿病患者中的有效性。
来自八个国家的7170名年龄≥35岁、糖化血红蛋白(HbA1c)≥7.5%且未接受胰岛素治疗的参与者,被处方每日一次30 - 120毫克的60毫克缓释格列齐特。HbA1c目标是个体化的,并在为期6个月的研究中根据需要增加剂量。在这项事后亚组分析中,根据分层的基线HbA1c水平、体重和降糖方案分析疗效终点。记录需要协助的低血糖发作情况。
基线时,平均年龄为58.9岁,HbA1c为8.8%,BMI为30.1kg/m²,糖尿病病程为5.1年。研究结束时,在所有基线HbA1c分层(>7.0至≤8.0%、>8.0至≤9.0%、>9.0至≤10.0%以及>10.0%)、BMI分类(18.5至<25.0、25.0至<30.0以及≥30.0kg/m²)中,无论最初的糖尿病治疗方案如何,均观察到具有临床意义的HbA1c改善(平均变化-1.78%)(所有情况均P<0.001)。与BMI为25.0 - 30.0kg/m²和≥30.0kg/m²的亚组分别体重减轻0.9千克和2.2千克相比(与基线体重相比P<0.001);BMI为18.5 - 24.9kg/m²的亚组平均体重增加0.5千克(与基线体重相比P<0.02)。严重低血糖事件罕见(0.06%)。
逐步增加60毫克缓释格列齐特的剂量耐受性良好,在广泛的HbA1c、BMI和背景降糖治疗范围内均可降低HbA1c。当BMI≥25.0kg/m²时出现体重减轻。基线HbA1c和BMI最高的个体HbA1c和体重改善最大。ISRCTN注册号:ISRCTN00943368,于2011年7月1日注册。