Dallas Diabetes Research Center at Medical City, Dallas, TX
Boehringer Ingelheim International GmbH, Ingelheim, Germany.
Diabetes Care. 2018 Dec;41(12):2560-2569. doi: 10.2337/dc18-1749. Epub 2018 Oct 4.
To evaluate the safety and efficacy of empagliflozin 10- and 25-mg doses plus a unique lower dose (2.5 mg) as adjunct to intensified insulin in patients with type 1 diabetes (T1D).
The EASE (Empagliflozin as Adjunctive to inSulin thErapy) program ( = 1,707) included two double-blind, placebo-controlled phase 3 trials: EASE-2 with empagliflozin 10 mg ( = 243), 25 mg ( = 244), and placebo ( = 243), 52-week treatment; and EASE-3 with empagliflozin 2.5 mg ( = 241), 10 mg ( = 248), 25 mg ( = 245), and placebo ( = 241), 26-week treatment. Together they evaluated empagliflozin 10 mg and 25 mg, doses currently approved in treatment of type 2 diabetes, and additionally 2.5 mg on 26-week change in glycated hemoglobin (primary end point) and weight, glucose time-in-range (>70 to ≤180 mg/dL), insulin dose, blood pressure, and hypoglycemia.
The observed largest mean placebo-subtracted glycated hemoglobin reductions were -0.28% (95% CI -0.42, -0.15) for 2.5 mg, -0.54% (-0.65, -0.42) for 10 mg, and -0.53% (-0.65, -0.42) for 25 mg (all < 0.0001). Empagliflozin 2.5/10/25 mg doses, respectively, reduced mean weight by -1.8/-3.0/-3.4 kg (all < 0.0001); increased glucose time-in-range by +1.0/+2.9/+3.1 h/day ( < 0.0001 for 10 and 25 mg); lowered total daily insulin dose by -6.4/-13.3/-12.7% (all < 0.0001); and decreased systolic blood pressure by -2.1/-3.9/-3.7 mmHg (all < 0.05). Genital infections occurred more frequently on empagliflozin. Adjudicated diabetic ketoacidosis occurred more with empagliflozin 10 mg (4.3%) and 25 mg (3.3%) but was comparable between empagliflozin 2.5 mg (0.8%) and placebo (1.2%). Severe hypoglycemia was rare and frequency was similar between empagliflozin and placebo.
Empagliflozin improved glycemic control and weight in T1D without increasing hypoglycemia. Ketoacidosis rate was comparable between empagliflozin 2.5 mg and placebo but increased with 10 mg and 25 mg. Ketone monitoring for early ketoacidosis detection and intervention and lower empagliflozin doses may help to reduce this risk.
评估恩格列净 10 毫克和 25 毫克剂量与独特的低剂量(2.5 毫克)联合强化胰岛素治疗 1 型糖尿病(T1D)患者的安全性和疗效。
EASE(恩格列净作为胰岛素治疗的辅助药物)计划(=1707)包括两项双盲、安慰剂对照的 3 期试验:EASE-2 中恩格列净 10 毫克(=243)、25 毫克(=244)和安慰剂(=243),治疗 52 周;EASE-3 中恩格列净 2.5 毫克(=241)、10 毫克(=248)、25 毫克(=245)和安慰剂(=241),治疗 26 周。这两项试验共同评估了恩格列净 10 毫克和 25 毫克,这两种剂量目前均被批准用于治疗 2 型糖尿病,此外还评估了 26 周时 2.5 毫克剂量对糖化血红蛋白(主要终点)和体重、血糖时间范围(>70 至≤180mg/dL)、胰岛素剂量、血压和低血糖的影响。
观察到的最大平均安慰剂校正后糖化血红蛋白降低分别为 2.5 毫克组为-0.28%(95%CI-0.42,-0.15)、10 毫克组为-0.54%(-0.65,-0.42)和 25 毫克组为-0.53%(-0.65,-0.42)(均<0.0001)。恩格列净 2.5/10/25 毫克剂量分别使平均体重降低-1.8/-3.0/-3.4kg(均<0.0001);增加葡萄糖时间范围+1.0/+2.9/+3.1h/天(10 毫克和 25 毫克组均<0.0001);降低总日胰岛素剂量-6.4/-13.3/-12.7%(均<0.0001);降低收缩压-2.1/-3.9/-3.7mmHg(均<0.05)。恩格列净组更常发生生殖器感染。恩格列净 10 毫克(4.3%)和 25 毫克(3.3%)组发生糖尿病酮症酸中毒的比例高于安慰剂组(1.2%),但恩格列净 2.5 毫克组(0.8%)与安慰剂组(1.2%)之间无显著差异。严重低血糖罕见,且恩格列净与安慰剂组之间的频率相似。
恩格列净改善了 T1D 患者的血糖控制和体重,且不会增加低血糖的发生风险。恩格列净 2.5 毫克和安慰剂组的酮症酸中毒发生率相当,但 10 毫克和 25 毫克组的发生率较高。通过酮体监测及早发现和干预酮症酸中毒,并降低恩格列净的剂量,可能有助于降低这种风险。