Bonadonna Riccardo C, Mauricio Didac, Müller-Wieland Dirk, Freemantle Nick, Bigot Gregory, Mauquoi Celine, Ciocca Alice, Bonnemaire Mireille, Gourdy Pierre
Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.
Department of Medicine and Surgery, University of Parma, Parma, Italy.
Diabetes Ther. 2021 Apr;12(4):1073-1097. doi: 10.1007/s13300-021-01030-0. Epub 2021 Mar 1.
Patients aged ≥ 65 years continue to be underrepresented in clinical studies related to type 2 diabetes mellitus (T2DM). Accordingly, the REALI pooled analysis was performed to evaluate the effectiveness and safety of insulin glargine 300 U/mL (Gla-300) across different age subgroups, using data from 14 interventional and non-interventional studies.
Pooled efficacy and safety data were collected from 8106 European patients with uncontrolled T2DM who were initiated on or switched to Gla-300 injected once daily for 24 weeks. Patients were categorised into five age subgroups: < 50 (N = 727), 50-59 (N = 2030), 60-69 (N = 3054), 70-79 (N = 1847) and ≥ 80 years (N = 448).
Mean baseline haemoglobin A1c (HbA1c) decreased linearly from the youngest (9.10%) to the oldest (8.46%) age subgroup. Following Gla-300 initiation, there were similar HbA1c reductions across age groups, with a least squares mean (95% confidence interval) change in HbA1c from baseline to week 24 of - 1.09% (- 1.18 to - 1.00), - 1.08% (- 1.14 to - 1.03), - 1.12% (- 1.17 to - 1.07), - 1.18% (- 1.24 to - 1.12) and - 1.11% (- 1.23 to - 0.99) in the < 50, 50-59, 60-69, 70-79 and ≥ 80 years subgroups, respectively. The incidences and event rates of reported hypoglycaemia were overall low. Compared to younger age subgroups, lower incidences of symptomatic hypoglycaemia occurring at any time of the day (5.9 vs. 7.6-9.4% for the younger subgroups) or during the night (0.5 vs. 1.6-2.5%) were recorded in patients aged ≥ 80 years. By contrast, the highest incidence of severe hypoglycaemia occurring any time of the day was reported in the subgroup aged ≥ 80 years (1.1 vs. 0.1-0.6% for the younger age subgroups).
Gla-300 initiated in patients with uncontrolled T2DM provides glycaemic improvement with a favourable safety profile across a wide range of ages.
在2型糖尿病(T2DM)相关临床研究中,65岁及以上患者的代表性仍然不足。因此,开展了REALI汇总分析,利用14项干预性和非干预性研究的数据,评估不同年龄亚组中甘精胰岛素300 U/mL(Gla-300)的有效性和安全性。
收集了8106例欧洲T2DM控制不佳患者的汇总疗效和安全性数据,这些患者开始使用或换用Gla-300,每日注射1次,共24周。患者被分为五个年龄亚组:<50岁(N = 727)、50-59岁(N = 2030)、60-69岁(N = 3054)、70-79岁(N = 1847)和≥80岁(N = 448)。
平均基线糖化血红蛋白(HbA1c)从最年轻的年龄亚组(9.10%)到最年长的年龄亚组(8.46%)呈线性下降。开始使用Gla-300后,各年龄组的HbA1c降低情况相似,从基线到第24周HbA1c的最小二乘均值(95%置信区间)变化在<50岁、50-59岁、60-69岁、70-79岁和≥80岁亚组中分别为-1.09%(-1.18至-1.00)、-1.08%(-1.14至-1.03)、-1.12%(-1.17至-1.07)、-1.18%(-1.24至-1.12)和-1.11%(-1.23至-0.99)。报告的低血糖发生率和事件率总体较低。与较年轻的年龄亚组相比,≥80岁患者在一天中任何时间(5.9% vs. 较年轻亚组的7.6-9.4%)或夜间(0.5% vs. 1.6-2.5%)发生症状性低血糖的发生率较低。相比之下,≥80岁亚组报告的一天中任何时间严重低血糖的发生率最高(1.1% vs. 较年轻年龄亚组的0.1-0.6%)。
在T2DM控制不佳的患者中起始使用Gla-300可改善血糖,在广泛的年龄范围内具有良好的安全性。