Bellido Diego, Abellán Pablo, Ruiz Palomar José Manuel, Álvarez Sintes Rogelio, Nubiolae Andreu, Bellido Virginia, Romero Gracia
Department of Endocrinology and Nutrition, Ferrol Universitary Hospital Complex (CHUF), Ferrol, Spain.
Department of Endocrinology and Nutrition, Castellón General Universitary Hospital, Castellón de la Plana, Spain; Department of Medicine, Universidad Cardenal Herrera-CEU University, CEU Universities, Castellón, Spain.
Curr Ther Res Clin Exp. 2018 Oct 9;89:37-42. doi: 10.1016/j.curtheres.2018.09.001. eCollection 2018.
Basal insulin reduces fasting blood glucose levels, but postprandial blood glucose levels may remain higher. Traditional strategies with rapid insulin intensification can cause hypoglycemic episodes and weight gain. Glucagon-like peptide-1 receptor agonists, such as the short-acting lixisenatide, are able to control postprandial excursions, without weight gain, and with a low risk of hypoglycemic events.
Due to the limited data on the combination of lixisenatide with basal insulin (with or without oral antidiabetes drugs) in clinical practice, this study evaluated changes in parameters associated with glycemic control and anthropometric data after 24 weeks of this therapy intensification.
This was a multicenter, retrospective observational study of 129 patients with type 2 diabetes that was uncontrolled by basal insulin. Their treatment was intensified by the addition of lixisenatide at least 24 weeks before being included in the study. Data were retrospectively collected to determine changes in glycated hemoglobin (HbA1c) levels, blood glucose levels, weight, and body mass index. Adverse reactions and hypoglycemic events were also recorded.
After 24 weeks of therapy intensification with lixisenatide, a significant reduction in HbA1c levels was observed (-1.1%; < 0.001). An HbA1c <7% was achieved in 30.2% of patients, and 17.1% reached an HbA1c <6.5%. There was a reduction in fasting blood glucose (31.8 [60.3] mg/dL; < 0.001) and postprandial blood glucose (55.0 [49] mg/dL; < 0.001) levels, as well as body weight (4.0 [5.4] kg; < 0.001) and body mass index (1.5 [1.9]; < 0.001). The most commonly observed adverse reactions were nausea (n = 9), in line with previous studies. Hypoglycemia events were rare; only reported in 2 patients.
Intensification strategy based on lixisenatide added to basal insulin (with or without oral antidiabetes drugs) can be an effective treatment option in patients with uncontrolled type 2 diabetes. In this small, selected population, glycemic control was significantly improved in terms of HbA1, fasting blood glucose levels, and postprandial glucose levels, with a reduction of body weight and low risk of hypoglycemic events. (. 2018; 79:XXX-XXX).
基础胰岛素可降低空腹血糖水平,但餐后血糖水平可能仍较高。传统的快速强化胰岛素治疗策略可能会导致低血糖发作和体重增加。胰高血糖素样肽-1受体激动剂,如短效的利司那肽,能够控制餐后血糖波动,不会导致体重增加,且低血糖事件风险较低。
由于在临床实践中利司那肽与基础胰岛素(联合或不联合口服抗糖尿病药物)联合使用的数据有限,本研究评估了强化治疗24周后与血糖控制相关参数及人体测量数据的变化。
这是一项对129例基础胰岛素治疗血糖控制不佳的2型糖尿病患者进行的多中心回顾性观察研究。在纳入研究前至少24周,通过加用利司那肽强化他们的治疗。回顾性收集数据以确定糖化血红蛋白(HbA1c)水平、血糖水平、体重和体重指数的变化。还记录了不良反应和低血糖事件。
在利司那肽强化治疗24周后,观察到HbA1c水平显著降低(-1.1%;<0.001)。30.2%的患者HbA1c<7%,17.1%的患者HbA1c<6.糖尿病及其并发症杂志5%。空腹血糖(31.8[60.3]mg/dL;<0.001)、餐后血糖(55.0[49]mg/dL;<0.001)水平、体重(4.0[5.4]kg;<0.001)和体重指数(1.5[1.9];<0.001)均有所降低。最常观察到的不良反应是恶心(n = 9),与既往研究一致。低血糖事件罕见;仅2例患者报告有低血糖事件。
在基础胰岛素(联合或不联合口服抗糖尿病药物)中加用利司那肽的强化治疗策略,对于血糖控制不佳的2型糖尿病患者可能是一种有效的治疗选择。在这个小规模的特定人群中,糖化血红蛋白、空腹血糖水平和餐后血糖水平方面的血糖控制得到显著改善,体重减轻,低血糖事件风险较低。(. 2018;79:XXX - XXX)