Morales Javier
Advanced Internal Medicine Group, New Hyde Park, New York 11042, USA.
Drugs. 2007;67(17):2557-84. doi: 10.2165/00003495-200767170-00007.
Insulin detemir is a novel long-acting insulin analogue with a unique mechanism underlying its prolonged duration of action. Unlike neutral protamine Hagedorn (NPH) insulin (insulin suspension isophane) and insulin glargine, which precipitate after administration, insulin detemir remains soluble after it is injected. The prolonged duration of action of insulin detemir is a result of the ability to self-associate into hexamers and dihexamers, and to bind reversibly to albumin. This mechanism of protraction provides a more prolonged, consistent and predictable glycaemic effect in patients with type 1 or type 2 diabetes mellitus compared with NPH insulin. Clinical studies have demonstrated that insulin detemir administered once or twice daily is at least as effective as NPH insulin and insulin glargine in achieving glycaemic control. Most trials have also shown that insulin detemir exhibits less intrapatient variability in glycaemic control compared with NPH insulin and insulin glargine. One of the benefits of insulin detemir is its favourable effect on bodyweight. Insulin detemir has shown weight neutrality in patients with type 1 diabetes and is associated with less weight gain than NPH insulin in clinical studies. Patients with type 2 diabetes using insulin detemir gain less weight than patients using NPH insulin and insulin glargine. In addition, a reduced risk of hypoglycaemia, particularly nocturnal hypoglycaemia, has been reported with insulin detemir compared with NPH insulin in patients with type 1 and type 2 diabetes. A reduced risk of major and nocturnal hypoglycaemia compared with insulin glargine in patients with type 1 diabetes has also been observed. Together, these data indicate that insulin detemir is a valuable new option for basal insulin therapy in patients with type 1 or type 2 diabetes.
地特胰岛素是一种新型长效胰岛素类似物,其作用持续时间延长的机制独特。与中性鱼精蛋白锌胰岛素(NPH胰岛素,即低精蛋白胰岛素混悬液)和甘精胰岛素不同,NPH胰岛素和甘精胰岛素给药后会沉淀,而地特胰岛素注射后仍保持可溶状态。地特胰岛素作用持续时间延长是其能够自缔合成六聚体和双六聚体,并与白蛋白可逆性结合的结果。与NPH胰岛素相比,这种延长作用机制为1型或2型糖尿病患者提供了更持久、稳定且可预测的血糖控制效果。临床研究表明,每日注射一次或两次地特胰岛素在实现血糖控制方面至少与NPH胰岛素和甘精胰岛素一样有效。大多数试验还表明,与NPH胰岛素和甘精胰岛素相比,地特胰岛素在患者体内血糖控制的变异性更小。地特胰岛素的一个优点是对体重有有利影响。在1型糖尿病患者中,地特胰岛素已显示出体重中性,并且在临床研究中与比NPH胰岛素更少的体重增加相关。使用地特胰岛素的2型糖尿病患者比使用NPH胰岛素和甘精胰岛素的患者体重增加更少。此外,与NPH胰岛素相比,1型和2型糖尿病患者使用地特胰岛素后低血糖风险降低,尤其是夜间低血糖风险。在1型糖尿病患者中,与甘精胰岛素相比,地特胰岛素的严重和夜间低血糖风险也有所降低。总之,这些数据表明,地特胰岛素是1型或2型糖尿病患者基础胰岛素治疗的一个有价值的新选择。