Unnikrishnan A G, Bantwal Ganapathi, Sahay R K
J Assoc Physicians India. 2014 Jan;62(1 Suppl):15-20.
There is a need for ideal basal insulin which can overcome the unmet need of a truly once daily insulin, with a flat peakless profile. Useful for all types of patients Insulin degludec is next generation insulin with a unique mode of protraction of forming soluble multi-hexamers and slow continuous absorption giving it a flat profile compared to the existing basal insulin. In patients with type 1 diabetes or with type 2 diabetes, at steady-state, the mean terminal half-life of insulin degludec was 25 hours, i.e., approximately twice as long as for insulin glargine (half-life of 12.1 hours). In once-daily dosing regimen it reaches steady state after approximately 3 days. The duration of action of insulin degludec was estimated to be beyond 42 hours in euglycaemic clamp studies and this gives the unique opportunity of flexible time dosing which is not an available option with the existing basal insulin. The glucose-lowering effect is evenly distributed across a 24-hour dosing interval with insulin degludec having 4 times lower variability than insulin glargine. This is an important attribute given the narrow therapeutic window of insulin and the goal of achieving night time and inter-prandial glycaemic control without increasing the risk for hypoglycaemia, a goal that is challenging given the variability of absorption and lower PK half-lives of current basal insulin products. The combination of the ultra-long, flat and stable profile with an improved hour-to-hour and day-to-day variability could present an improved risk-benefit trade-off with the lower risk of hypoglycaemia, allowing for targeting improved levels of glycaemic control.
需要一种理想的基础胰岛素,它能够满足真正每日一次、无峰浓度曲线的未被满足的需求。对所有类型的患者都有用 德谷胰岛素是新一代胰岛素,具有独特的延长作用模式,即形成可溶性多聚六聚体并缓慢持续吸收,与现有的基础胰岛素相比,它具有无峰浓度曲线。在1型糖尿病或2型糖尿病患者中,稳态时德谷胰岛素的平均终末半衰期为25小时,即大约是甘精胰岛素(半衰期为12.1小时)的两倍。在每日一次给药方案中,大约3天后达到稳态。在正常血糖钳夹研究中,德谷胰岛素的作用持续时间估计超过42小时,这提供了灵活定时给药的独特机会,而现有的基础胰岛素没有这种选择。德谷胰岛素的降糖作用在24小时给药间隔内均匀分布,其变异性比甘精胰岛素低4倍。鉴于胰岛素的治疗窗较窄,以及在不增加低血糖风险的情况下实现夜间和餐间血糖控制的目标,这是一个重要特性,鉴于目前基础胰岛素产品吸收的变异性和较低的药代动力学半衰期,这一目标具有挑战性。超长、无峰和稳定的曲线与改善的逐小时和逐日变异性相结合,可能会改善风险效益比,降低低血糖风险,从而实现更好的血糖控制水平。