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将理想基础胰岛素的结构转化为临床特性。

Translating structure to clinical properties of an ideal basal insulin.

作者信息

Unnikrishnan A G, Bantwal Ganapathi, Sahay R K

出版信息

J Assoc Physicians India. 2014 Jan;62(1 Suppl):15-20.

PMID:25330627
Abstract

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.

摘要

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。

相似文献

1
Translating structure to clinical properties of an ideal basal insulin.将理想基础胰岛素的结构转化为临床特性。
J Assoc Physicians India. 2014 Jan;62(1 Suppl):15-20.
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Basal insulin analogues in the management of diabetes mellitus: What progress have we made?基础胰岛素类似物在糖尿病治疗中的应用:我们取得了哪些进展?
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Degludec, a new ultra-long-acting basal insulin for the treatment of diabetes mellitus type 1 and 2: advances in clinical research.德谷胰岛素,一种用于治疗1型和2型糖尿病的新型超长效基础胰岛素:临床研究进展
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Variability of glucose-lowering effect as a limiting factor in optimizing basal insulin therapy: a review.降糖效果的变异性是优化基础胰岛素治疗的限制因素:综述。
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Morning administration of 0.4U/kg/day insulin glargine 300U/mL provides less fluctuating 24-hour pharmacodynamics and more even pharmacokinetic profiles compared with insulin degludec 100U/mL in type 1 diabetes.与 100U/mL 德谷胰岛素相比,1 型糖尿病患者每天接受 0.4U/kg 甘精胰岛素 300U/mL 治疗,其 24 小时药效动力学波动更小,药代动力学更平稳。
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引用本文的文献

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Comparison of Insulins Glargine and Degludec in Diabetic Rhesus Macaques () with CGM Devices.甘精胰岛素和德谷胰岛素在带 CGMS 设备的糖尿病恒河猴中的比较。
Comp Med. 2021 Jun 1;71(3):247-255. doi: 10.30802/AALAS-CM-20-000075. Epub 2021 May 25.
2
Differential Effect of Hypoalbuminemia on Hypoglycemia on Type 2 Diabetes Patients Treated with Insulin Glargine 300 U/ml and Insulin Degludec.低白蛋白血症对接受300 U/ml甘精胰岛素和德谷胰岛素治疗的2型糖尿病患者低血糖的不同影响。
Diabetes Ther. 2019 Aug;10(4):1535-1541. doi: 10.1007/s13300-019-0654-y. Epub 2019 Jun 21.
3
Insulin degludec/insulin aspart once daily in Type 2 diabetes: a comparison of simple or stepwise titration algorithms (BOOST : SIMPLE USE).
德谷胰岛素/门冬胰岛素每日一次治疗2型糖尿病:简单滴定算法与逐步滴定算法的比较(BOOST:简单使用)
Diabet Med. 2017 Feb;34(2):174-179. doi: 10.1111/dme.13069. Epub 2016 Mar 6.