Hildebrandt P R, Vaag A A
Hvidøre Hospital, Klampenborg, Denmark.
Diabetes Care. 1993 Jan;16(1):1-3. doi: 10.2337/diacare.16.1.1.
To determine the influence of local adiposity on insulin depot size during CSII at basal rate.
In 27 diabetic patients, a constant infusion of 125I-labeled Actrapid insulin was given, with U-40 insulin at a rate of 1.12 IU/h in 20 patients, and U-100 at a rate of 1 IU/h in 7 patients. After 16 h of infusion, the steady-state depot size was measured by external counting, and the local skin fold was measured with a Harpenden skin-fold caliper.
U-40 insulin infusion resulted in a steady-state depot size of 5.1 U (2.1-10.9 U), and a corresponding skin-fold thickness of 17.8 mm (5-34 mm). A positive correlation was found between depot size and skin-fold thickness. A similar correlation was observed with U-100 insulin.
During basal rate CSII, large variations in local skin-fold thickness create large variations in the steady-state depot size, which is partly predictable just by lifting the skin fold.
确定基础率持续皮下胰岛素输注(CSII)期间局部肥胖对胰岛素储存量的影响。
对27例糖尿病患者持续输注125I标记的中性胰岛素,20例患者以1.12 IU/h的速率输注U-40胰岛素,7例患者以1 IU/h的速率输注U-100胰岛素。输注16小时后,通过体外计数测量稳态储存量,并用哈彭德皮肤褶厚度仪测量局部皮肤褶厚度。
输注U-40胰岛素导致稳态储存量为5.1 U(2.1 - 10.9 U),相应的皮肤褶厚度为17.8 mm(5 - 34 mm)。储存量与皮肤褶厚度之间呈正相关。使用U-100胰岛素时也观察到类似的相关性。
在基础率CSII期间,局部皮肤褶厚度的巨大变化会导致稳态储存量的巨大变化,通过提起皮肤褶部分可预测这种变化。