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胰岛素耐量试验中胰岛素剂量优化计算方法:一项随机平行对照研究。

The Optimized Calculation Method for Insulin Dosage in an Insulin Tolerance Test (ITT): A Randomized Parallel Control Study.

机构信息

Department of Endocrine and Metabolic Diseases, Ruijin Hospital North, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

State Key Laboratory of Medical Genomics, National Clinical Research Center for Metabolic Diseases, Collaborative Innovation Center of Systems Biomedicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Front Endocrinol (Lausanne). 2020 Apr 9;11:202. doi: 10.3389/fendo.2020.00202. eCollection 2020.

Abstract

To explore the most suitable calculation method for insulin dosage in an insulin tolerance test (ITT) and to evaluate the clinical application value of the optimization coefficient (γ). In this study, 140 adult patients with congenital growth hormone deficiency (GHD) or acquired hypopituitarism were randomized into the following two groups: the conventional group ( = 70) and the optimized group ( = 70). Oral glucose tolerance tests (OGTTs), insulin release tests (IRTs), and ITTs were conducted. For ITTs, insulin doses were the product of body weight (kg) and related coefficient (0.15 IU/kg for the control group and γ IU/kg for the optimized group, respectively). Notably, γ was defined as -0.034 + 0.000176 × AUC + 0.009846 × BMI, which was based on our previous study. In the ITTs, the rate of achieving adequate hypoglycemia with a single insulin dose was significantly higher for the optimized group compared with the conventional group (92.9 vs. 60.0%, < 0.001). The optimized group required higher initial doses of insulin (0.23 IU/kg). Meanwhile, the two groups did not differ significantly in their nadir blood glucose (1.9 vs. 1.9 mmol/L, = 0.828). This study confirmed that the proposed optimized calculation method for insulin dosage in ITTs led to more efficient hypoglycemia achievement, without increasing the incidence of serious adverse events.

摘要

目的

探索胰岛素耐量试验(ITT)中胰岛素剂量计算的最适方法,并评估优化系数(γ)的临床应用价值。

方法

将 140 例成年先天性生长激素缺乏症(GHD)或获得性垂体功能减退症患者随机分为常规组(n=70)和优化组(n=70)。两组均进行口服葡萄糖耐量试验(OGTT)、胰岛素释放试验(IRT)和 ITT。ITT 中胰岛素剂量为体重(kg)与相关系数(对照组为 0.15 IU/kg,优化组为 γ IU/kg)的乘积。值得注意的是,γ定义为-0.034+0.000176×AUC+0.009846×BMI,该系数基于我们之前的研究。

结果

在 ITT 中,优化组单次胰岛素剂量达到充分低血糖的比例明显高于常规组(92.9% vs. 60.0%,<0.001)。优化组需要更高的初始胰岛素剂量(0.23 IU/kg)。同时,两组的血糖最低点无显著差异(1.9 vs. 1.9 mmol/L,=0.828)。

结论

本研究证实,ITT 中胰岛素剂量的优化计算方法可更有效地实现低血糖,且不增加严重不良事件的发生率。

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