Hegab Ahmed M
Department of Pediatrics, Faculty of Medicine, Sohag University, Sohag, Egypt.
Front Pediatr. 2022 Mar 8;10:854972. doi: 10.3389/fped.2022.854972. eCollection 2022.
Estimation of insulin sensitivity factor (ISF) is essential for correction insulin doses calculation. This study aimed to assess real-life ISF among children and adolescents with type 1 diabetes using ultra-long-acting basal insulin analogs and to detect factors associated with ISF among those patients.
This prospective observational study was conducted at Sohag University Hospital, Egypt, and included 93 participants aged 6-18 years, diagnosed with T1DM for at least 1 year and using insulin glargine 300 Units/mL or insulin degludec 100 Units/mL as basal insulin. The ISF, insulin-to-carbohydrate ratio (ICR) and insulin doses were initially assessed then adjusted as required. The participants were regularly contacted throughout the follow-up period. Glycemic control parameters were assessed after 3 months.
The ISF showed diurnal variation with higher correction dose requirements for the morning than for the rest of the day ( < 0.001). This pattern of diurnal variation was found in participants with different pubertal stages and in participants using either type of ultra-long acting basal insulin analogs. There was no significant difference between the ISF calculated according to the 1800 rule [1800/Total daily insulin dose (TDD)] and the morning ISF ( = 0.25). The 1800 rule-calculated ISF was significantly lower than the actual ISF for the afternoon ( < 0.001) and the evening ( < 0.001). ISF at different times of the day were significantly correlated with age, body mass index, pubertal stage, diabetes duration, TDD, and ICR. Multiple regression analysis revealed that ICR was the most significant factor associated with ISF. Linear regression analysis revealed that the ISF (in mg/dL) for any time of the day could be estimated as 5.14 × ICR for the same time of the day (coefficient = 5.14, 95% confidence interval: 5.10-5.19, = 0.95, < 0.001).
Diurnal variation of ISF that had to be considered for proper calculation of correction doses. This diurnal variation was found in children and adolescents with different pubertal stages. The 1800 rule was appropriate for the morning correction doses but not in the afternoon or the evening. The TDD and the ICR could be used for ISF estimation.
胰岛素敏感因子(ISF)的估算对于校正胰岛素剂量的计算至关重要。本研究旨在评估使用超长效基础胰岛素类似物的1型糖尿病儿童和青少年的实际ISF,并检测这些患者中与ISF相关的因素。
这项前瞻性观察性研究在埃及索哈杰大学医院进行,纳入了93名年龄在6至18岁之间的参与者,他们被诊断为T1DM至少1年,且使用甘精胰岛素300单位/毫升或德谷胰岛素100单位/毫升作为基础胰岛素。最初评估ISF、胰岛素与碳水化合物比值(ICR)和胰岛素剂量,然后根据需要进行调整。在整个随访期间定期联系参与者。3个月后评估血糖控制参数。
ISF呈现昼夜变化,早晨的校正剂量需求高于一天中的其他时间(<0.001)。这种昼夜变化模式在不同青春期阶段的参与者以及使用任何一种超长效基础胰岛素类似物的参与者中均有发现。根据1800法则[1800/每日总胰岛素剂量(TDD)]计算的ISF与早晨的ISF之间无显著差异(=0.25)。根据1800法则计算的ISF在下午(<0.001)和晚上(<0.001)显著低于实际ISF。一天中不同时间的ISF与年龄、体重指数、青春期阶段、糖尿病病程、TDD和ICR显著相关。多元回归分析显示,ICR是与ISF相关的最显著因素。线性回归分析显示,一天中任何时间的ISF(以mg/dL为单位)可估计为同一时间的5.(此处原文似乎有误,应是5.14)×ICR(系数=5.14,95%置信区间:5.10 - 5.19,=0.95,<0.001)。
在正确计算校正剂量时必须考虑ISF的昼夜变化。这种昼夜变化在不同青春期阶段的儿童和青少年中均有发现。1800法则适用于早晨的校正剂量,但不适用于下午或晚上。TDD和ICR可用于ISF的估算。