1 Department of Psychiatry and Neurobehavioral Sciences, Department of Medicine, University of Virginia , Charlottesville, Virginia.
Diabetes Technol Ther. 2013 Nov;15(11):935-41. doi: 10.1089/dia.2013.0150. Epub 2013 Aug 26.
Insulin-induced hypoglycemia is as a critical barrier in the treatment of type 1 diabetes mellitus patients and may lead to unconsciousness, brain damage, or even death. Clinically, glucagon is used as a rescue drug to treat severe hypoglycemic episodes. More recently, in a bihormonal closed-loop glucose control, glucagon has been used subcutaneously along with insulin for protection against hypoglycemia. In this context, small doses of glucagon are frequently administered. The efficacy and safety of such systems, however, require precise information on the pharmacokinetics of the glucagon transport from the administrative site to the circulation, which is currently lacking. The goal of this work is to address this need by developing and validating a mathematical model of exogenous glucagon transport to the plasma.
Eight pharmacokinetic models with various levels of complexity were fitted to nine clinical datasets. An optimal model was chosen in two consecutive steps. At Step 1, all models were screened for parameter identifiability (discarding the unidentifiable candidates). At Step 2, the remaining models are compared based on Bayesian information criterion.
At Step 1, two models were removed for higher parameter fractional SDs. Another three were discarded for location of their optimal parameters on the parameter search boundaries. At Step 2, an optimal model was selected based on the Bayesian information criterion. It has a simple linear structure, assuming that glucagon is injected into one compartment, from where it enters a pool for a slower release into a third, plasma compartment. In the first and third compartments, glucagon is cleared at a rate proportional to its concentration.
A linear kinetic model of glucagon intervention has been developed and validated. It is expected to provide guidance for glucagon delivery and the construction of preclinical simulation testing platforms.
胰岛素诱导的低血糖是 1 型糖尿病治疗的一个关键障碍,可能导致昏迷、脑损伤甚至死亡。临床上,胰高血糖素被用作治疗严重低血糖发作的抢救药物。最近,在双激素闭环血糖控制中,胰高血糖素与胰岛素一起皮下给药,以防止低血糖。在这种情况下,经常给予小剂量的胰高血糖素。然而,这些系统的疗效和安全性需要精确的信息,了解从给药部位到循环系统的胰高血糖素转运的药代动力学,目前这方面的信息还缺乏。这项工作的目的是通过开发和验证外源性胰高血糖素向血浆转运的数学模型来满足这一需求。
用 8 种不同复杂程度的药代动力学模型拟合了 9 个临床数据集。通过连续两步选择最优模型。在第 1 步中,筛选所有模型的参数可识别性(排除不可识别的候选模型)。在第 2 步中,根据贝叶斯信息准则比较剩余模型。
在第 1 步中,有两个模型因参数的分数标准差较高而被剔除。另外三个模型因最优参数位于参数搜索边界上而被剔除。在第 2 步中,根据贝叶斯信息准则选择了一个最优模型。它具有简单的线性结构,假设胰高血糖素被注入一个隔室,从那里它进入一个较慢释放到第三个隔室的池,即血浆隔室。在第一和第三隔室中,胰高血糖素的清除速度与其浓度成正比。
已经开发和验证了胰高血糖素干预的线性动力学模型。预计它将为胰高血糖素输送和临床前模拟测试平台的构建提供指导。