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Update on Mathematical Modeling Research to Support the Development of Automated Insulin Delivery Systems

机译:支持自动胰岛素输送系统开发的数学模型研究的最新进展

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摘要

One year after its initial meeting, the Glycemia Modeling Working Group reconvened during the 2009 Diabetes Technology Meeting in San Francisco, CA. The discussion, involving 39 scientists, again focused on the need for individual investigators to have access to the clinical data required to develop and refine models of glucose metabolism, the need to understand the differences among the distinct models and control algorithms, and the significance of day-to-day subject variability. The key conclusion was that model-based comparisons of different control algorithms, or the models themselves, are limited by the inability to access individual model-patient parameters. It was widely agreed that these parameters, as opposed to the average parameters that are typically reported, are necessary to perform such comparisons. However, the prevailing view was that, if investigators were to make the parameters available, it would limit their ability (and that of their institution) to benefit from the invested work in developing their models. A general agreement was reached regarding the importance of each model having an insulin pharmacokinetic/pharmacodynamic profile that is not different from profiles reported in the literature (88% of the respondents agreed that the model should have similar curves or be analyzed separately) and the importance of capturing intraday variance in insulin sensitivity (91% of the respondents indicated that this could result in changes in fasting glucose of ≥15%, with 52% of the respondents believing that the variability could effect changes of ≥30%). Seventy-six percent of the participants indicated that high-fat meals were thought to effect changes in other model parameters in addition to gastric emptying. There was also widespread consensus as to how a closed-loop controller should respond to day-to-day changes in model parameters (with 76% of the participants indicating that fasting glucose should be within 15% of target, with 30% of the participants believing that it should be at target). The group was evenly divided as to whether the glucose sensor per se continues to be the major obstacle in achieving closed-loop control. Finally, virtually all participants agreed that a future two-day workshop should be organized to compare, contrast, and understand the differences among the different models and control algorithms.
机译:首次会议召开一年后,血糖模型研究工作组在2009年在加利福尼亚州旧金山举行的糖尿病技术会议上再次开会。涉及39位科学家的讨论再次着重于个人研究人员需要获得开发和完善葡萄糖代谢模型所需的临床数据,需要了解不同模型和控制算法之间的差异以及日常主题差异。关键结论是,不同控制算法或模型本身的基于模型的比较受到无法访问各个模型患者参数的限制。人们普遍认为,与通常报告的平均参数相反,这些参数是执行此类比较所必需的。但是,普遍的观点是,如果研究人员要提供参数,将会限制他们(及其机构)从开发模型中所投入的工作中受益的能力。对于每个模型的胰岛素药代动力学/药效学特征与文献中报道的特征没有什么不同(88%的受访者同意该模型应具有相似的曲线或分别进行分析)的重要性达成了普遍共识捕获胰岛素敏感性的日内差异(91%的受访者表示这可能导致空腹血糖变化≥15%,而52%的受访者认为这种变异性可能导致≥30%的变化)。 76%的参与者表示,高脂肪餐除了胃排空外,还影响其他模型参数的变化。关于闭环控制器应如何响应模型参数的日常变化也达成了广泛共识(76%的参与者表示空腹血糖应在目标的15%以内,其中30%的参与者认为应该达到目标)。关于血糖传感器本身是否继续继续成为实现闭环控制的主要障碍,该小组的意见是平均的。最后,几乎所有参与者都同意,应该组织一个为期两天的研讨会,以比较,对比和理解不同模型和控制算法之间的差异。

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