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Model-Free Machine Learning in Biomedicine: Feasibility Study in Type 1 Diabetes

机译:生物医学中的无模型机器学习:1型糖尿病的可行性研究

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摘要

Although reinforcement learning (RL) is suitable for highly uncertain systems, the applicability of this class of algorithms to medical treatment may be limited by the patient variability which dictates individualised tuning for their usually multiple algorithmic parameters. This study explores the feasibility of RL in the framework of artificial pancreas development for type 1 diabetes (T1D). In this approach, an Actor-Critic (AC) learning algorithm is designed and developed for the optimisation of insulin infusion for personalised glucose regulation. AC optimises the daily basal insulin rate and insulin:carbohydrate ratio for each patient, on the basis of his/her measured glucose profile. Automatic, personalised tuning of AC is based on the estimation of information transfer (IT) from insulin to glucose signals. Insulin-to-glucose IT is linked to patient-specific characteristics related to total daily insulin needs and insulin sensitivity (SI). The AC algorithm is evaluated using an FDA-accepted T1D simulator on a large patient database under a complex meal protocol, meal uncertainty and diurnal SI variation. The results showed that 95.66% of time was spent in normoglycaemia in the presence of meal uncertainty and 93.02% when meal uncertainty and SI variation were simultaneously considered. The time spent in hypoglycaemia was 0.27% in both cases. The novel tuning method reduced the risk of severe hypoglycaemia, especially in patients with low SI.
机译:尽管强化学习(RL)适用于高度不确定的系统,但是此类算法在医学上的适用性可能会受到患者可变性的限制,而患者可变性要求针对其通常的多个算法参数进行个性化调整。这项研究探讨了在1型糖尿病(T1D)人工胰腺发育框架中RL的可行性。通过这种方法,设计并开发了Actor-Critic(AC)学习算法,用于针对个性化葡萄糖调节的胰岛素输注优化。 AC根据他/她测得的葡萄糖曲线,优化了每个患者的每日基础胰岛素率和胰岛素:碳水化合物比例。 AC的自动个性化调整基于对从胰岛素到葡萄糖信号的信息传递(IT)的估计。胰岛素-葡萄糖IT与特定于患者的特征有关,这些特征与每日总胰岛素需求和胰岛素敏感性(SI)有关。使用复杂的进餐方案,进餐不确定性和昼夜SI变化,使用FDA接受的T1D模拟器对大型患者数据库进行AC算法评估。结果表明,在有膳食不确定性的情况下,血糖正常的时间花费了95.66%,在同时考虑膳食不确定性和SI差异的情况下,花费了93.02%的时间。在两种情况下,花费在低血糖症上的时间为0.27%。新颖的调整方法降低了严重低血糖的风险,尤其是在SI较低的患者中。

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