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arXiv 2405.08970q-bio.QM
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使用开源自动胰岛素输送系统的个体中,低血糖对随时间变化的葡萄糖变异性的影响

Impact of Hypoglycemia on Glucose Variability Over Time for Individuals with Open Source Automated Insulin Delivery Systems

Arsalan Shahid, Dana M. Lewis

AI总结:

本研究基于122名使用开源AID系统的1型糖尿病患者的CGM数据,发现低血糖(尤其是严重低血糖)会显著延长后续血糖变异性的恢复时间,且存在低血糖循环发生与血糖反弹模式,为AID算法优化和糖尿病健康教育提供了参考。

摘要:

研究背景:本研究调查了使用开源自动胰岛素输送(automated insulin delivery, AID)系统的1型糖尿病患者在不同程度低血糖发生前后的葡萄糖状态,同时旨在评估低血糖与后续血糖变异性之间的关联。\n研究方法:研究分析了来自OpenAPS Data Commons(OpenAPS数据共享库)的122名使用开源AID系统的1型糖尿病患者的连续血糖监测(continuous glucose monitor, CGM)数据,全面分析了低血糖对血糖变异性的影响,覆盖低血糖发生前后的多个时间段。\n研究结果:低血糖后血糖变异性恢复正常最长需要48小时,其中严重低血糖(血糖值40-50 mg/dL)与更长的正常化时长相关。研究观察到一种循环模式:即使使用AID系统,低血糖也会使个体更易发生后续低血糖。低血糖发生前通常会出现血糖水平升高,严重低血糖后则会出现高于目标范围时间(time above range, TAR)均值升高的情况,表明存在“反弹”效应。不同的低血糖分类方法在血糖变异性结果上未表现出显著差异,但低血糖的程度确实会影响后续血糖波动的模式。\n研究结论:即使使用AID系统,低血糖(尤其是程度更低的严重低血糖)仍会显著影响后续的血糖变异性。这一结论需要在更广泛的商用AID系统中开展进一步研究,以确认这些模式是否适用于所有类型的AID系统。如果这些模式在所有类型的AID系统中都存在,将凸显出AID算法的潜在优化空间,同时也强调了向医疗服务提供者和糖尿病患者普及低血糖后血糖变异性相关知识的重要性。

英文摘要:

Background: This study investigates glucose conditions preceding and following various hypoglycemia levels in individuals with type 1 diabetes using open-source automated insulin delivery (AID) systems. It also seeks to evaluate relationships between hypoglycemia and subsequent glycemic variability. Methods: Analysis of continuous glucose monitor (CGM) data from 122 individuals with type 1 diabetes using open-source AID from the OpenAPS Data Commons was conducted. The study comprehensively analyzed the effects of hypoglycemia on glycemic variability, covering time periods before and after hypoglycemia. Results: Glucose variability normalization post-hypoglycemia can take up to 48 hours, with severe hypoglycemia (40-50 mg/dL) linked to prolonged normalization. A cyclical pattern was observed where hypoglycemia predisposes individuals to further hypoglycemia, even with AID system use. A rise in glucose levels often precedes hypoglycemia, followed by an elevated mean time above range (TAR) post-severe hypoglycemia, indicating a 'rebound' effect. Different hypoglycemia categorization approaches did not show significant differences in glycemic variability outcomes. The level of hypoglycemia does influence the pattern of subsequent glucose fluctuations. Conclusion: Hypoglycemia, especially at lower levels, significantly impact subsequent glycemic variability, even with use of AID systems. This should be studied further with a broader set of commercial AID systems to understand if these patterns are true of all types of AID systems. If these patterns occur in all types of AID systems, it underscores potential opportunities for enhancements in AID algorithms and highlights the importance of educating healthcare providers and people with diabetes about post-hypoglycemia glucose variability.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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