通过分析OpenAPS数据共享研究1型糖尿病的胰岛素需求

Isabella Degen, Kate Robson Brown, Zahraa S Abdallah
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 Objectives & ApproachOur research aims to improve the understanding of underexplored factors that drive changes in insulin needs of people with T1D. We use unsupervised time series pattern detection methods such as time series k-means, heatmaps and matrix profile to identify underexplored patterns. These are times when insulin on board (IOB) does not rise with more carbohydrates on board (COB) and times when BG does not fall with more IOB and/or rise with more COB as expected. In the future, we aim to use causal feature selection methods to exclude COB as a causal driver for these patterns and identify other factors as causal drivers.
 Relevance to Digital FootprintsWe use a digital footprints dataset of n=187 people who use an open-source automated insulin delivery system and have donated their data via the OpenAPS Data Commons and the OpenHumans.org platform. The data has been collected in real-life conditions and contains system logs, BG sensor data and various user-entered annotations. The richness of the data provides a unique opportunity to study what happens in real-life conditions but also poses challenges for many methods. These include inconsistencies between users, irregular sampling between devices and missing data.
 ResultsOur pattern detection methods can successfully identify underexplored patterns in insulin needs that are not directly driven by COB. These include months that require more/less insulin without eating more/less carbohydrates and times of day when blood glucose does not rise with more COB and/or fall with more IOB.
 Conclusions & ImplicationsWhile our current methods can identify underexplored patterns in insulin needs, the principal pattern identified remains the well-known pattern of the main meal COB spikes. This is not surprising given the frequency and impact of this pattern. We are working on methods that can identify both frequent and less frequent patterns as well as patterns arising from the irregularity of the sampling. Digital footprints datasets like the OpenAPS Data Commons are promising to help increase understanding of complex conditions such as T1D. More of this type of multi-year data is needed. Especially data that includes multiple different sensor readings to help identify causal drivers behind underexplored patterns of insulin needs. And we need pattern-finding methods that deal well with missing and irregularly sampled data.","PeriodicalId":132937,"journal":{"name":"International Journal for Population Data Science","volume":"170 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Studying insulin needs in Type 1 Diabetes by analysing the OpenAPS Data Commons\",\"authors\":\"Isabella Degen, Kate Robson Brown, Zahraa S Abdallah\",\"doi\":\"10.23889/ijpds.v8i3.2271\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction & BackgroundType 1 Diabetes (T1D) is a chronic condition where the body produces too little insulin, a hormone required to regulate blood glucose (BG). Finding the correct insulin dose and time remains a complex and as yet unsolved control task. Many factors such as food, exercise, stress, menstrual cycle, etc. change how much insulin is required. Most of these factors remain unobserved and/or underexplored. The NHS national diabetes audit shows that in 2020-21 only 9.8% of people with T1D had a NICE recommended glycated haemoglobin (HbA1c) test result of 48 mmol/mol or less to avoid complications due to diabetes.
 Objectives & ApproachOur research aims to improve the understanding of underexplored factors that drive changes in insulin needs of people with T1D. We use unsupervised time series pattern detection methods such as time series k-means, heatmaps and matrix profile to identify underexplored patterns. These are times when insulin on board (IOB) does not rise with more carbohydrates on board (COB) and times when BG does not fall with more IOB and/or rise with more COB as expected. In the future, we aim to use causal feature selection methods to exclude COB as a causal driver for these patterns and identify other factors as causal drivers.
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引用次数: 0

摘要

介绍,背景1型糖尿病(T1D)是一种慢性疾病,机体产生的胰岛素太少,而胰岛素是调节血糖(BG)所需的激素。找到正确的胰岛素剂量和时间仍然是一项复杂且尚未解决的控制任务。许多因素,如食物、运动、压力、月经周期等,都会改变胰岛素的需要量。这些因素中的大多数仍未被观察到和/或未被充分探索。NHS全国糖尿病审计显示,在2020- 2021年,只有9.8%的T1D患者的糖化血红蛋白(HbA1c)检测结果为NICE推荐的48 mmol/mol或更低,以避免糖尿病引起的并发症。目标,我们的研究旨在提高对驱动T1D患者胰岛素需求变化的未被探索因素的理解。我们使用无监督的时间序列模式检测方法,如时间序列k-means、热图和矩阵剖面来识别未被探索的模式。这些是胰岛素携带量(IOB)没有随着碳水化合物携带量(COB)的增加而升高的时间,以及BG没有像预期的那样随着碳水化合物携带量(COB)的增加而下降和/或升高的时间。在未来,我们的目标是使用因果特征选择方法来排除COB作为这些模式的因果驱动因素,并确定其他因素作为因果驱动因素。 与数字足迹相关我们使用n=187人的数字足迹数据集,这些人使用开源自动胰岛素输送系统,并通过OpenAPS数据共享和OpenHumans.org平台捐赠了他们的数据。这些数据是在实际情况下收集的,包括系统日志、BG传感器数据和各种用户输入的注释。丰富的数据为研究现实生活中发生的情况提供了独特的机会,但也对许多方法提出了挑战。这些问题包括用户之间的不一致,设备之间的不规则采样和数据丢失。 结果我们的模式检测方法可以成功地识别出胰岛素需求中未被探索的模式,这些模式不是由COB直接驱动的。这些包括需要更多/更少胰岛素而不吃更多/更少碳水化合物的月份,以及一天中血糖不随COB增加而上升和/或随IOB增加而下降的时间。结论,虽然我们目前的方法可以确定胰岛素需求中未被探索的模式,但确定的主要模式仍然是众所周知的主餐COB峰值模式。考虑到这种模式的频率和影响,这并不奇怪。我们正在研究能够识别频繁和不频繁的模式以及因采样不规律而产生的模式的方法。像OpenAPS数据共享这样的数字足迹数据集有望帮助增加对T1D等复杂情况的理解。需要更多这类多年数据。特别是数据包括多个不同的传感器读数,以帮助确定未被探索的胰岛素需求模式背后的因果驱动因素。我们还需要能够很好地处理缺失和不规则采样数据的模式查找方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studying insulin needs in Type 1 Diabetes by analysing the OpenAPS Data Commons
Introduction & BackgroundType 1 Diabetes (T1D) is a chronic condition where the body produces too little insulin, a hormone required to regulate blood glucose (BG). Finding the correct insulin dose and time remains a complex and as yet unsolved control task. Many factors such as food, exercise, stress, menstrual cycle, etc. change how much insulin is required. Most of these factors remain unobserved and/or underexplored. The NHS national diabetes audit shows that in 2020-21 only 9.8% of people with T1D had a NICE recommended glycated haemoglobin (HbA1c) test result of 48 mmol/mol or less to avoid complications due to diabetes. Objectives & ApproachOur research aims to improve the understanding of underexplored factors that drive changes in insulin needs of people with T1D. We use unsupervised time series pattern detection methods such as time series k-means, heatmaps and matrix profile to identify underexplored patterns. These are times when insulin on board (IOB) does not rise with more carbohydrates on board (COB) and times when BG does not fall with more IOB and/or rise with more COB as expected. In the future, we aim to use causal feature selection methods to exclude COB as a causal driver for these patterns and identify other factors as causal drivers. Relevance to Digital FootprintsWe use a digital footprints dataset of n=187 people who use an open-source automated insulin delivery system and have donated their data via the OpenAPS Data Commons and the OpenHumans.org platform. The data has been collected in real-life conditions and contains system logs, BG sensor data and various user-entered annotations. The richness of the data provides a unique opportunity to study what happens in real-life conditions but also poses challenges for many methods. These include inconsistencies between users, irregular sampling between devices and missing data. ResultsOur pattern detection methods can successfully identify underexplored patterns in insulin needs that are not directly driven by COB. These include months that require more/less insulin without eating more/less carbohydrates and times of day when blood glucose does not rise with more COB and/or fall with more IOB. Conclusions & ImplicationsWhile our current methods can identify underexplored patterns in insulin needs, the principal pattern identified remains the well-known pattern of the main meal COB spikes. This is not surprising given the frequency and impact of this pattern. We are working on methods that can identify both frequent and less frequent patterns as well as patterns arising from the irregularity of the sampling. Digital footprints datasets like the OpenAPS Data Commons are promising to help increase understanding of complex conditions such as T1D. More of this type of multi-year data is needed. Especially data that includes multiple different sensor readings to help identify causal drivers behind underexplored patterns of insulin needs. And we need pattern-finding methods that deal well with missing and irregularly sampled data.
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