Investigation of glucose fluctuations by approaches of multi-scale analysis

被引:0
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作者
Yunyun Lai
Zhengbo Zhang
Peiyao Li
Xiaoli Liu
YiXin Liu
Yi Xin
Weijun Gu
机构
[1] Beijing Institute of Technology,School of Life Science
[2] Chinese PLA General Hospital,Department of Biomedical Engineering
[3] Beijing University of Areonautics and Astronautics,School of Biological Science and Medical Engineering
[4] Human Centrifuge Medical Training Base of Chinese,Department of Endocrinology
[5] Air Force,undefined
[6] Chinese PLA General Hospital,undefined
关键词
Continuous glucose fluctuation; Multiple scales; Ensemble empirical mode decomposition; Refined composite multi-scale entropy; Mean absolute glycemic excursions;
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中图分类号
学科分类号
摘要
Glucose variability provides detailed information on glucose control and fluctuation. The aim of this study is to investigate the glucose variability by multi-scale analysis approach on 72-h glucose series captured by continuous glucose monitoring system (CGMS), gaining insights into the variability and complexity of the glucose time series data. Ninety-eight type 2 DM patients participated in this study, and 72-h glucose series from each subject were recorded by CGMS. Subjects were divided into two subgroups according to the mean amplitude of glycemic excursions (MAGE) value threshold at 3.9 based on Chinese standard. In this study, we applied two types of multiple scales analysis methods on glucose time series: ensemble empirical mode decomposition (EEMD) and refined composite multi-scale entropy (RCMSE). With EEMD, glucose series was decomposed into several intrinsic mode function (IMF), and glucose variability was examined on multiple time scales with periods ranging from 0.5 to 12 h. With RCMSE, complexity of the structure of glucose series was quantified at each time scale ranging from 5 to 30 min. Subgroup with higher MAGE value (>3.9) presented higher glycemic baseline and variability. There were significant differences in glycemic variability on IMFs3–5 between subgroups with MAGE>3.9 and MAGE < = 3.9 (p<0.001), but no significant differences in variability on IMFs1–2. The complexity of glucose series quantified by RCMSE showed statistically difference on each time scale from 5 to 30 min between subgroups (p<0.05). Glucose series from subjects with higher MAGE value represented higher variability but lower complexity on multiple time scales. Compared with traditional matrices measuring the glucose variability, approaches of EEMD and RCMSE can quantify the dynamic glycemic fluctuation in multiple time scales and provide us more detailed information on glycemic variability and complexity.
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页码:505 / 514
页数:9
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