Key result
Lower MAGE is linked to decreased complexity of continuous glucose time series versus high MAGE.
Why the study?
The complexity of glucose fluctuation and its relationship with glucose homeostasis regulation in type II diabetes mellitus require improved analytical methods for better understanding.
Does the complexity of glucose dynamics measured by RCMSE correlate with MAGE and HbA1c in patients with type II diabetes mellitus?
Observational (n=93)
Does the complexity of glucose dynamics measured by RCMSE correlate with MAGE and HbA1c in patients with type II diabetes mellitus?
RCMSE analysis of continuous glucose monitoring data reveals that reduced complexity of glucose dynamics indicates impaired gluco-regulation, offering a potential new biomarker for glucose fluctuation.
May refine glycemic regulation insights in T2DM; extends multi-scale entropy methodology but leaves clinical utility open.
The study on complexity of glucose fluctuation not only helps us understand the regulation of the glucose homeostasis system but also brings us a new insight of the research methodology on glucose regulation. In the experiments, we analyzed the complexity of the temporal structure of the 72 hours continuous glucose time series from a group of 93 subjects with type Ⅱ diabetes mellitus using the multi-scale entropy method. We adapted the most recently improved refined composite multi-scale entropy(RCMSE) algorithm which could overcome the shortcomings on the 72 hours short time series analysis. We then quantified and compared the complexity of continuous glucose time series between groups with type Ⅱ diabetes mellitus with different mean absolute glycemic excursion(MAGE) and glycated hemoglobin(Hb A1c). The results implied that the complexity of glucose time series decreased on lower MAGE group compared to high MAGE group, and the entropy on scale 1 to 6 which corresponded to 5 to 30 min had significant differences between these two groups; the complexity of glucose time series decreased with the increasing Hb A1 c level but the entropy had no statistical difference among groups at different scales. Therefore, RCMSE provided us with a new prospect to analyze the glucose time series and it was proved that less complexity of glucose dynamics could indicate the impaired gluco-regulation function from the MAGE point of view or Hb A1 c for patients, and the glucose complexity had the potential to become a new biomarker to reflect the fluctuation of the glucose time series.
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Lai et al. (2017) conducted an observational in Type II diabetes mellitus (n=93). Mean absolute glycemic excursion (MAGE) and HbA1c levels vs. Different MAGE and HbA1c groups was evaluated on Complexity of continuous glucose time series measured by refined composite multi-scale entropy. Lower mean absolute glycemic excursion was associated with decreased complexity of glucose time series compared to high MAGE, with significant differences on entropy scales 1 to 6 (5 to 30 min).
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