Impact of free-living pattern of sedentary behaviour on intra-day glucose regulation in type 2 diabetes

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Paing, Aye C. and McMillan, Kathryn A. and Kirk, Alison F. and Collier, Andrew and Hewitt, Allan and Chastin, Sebastien F.M. (2020) Impact of free-living pattern of sedentary behaviour on intra-day glucose regulation in type 2 diabetes. European Journal of Applied Physiology, 120. pp. 171-179. ISSN 1439-6327 (https://doi.org/10.1007/s00421-019-04261-z)

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Abstract

Purpose: To investigate how the pattern of sedentary behaviour affects intra-day glucose regulation in type 2 diabetes. Methods: This intensive longitudinal study was conducted in 37 participants with type 2 diabetes (age, 62.8 ± 10.5 years). Glucose and sedentary behaviour/physical activity were assessed with a continuous glucose monitoring (Abbott FreeStyle Libre) and an activity monitor (activPAL3) for 14 days. Multiple regression models with generalised estimating equations (GEEs) approach were used to assess the associations of sedentary time and breaks in sedentary time with pre-breakfast glucose, pre-lunch glucose, pre-dinner glucose, post-breakfast glucose, post-lunch glucose, post-dinner glucose, bedtime glucose, the dawn phenomenon, time in target glucose range (TIR, glucose 3.9–10 mmol/L) and time above target glucose range (TAR, glucose > 10 mmol/L). Results: Sedentary time was associated with higher pre-breakfast glucose (p = 0.001), pre-dinner glucose (p < 0.001), post-lunch glucose (p = 0.005), post-dinner glucose (p = 0.013) and the dawn phenomenon (p < 0.001). Breaks in sedentary time were associated with lower pre-breakfast glucose (p = 0.023), pre-dinner glucose (p = 0.023), post-breakfast glucose (p < 0.001) and the dawn phenomenon (p = 0.004). The association between sedentary time and less TIR (p = 0.022) and the association between breaks in sedentary time and more TIR (p = 0.001) were also observed. Conclusions: Reducing sedentary time and promoting breaks in sedentary time could be clinically relevant to improve intra-day glucose regulation in type 2 diabetes.

ORCID iDs

Paing, Aye C., McMillan, Kathryn A. ORCID logoORCID: https://orcid.org/0000-0001-5849-9666, Kirk, Alison F. ORCID logoORCID: https://orcid.org/0000-0002-6534-3763, Collier, Andrew, Hewitt, Allan ORCID logoORCID: https://orcid.org/0000-0002-5688-5069 and Chastin, Sebastien F.M.;
CORE (COnnecting REpositories)