Lower amounts of daily and prolonged sitting do not lower free-living continuously monitored glucose concentrations in overweight and obese adults: a randomised crossover study
Issue Date
2022-01-30Subjects
physical activitysedentary behaviour
postprandial glucose
blood glucose monitoring
overweight
obesity
Subject Categories::C600 Sports Science
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This study compared the short-term continuously monitored glucose responses between higher and lower amounts of prolonged sitting in overweight and obese adults under free-living conditions. In a randomised crossover design, 12 participants (age 48 ± 10 years, body mass index 33.3 ± 5.5 kg/m2 ) completed two four-day experimental regimens while wearing a continuous glucose monitor, as follows: (1) uninterrupted sitting (participants were instructed to sit for ≥10 h/day and accrue ≥7, 1 h sitting bouts each day), and (2) interrupted sitting (participants were instructed to interrupt sitting every 30 min during ten of their waking hours with 6–10 min of activity accrued in each hour). Linear mixed models compared outcomes between regimens. None of the continuously monitored glucose variables differed between regimens, e.g., 24 h net incremental area under the glucose curve was 5.9 [95% CI: −1.4, 13.1] and 5.6 [95% CI: −1.7, 12.8] mmol/L·24 h, respectively (p = 0.47). Daily sitting (−58 min/day, p = 0.001) and sitting bouts lasting ≥30 min (−99 min/day, p < 0.001) were significantly lower and stepping time significantly higher (+40 min/day, p < 0.001) in the interrupted sitting than the uninterrupted sitting regimen. In conclusion, lower amounts of daily and prolonged sitting did not improve free-living continuously measured glucose among overweight and obese adultsCitation
Bailey DP, Stringer CA, Maylor BD, Zakrzewski-Fruer JK (2022) 'Lower amounts of daily and prolonged sitting do not lower free-living continuously monitored glucose concentrations in overweight and obese adults: a randomised crossover study', Nutrients, 14 (3), pp.605-.Publisher
MDPIJournal
NutrientsPubMed ID
35276965PubMed Central ID
PMC8840170Additional Links
https://www.mdpi.com/2072-6643/14/3/605Type
ArticleLanguage
enISSN
2072-6643ae974a485f413a2113503eed53cd6c53
10.3390/nu14030605
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