Cited by 10Sleep and related disordersSleep and Work-Related FatigueCircadian rhythm and melatonin

Modest sleep restriction does not influence steps, physical activity intensity or glucose tolerance in obese adults

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Porter, Jay W., Pettit‐Mee, Ryan J., Emerson, Travis S., McCrae, Christina S., Lastra, Guido, Vieira‐Potter, Victoria J., Parks, Elizabeth J., Kanaley, Jill A.·2021·Journal of Sleep Research

Abstract

Sleep restriction (SR) (<6 h) and physical activity (PA) are risk factors for obesity, but little work has examined the inter‐related influences of both risk factors. In a free‐living environment, 13 overweight/obese adults were sleep restricted for five nights to 6 h time‐in‐bed each night, with and without regular exercise (45 min/65% VO 2 max; counterbalanced design). Two days of recovery sleep followed SR. Subjects were measured during a mixed meal tolerance test (MMT), resting metabolic rate, cognitive testing and fat biopsy (n=8). SR increased peak glucose response (+7.3 mg/dl, p = .04), elevated fasting non‐esterified fatty acid (NEFA) concentrations (+0.1 mmol/L, p = .001) and enhanced fat oxidation (p < .001) without modifying step counts or PA intensity. Inclusion of daily exercise increased step count (+4,700 steps/day, p < .001) and decreased the insulin response to a meal (p = .01) but did not prevent the increased peak glucose response or elevated NEFA levels. The weekend recovery period improved fasting glucose (p = .02), insulin (p = .02), NEFA concentrations (p = .001) and HOMA‐IR (p < .01) despite reduced steps (p < .01) and increased sedentary time (p < .01). Abdominal adipose tissue (AT) samples, obtained after baseline, SR and exercise, did not differ in lipolytic capacity following SR. Fatty acid synthase protein content tended to increase following SR (p = .07), but not following exercise. In a free‐living setting, SR adversely affected circulating NEFAs, fuel oxidation and peak glucose response but did not directly affect glucose tolerance or AT lipolysis. SR‐associated metabolic impairments were not mitigated by exercise, yet recovery sleep completely rescued its adverse effects on glucose metabolism.

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Authors
Porter, J. W., Pettit‐Mee, R. J., Emerson, T. S., McCrae, C. S., Lastra, G., Vieira‐Potter, V. J., Parks, E. J., & Kanaley, J. A.
Affiliations
University of Missouri (US)
Corresponding author
Kanaley, Jill A.
Venue
Journal of Sleep Research
Publisher
Wiley
Published
2021-05-05
Volume
30
Issue
6
Pages
e13381-e13381
ISSN
  • 0962-1105 (ISSN-L)
  • 1365-2869
OpenAlex
W3158796827
Cited by
10
References
44
Citations by year
2026: 2 · 2025: 3 · 2024: 2 · 2023: 2 · 2022: 1
FWCI
1.21
Type
journal article
Language
en
Open access
Locations
  • Journal of Sleep Research (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institutes of Health (RO1 DK101513)
Topics
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
Keywords
sleep restriction, obesity, physical activity, glucose tolerance, insulin resistance, free fatty acids, fat oxidation, step count, sedentary behavior, abdominal fat, lipolysis, fatty acid synthase, recovery sleep, mixed meal tolerance test, resting metabolic rate
MeSH terms
Adult, Blood Glucose, Glucose, Humans, Insulin, Obesity, Sleep, Exercise

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