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Sleep Restriction for 1 Week Reduces Insulin Sensitivity in Healthy Men

OBJECTIVE: Short sleep duration is associated with impaired glucose tolerance and an increased risk of diabetes. The effects of sleep restriction on insulin sensitivity have not been established. This study tests the hypothesis that decreasing nighttime sleep duration reduces insulin sensitivity and...

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Autores principales: Buxton, Orfeu M., Pavlova, Milena, Reid, Emily W., Wang, Wei, Simonson, Donald C., Adler, Gail K.
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927933/
https://www.ncbi.nlm.nih.gov/pubmed/20585000
http://dx.doi.org/10.2337/db09-0699
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author Buxton, Orfeu M.
Pavlova, Milena
Reid, Emily W.
Wang, Wei
Simonson, Donald C.
Adler, Gail K.
author_facet Buxton, Orfeu M.
Pavlova, Milena
Reid, Emily W.
Wang, Wei
Simonson, Donald C.
Adler, Gail K.
author_sort Buxton, Orfeu M.
collection PubMed
description OBJECTIVE: Short sleep duration is associated with impaired glucose tolerance and an increased risk of diabetes. The effects of sleep restriction on insulin sensitivity have not been established. This study tests the hypothesis that decreasing nighttime sleep duration reduces insulin sensitivity and assesses the effects of a drug, modafinil, that increases alertness during wakefulness. RESEARCH DESIGN AND METHODS: This 12-day inpatient General Clinical Research Center study included 20 healthy men (age 20–35 years and BMI 20–30 kg/m(2)). Subjects spent 10 h/night in bed for ≥8 nights including three inpatient nights (sleep-replete condition), followed by 5 h/night in bed for 7 nights (sleep-restricted condition). Subjects received 300 mg/day modafinil or placebo during sleep restriction. Diet and activity were controlled. On the last 2 days of each condition, we assessed glucose metabolism by intravenous glucose tolerance test (IVGTT) and euglycemic-hyperinsulinemic clamp. Salivary cortisol, 24-h urinary catecholamines, and neurobehavioral performance were measured. RESULTS: IVGTT-derived insulin sensitivity was reduced by (means ± SD) 20 ± 24% after sleep restriction (P = 0.001), without significant alterations in the insulin secretory response. Similarly, insulin sensitivity assessed by clamp was reduced by 11 ± 5.5% (P < 0.04) after sleep restriction. Glucose tolerance and the disposition index were reduced by sleep restriction. These outcomes were not affected by modafinil treatment. Changes in insulin sensitivity did not correlate with changes in salivary cortisol (increase of 51 ± 8% with sleep restriction, P < 0.02), urinary catecholamines, or slow wave sleep. CONCLUSIONS: Sleep restriction (5 h/night) for 1 week significantly reduces insulin sensitivity, raising concerns about effects of chronic insufficient sleep on disease processes associated with insulin resistance.
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spelling pubmed-29279332011-09-01 Sleep Restriction for 1 Week Reduces Insulin Sensitivity in Healthy Men Buxton, Orfeu M. Pavlova, Milena Reid, Emily W. Wang, Wei Simonson, Donald C. Adler, Gail K. Diabetes Metabolism OBJECTIVE: Short sleep duration is associated with impaired glucose tolerance and an increased risk of diabetes. The effects of sleep restriction on insulin sensitivity have not been established. This study tests the hypothesis that decreasing nighttime sleep duration reduces insulin sensitivity and assesses the effects of a drug, modafinil, that increases alertness during wakefulness. RESEARCH DESIGN AND METHODS: This 12-day inpatient General Clinical Research Center study included 20 healthy men (age 20–35 years and BMI 20–30 kg/m(2)). Subjects spent 10 h/night in bed for ≥8 nights including three inpatient nights (sleep-replete condition), followed by 5 h/night in bed for 7 nights (sleep-restricted condition). Subjects received 300 mg/day modafinil or placebo during sleep restriction. Diet and activity were controlled. On the last 2 days of each condition, we assessed glucose metabolism by intravenous glucose tolerance test (IVGTT) and euglycemic-hyperinsulinemic clamp. Salivary cortisol, 24-h urinary catecholamines, and neurobehavioral performance were measured. RESULTS: IVGTT-derived insulin sensitivity was reduced by (means ± SD) 20 ± 24% after sleep restriction (P = 0.001), without significant alterations in the insulin secretory response. Similarly, insulin sensitivity assessed by clamp was reduced by 11 ± 5.5% (P < 0.04) after sleep restriction. Glucose tolerance and the disposition index were reduced by sleep restriction. These outcomes were not affected by modafinil treatment. Changes in insulin sensitivity did not correlate with changes in salivary cortisol (increase of 51 ± 8% with sleep restriction, P < 0.02), urinary catecholamines, or slow wave sleep. CONCLUSIONS: Sleep restriction (5 h/night) for 1 week significantly reduces insulin sensitivity, raising concerns about effects of chronic insufficient sleep on disease processes associated with insulin resistance. American Diabetes Association 2010-09 2010-06-28 /pmc/articles/PMC2927933/ /pubmed/20585000 http://dx.doi.org/10.2337/db09-0699 Text en © 2010 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Metabolism
Buxton, Orfeu M.
Pavlova, Milena
Reid, Emily W.
Wang, Wei
Simonson, Donald C.
Adler, Gail K.
Sleep Restriction for 1 Week Reduces Insulin Sensitivity in Healthy Men
title Sleep Restriction for 1 Week Reduces Insulin Sensitivity in Healthy Men
title_full Sleep Restriction for 1 Week Reduces Insulin Sensitivity in Healthy Men
title_fullStr Sleep Restriction for 1 Week Reduces Insulin Sensitivity in Healthy Men
title_full_unstemmed Sleep Restriction for 1 Week Reduces Insulin Sensitivity in Healthy Men
title_short Sleep Restriction for 1 Week Reduces Insulin Sensitivity in Healthy Men
title_sort sleep restriction for 1 week reduces insulin sensitivity in healthy men
topic Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927933/
https://www.ncbi.nlm.nih.gov/pubmed/20585000
http://dx.doi.org/10.2337/db09-0699
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