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No Impaired Glucose Tolerance in Primary Insomnia Patients with Normal Results of Polysomnography
BACKGROUND: According to recent studies, sleep restriction and disruption both have a prominent negative influence on glucose metabolism. This could also be shown in sleep disorders, such as sleep apnea and the restless legs syndrome. However, similar studies regarding insomnia have not been that co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484770/ https://www.ncbi.nlm.nih.gov/pubmed/28701993 http://dx.doi.org/10.3389/fneur.2017.00303 |
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author | Tschepp, Johanna Lauer, Christoph J. Wilde-Frenz, Johanna Pollmächer, Thomas |
author_facet | Tschepp, Johanna Lauer, Christoph J. Wilde-Frenz, Johanna Pollmächer, Thomas |
author_sort | Tschepp, Johanna |
collection | PubMed |
description | BACKGROUND: According to recent studies, sleep restriction and disruption both have a prominent negative influence on glucose metabolism. This could also be shown in sleep disorders, such as sleep apnea and the restless legs syndrome. However, similar studies regarding insomnia have not been that consistent, yet. Moreover, most previous studies did not include objective polysomnography (PSG) data. METHODS: Patients with primary insomnia (N = 17) and healthy controls (N = 15) were investigated using psychometric tests such as the Epworth Sleepiness Scale and the Pittsburgh sleep quality index (PSQI). Two nights of full PSG were performed in all subjects, and after the first PSG night subjects underwent a standard oral glucose tolerance test (OGTT). PSG-, arousal-, and glucose metabolism-parameters were compared between groups. RESULTS: Patients with insomnia were, as expected, sleepier than healthy controls and showed higher PSQI values. All PSG parameters, however, including parameters related to nocturnal arousals, did not differ between groups. Moreover, OGGT results and all other parameters of glucose tolerance were not different between insomniac patients and healthy controls. CONCLUSION: Our findings suggest that glucose tolerance is not impaired in patients with chronic insomnia and normal PSG-findings. Therefore, impaired glucose metabolism and diabetes related to insomnia in earlier studies might be restricted to those patients who have objectively disturbed sleep. |
format | Online Article Text |
id | pubmed-5484770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54847702017-07-12 No Impaired Glucose Tolerance in Primary Insomnia Patients with Normal Results of Polysomnography Tschepp, Johanna Lauer, Christoph J. Wilde-Frenz, Johanna Pollmächer, Thomas Front Neurol Neuroscience BACKGROUND: According to recent studies, sleep restriction and disruption both have a prominent negative influence on glucose metabolism. This could also be shown in sleep disorders, such as sleep apnea and the restless legs syndrome. However, similar studies regarding insomnia have not been that consistent, yet. Moreover, most previous studies did not include objective polysomnography (PSG) data. METHODS: Patients with primary insomnia (N = 17) and healthy controls (N = 15) were investigated using psychometric tests such as the Epworth Sleepiness Scale and the Pittsburgh sleep quality index (PSQI). Two nights of full PSG were performed in all subjects, and after the first PSG night subjects underwent a standard oral glucose tolerance test (OGTT). PSG-, arousal-, and glucose metabolism-parameters were compared between groups. RESULTS: Patients with insomnia were, as expected, sleepier than healthy controls and showed higher PSQI values. All PSG parameters, however, including parameters related to nocturnal arousals, did not differ between groups. Moreover, OGGT results and all other parameters of glucose tolerance were not different between insomniac patients and healthy controls. CONCLUSION: Our findings suggest that glucose tolerance is not impaired in patients with chronic insomnia and normal PSG-findings. Therefore, impaired glucose metabolism and diabetes related to insomnia in earlier studies might be restricted to those patients who have objectively disturbed sleep. Frontiers Media S.A. 2017-06-27 /pmc/articles/PMC5484770/ /pubmed/28701993 http://dx.doi.org/10.3389/fneur.2017.00303 Text en Copyright © 2017 Tschepp, Lauer, Wilde-Frenz and Pollmächer. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Tschepp, Johanna Lauer, Christoph J. Wilde-Frenz, Johanna Pollmächer, Thomas No Impaired Glucose Tolerance in Primary Insomnia Patients with Normal Results of Polysomnography |
title | No Impaired Glucose Tolerance in Primary Insomnia Patients with Normal Results of Polysomnography |
title_full | No Impaired Glucose Tolerance in Primary Insomnia Patients with Normal Results of Polysomnography |
title_fullStr | No Impaired Glucose Tolerance in Primary Insomnia Patients with Normal Results of Polysomnography |
title_full_unstemmed | No Impaired Glucose Tolerance in Primary Insomnia Patients with Normal Results of Polysomnography |
title_short | No Impaired Glucose Tolerance in Primary Insomnia Patients with Normal Results of Polysomnography |
title_sort | no impaired glucose tolerance in primary insomnia patients with normal results of polysomnography |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484770/ https://www.ncbi.nlm.nih.gov/pubmed/28701993 http://dx.doi.org/10.3389/fneur.2017.00303 |
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