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Severe Obstructive Sleep Apnea Disrupts Vigilance-State-Dependent Metabolism

The direct pathophysiological effects of obstructive sleep apnea (OSA) have been well described. However, the systemic and metabolic consequences of OSA are less well understood. The aim of this secondary analysis was to translate recent findings in healthy subjects on vigilance-state-dependent meta...

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Autores principales: Schmidt, Felix, Nowak, Nora, Baumgartner, Patrick, Gaisl, Thomas, Malesevic, Stefan, Streckenbach, Bettina, Sievi, Noriane A., Schwarz, Esther I., Zenobi, Renato, Brown, Steven A., Kohler, Malcolm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694615/
https://www.ncbi.nlm.nih.gov/pubmed/36430527
http://dx.doi.org/10.3390/ijms232214052
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author Schmidt, Felix
Nowak, Nora
Baumgartner, Patrick
Gaisl, Thomas
Malesevic, Stefan
Streckenbach, Bettina
Sievi, Noriane A.
Schwarz, Esther I.
Zenobi, Renato
Brown, Steven A.
Kohler, Malcolm
author_facet Schmidt, Felix
Nowak, Nora
Baumgartner, Patrick
Gaisl, Thomas
Malesevic, Stefan
Streckenbach, Bettina
Sievi, Noriane A.
Schwarz, Esther I.
Zenobi, Renato
Brown, Steven A.
Kohler, Malcolm
author_sort Schmidt, Felix
collection PubMed
description The direct pathophysiological effects of obstructive sleep apnea (OSA) have been well described. However, the systemic and metabolic consequences of OSA are less well understood. The aim of this secondary analysis was to translate recent findings in healthy subjects on vigilance-state-dependent metabolism into the context of OSA patients and answer the question of how symptomatic OSA influences metabolism and whether these changes might explain metabolic and cardiovascular consequences of OSA. Patients with suspected OSA were assigned according to their oxygen desaturation index (ODI) and Epworth Sleepiness Scale (ESS) score into symptomatic OSA and controls. Vigilance-state-dependent breath metabolites assessed by high-resolution mass spectrometry were used to test for a difference in both groups. In total, 44 patients were eligible, of whom 18 (40.9%) were assigned to the symptomatic OSA group. Symptomatic OSA patients with a median [25%, 75% quartiles] ODI of 40.5 [35.0, 58.8] events/h and an ESS of 14.0 [11.2, 15.8] showed moderate to strong evidence for differences in 18 vigilance-state-dependent breath compounds compared to controls. These identified metabolites are part of major metabolic pathways in carbohydrate, amino acid, and lipid metabolism. Thus, beyond hypoxia per se, we hypothesize that disturbed sleep in OSA patients persists as disturbed sleep-dependent metabolite levels during daytime.
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spelling pubmed-96946152022-11-26 Severe Obstructive Sleep Apnea Disrupts Vigilance-State-Dependent Metabolism Schmidt, Felix Nowak, Nora Baumgartner, Patrick Gaisl, Thomas Malesevic, Stefan Streckenbach, Bettina Sievi, Noriane A. Schwarz, Esther I. Zenobi, Renato Brown, Steven A. Kohler, Malcolm Int J Mol Sci Article The direct pathophysiological effects of obstructive sleep apnea (OSA) have been well described. However, the systemic and metabolic consequences of OSA are less well understood. The aim of this secondary analysis was to translate recent findings in healthy subjects on vigilance-state-dependent metabolism into the context of OSA patients and answer the question of how symptomatic OSA influences metabolism and whether these changes might explain metabolic and cardiovascular consequences of OSA. Patients with suspected OSA were assigned according to their oxygen desaturation index (ODI) and Epworth Sleepiness Scale (ESS) score into symptomatic OSA and controls. Vigilance-state-dependent breath metabolites assessed by high-resolution mass spectrometry were used to test for a difference in both groups. In total, 44 patients were eligible, of whom 18 (40.9%) were assigned to the symptomatic OSA group. Symptomatic OSA patients with a median [25%, 75% quartiles] ODI of 40.5 [35.0, 58.8] events/h and an ESS of 14.0 [11.2, 15.8] showed moderate to strong evidence for differences in 18 vigilance-state-dependent breath compounds compared to controls. These identified metabolites are part of major metabolic pathways in carbohydrate, amino acid, and lipid metabolism. Thus, beyond hypoxia per se, we hypothesize that disturbed sleep in OSA patients persists as disturbed sleep-dependent metabolite levels during daytime. MDPI 2022-11-14 /pmc/articles/PMC9694615/ /pubmed/36430527 http://dx.doi.org/10.3390/ijms232214052 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Schmidt, Felix
Nowak, Nora
Baumgartner, Patrick
Gaisl, Thomas
Malesevic, Stefan
Streckenbach, Bettina
Sievi, Noriane A.
Schwarz, Esther I.
Zenobi, Renato
Brown, Steven A.
Kohler, Malcolm
Severe Obstructive Sleep Apnea Disrupts Vigilance-State-Dependent Metabolism
title Severe Obstructive Sleep Apnea Disrupts Vigilance-State-Dependent Metabolism
title_full Severe Obstructive Sleep Apnea Disrupts Vigilance-State-Dependent Metabolism
title_fullStr Severe Obstructive Sleep Apnea Disrupts Vigilance-State-Dependent Metabolism
title_full_unstemmed Severe Obstructive Sleep Apnea Disrupts Vigilance-State-Dependent Metabolism
title_short Severe Obstructive Sleep Apnea Disrupts Vigilance-State-Dependent Metabolism
title_sort severe obstructive sleep apnea disrupts vigilance-state-dependent metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694615/
https://www.ncbi.nlm.nih.gov/pubmed/36430527
http://dx.doi.org/10.3390/ijms232214052
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