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Investigation of Urinary Sestrin2 in Patients with Obstructive Sleep Apnea

BACKGROUND: Obstructive sleep apnea (OSA) is a disease seriously threatening individual health, which results in serious complications such as hypertension and stroke. These complications are associated with oxidative stress triggered by intermittent hypoxia in OSA. Sestrin2 is a crucial factor invo...

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Autores principales: Bai, Lu, Sun, Chunying, Zhai, Huifen, Chen, Chen, Hu, Xiaotian, Ye, Xiulin, Li, Min, Fang, Yan, Yang, Weimin, Wang, Haoyan, Sun, Shibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486896/
https://www.ncbi.nlm.nih.gov/pubmed/30770985
http://dx.doi.org/10.1007/s00408-019-00205-8
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author Bai, Lu
Sun, Chunying
Zhai, Huifen
Chen, Chen
Hu, Xiaotian
Ye, Xiulin
Li, Min
Fang, Yan
Yang, Weimin
Wang, Haoyan
Sun, Shibo
author_facet Bai, Lu
Sun, Chunying
Zhai, Huifen
Chen, Chen
Hu, Xiaotian
Ye, Xiulin
Li, Min
Fang, Yan
Yang, Weimin
Wang, Haoyan
Sun, Shibo
author_sort Bai, Lu
collection PubMed
description BACKGROUND: Obstructive sleep apnea (OSA) is a disease seriously threatening individual health, which results in serious complications such as hypertension and stroke. These complications are associated with oxidative stress triggered by intermittent hypoxia in OSA. Sestrin2 is a crucial factor involved in oxidative stress. The goal of this study was to investigate if a relationship exists between OSA and Sestrin2. METHODS: We prospectively enrolled 71 subjects, and 16 patients of them with severe OSA completed 4 weeks of nasal continuous positive airway pressure (nCPAP) therapy. We measured and compared the concentration of Sestrin2 in the urine of all subjects, as well as the changes between before and after nCPAP treatment. Additionally, the correlation between Sestrin2 and sleep parameters was analyzed, and the multiple linear regression analysis with stepwise selection was performed to explore the relationship between Sestrin2 and various factors. RESULTS: A total of 71 subjects were enrolled and divided into two groups: OSA group (n = 41), control group (n = 30). The level of urinary Sestrin2 in OSA patients was significantly higher than that of the control group, and increased with the severity of OSA, while it reduced after nCPAP treatment. Additionally, Sestrin2 was positively correlated with apnea/hypopnea index (AHI), oxygen desaturation index, oxygen saturation < 90% percentage of recording time spent (PRTS) and high-density lipoprotein (HDL), while negatively correlated with the lowest oxygen saturation. Importantly, Sestrin2 was independently associated with AHI, oxygen saturation < 90% PRTS and HDL. CONCLUSIONS: Urinary Sestrin2 is involved in OSA, and is a paramount marker of OSA severity.
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spelling pubmed-64868962019-05-15 Investigation of Urinary Sestrin2 in Patients with Obstructive Sleep Apnea Bai, Lu Sun, Chunying Zhai, Huifen Chen, Chen Hu, Xiaotian Ye, Xiulin Li, Min Fang, Yan Yang, Weimin Wang, Haoyan Sun, Shibo Lung Sleep Apnea BACKGROUND: Obstructive sleep apnea (OSA) is a disease seriously threatening individual health, which results in serious complications such as hypertension and stroke. These complications are associated with oxidative stress triggered by intermittent hypoxia in OSA. Sestrin2 is a crucial factor involved in oxidative stress. The goal of this study was to investigate if a relationship exists between OSA and Sestrin2. METHODS: We prospectively enrolled 71 subjects, and 16 patients of them with severe OSA completed 4 weeks of nasal continuous positive airway pressure (nCPAP) therapy. We measured and compared the concentration of Sestrin2 in the urine of all subjects, as well as the changes between before and after nCPAP treatment. Additionally, the correlation between Sestrin2 and sleep parameters was analyzed, and the multiple linear regression analysis with stepwise selection was performed to explore the relationship between Sestrin2 and various factors. RESULTS: A total of 71 subjects were enrolled and divided into two groups: OSA group (n = 41), control group (n = 30). The level of urinary Sestrin2 in OSA patients was significantly higher than that of the control group, and increased with the severity of OSA, while it reduced after nCPAP treatment. Additionally, Sestrin2 was positively correlated with apnea/hypopnea index (AHI), oxygen desaturation index, oxygen saturation < 90% percentage of recording time spent (PRTS) and high-density lipoprotein (HDL), while negatively correlated with the lowest oxygen saturation. Importantly, Sestrin2 was independently associated with AHI, oxygen saturation < 90% PRTS and HDL. CONCLUSIONS: Urinary Sestrin2 is involved in OSA, and is a paramount marker of OSA severity. Springer US 2019-02-15 2019 /pmc/articles/PMC6486896/ /pubmed/30770985 http://dx.doi.org/10.1007/s00408-019-00205-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Sleep Apnea
Bai, Lu
Sun, Chunying
Zhai, Huifen
Chen, Chen
Hu, Xiaotian
Ye, Xiulin
Li, Min
Fang, Yan
Yang, Weimin
Wang, Haoyan
Sun, Shibo
Investigation of Urinary Sestrin2 in Patients with Obstructive Sleep Apnea
title Investigation of Urinary Sestrin2 in Patients with Obstructive Sleep Apnea
title_full Investigation of Urinary Sestrin2 in Patients with Obstructive Sleep Apnea
title_fullStr Investigation of Urinary Sestrin2 in Patients with Obstructive Sleep Apnea
title_full_unstemmed Investigation of Urinary Sestrin2 in Patients with Obstructive Sleep Apnea
title_short Investigation of Urinary Sestrin2 in Patients with Obstructive Sleep Apnea
title_sort investigation of urinary sestrin2 in patients with obstructive sleep apnea
topic Sleep Apnea
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486896/
https://www.ncbi.nlm.nih.gov/pubmed/30770985
http://dx.doi.org/10.1007/s00408-019-00205-8
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