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P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea
Objective: Obstructive sleep apnea (OSA) is characterized by nocturnal intermittent hypoxemia and linked to oxidative stress. Evidence demonstrated that p66Shc plays a key role in regulating oxidative stress. This study aimed to investigate the expression of p66Shc in peripheral blood mononuclear ce...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087631/ https://www.ncbi.nlm.nih.gov/pubmed/37057208 http://dx.doi.org/10.7150/ijms.80343 |
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author | Lyu, Xing Cai, Jingyao Yan, Rongxuan Huang, Peiying Gong, Hui Peng, Jieting Liu, Yang Li, Shizhen Tan, Shengyu Hu, Min Zhang, Xiangyu |
author_facet | Lyu, Xing Cai, Jingyao Yan, Rongxuan Huang, Peiying Gong, Hui Peng, Jieting Liu, Yang Li, Shizhen Tan, Shengyu Hu, Min Zhang, Xiangyu |
author_sort | Lyu, Xing |
collection | PubMed |
description | Objective: Obstructive sleep apnea (OSA) is characterized by nocturnal intermittent hypoxemia and linked to oxidative stress. Evidence demonstrated that p66Shc plays a key role in regulating oxidative stress. This study aimed to investigate the expression of p66Shc in peripheral blood mononuclear cells (PBMCs) of patients with OSA and the association with polysomnographic parameters. Methods: Fifty-four OSA subjects and 19 no OSA controls were enrolled in this study. All the subjects underwent standard polysomnography. P66Shc mRNA and protein levels in the PBMCs were detected by quantitative real-time polymerase chain reaction and western blotting. Plasma 3-nitrotyrosine (3-NT), oxidized low density lipoprotein (oxLDL), and advanced oxidation protein products (AOPP) were measured by ELISA method. Results: P66Shc mRNA and protein levels in PBMCs were significantly higher in OSA patients than in controls. P66Shc mRNA was positively correlated with plasma 3-NT, oxLDL, AOPP, hypopnea index (AHI), oxygen desaturation index (ODI), percentage of total sleep time with oxygen saturation (SaO(2)) below 90% (CT90), epworth sleepiness scale (ESS) and lymphocytes; negatively correlated with lowest SaO(2) (LSaO(2)) and mean SaO(2) (MSaO(2)). Further multivariate linear regression analysis showed that p66Shc mRNA levels were independently associated with AHI, MSaO(2) and CT90. Conclusions: Oxidative stress regulator p66Shc may play a role in the pathophysiology of OSA and might serve as a potential biomarker for this disease. |
format | Online Article Text |
id | pubmed-10087631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-100876312023-04-12 P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea Lyu, Xing Cai, Jingyao Yan, Rongxuan Huang, Peiying Gong, Hui Peng, Jieting Liu, Yang Li, Shizhen Tan, Shengyu Hu, Min Zhang, Xiangyu Int J Med Sci Research Paper Objective: Obstructive sleep apnea (OSA) is characterized by nocturnal intermittent hypoxemia and linked to oxidative stress. Evidence demonstrated that p66Shc plays a key role in regulating oxidative stress. This study aimed to investigate the expression of p66Shc in peripheral blood mononuclear cells (PBMCs) of patients with OSA and the association with polysomnographic parameters. Methods: Fifty-four OSA subjects and 19 no OSA controls were enrolled in this study. All the subjects underwent standard polysomnography. P66Shc mRNA and protein levels in the PBMCs were detected by quantitative real-time polymerase chain reaction and western blotting. Plasma 3-nitrotyrosine (3-NT), oxidized low density lipoprotein (oxLDL), and advanced oxidation protein products (AOPP) were measured by ELISA method. Results: P66Shc mRNA and protein levels in PBMCs were significantly higher in OSA patients than in controls. P66Shc mRNA was positively correlated with plasma 3-NT, oxLDL, AOPP, hypopnea index (AHI), oxygen desaturation index (ODI), percentage of total sleep time with oxygen saturation (SaO(2)) below 90% (CT90), epworth sleepiness scale (ESS) and lymphocytes; negatively correlated with lowest SaO(2) (LSaO(2)) and mean SaO(2) (MSaO(2)). Further multivariate linear regression analysis showed that p66Shc mRNA levels were independently associated with AHI, MSaO(2) and CT90. Conclusions: Oxidative stress regulator p66Shc may play a role in the pathophysiology of OSA and might serve as a potential biomarker for this disease. Ivyspring International Publisher 2023-02-13 /pmc/articles/PMC10087631/ /pubmed/37057208 http://dx.doi.org/10.7150/ijms.80343 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Lyu, Xing Cai, Jingyao Yan, Rongxuan Huang, Peiying Gong, Hui Peng, Jieting Liu, Yang Li, Shizhen Tan, Shengyu Hu, Min Zhang, Xiangyu P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea |
title | P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea |
title_full | P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea |
title_fullStr | P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea |
title_full_unstemmed | P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea |
title_short | P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea |
title_sort | p66shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087631/ https://www.ncbi.nlm.nih.gov/pubmed/37057208 http://dx.doi.org/10.7150/ijms.80343 |
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