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P66Shc is increased in peripheral blood mononuclear cells of the patients with obstructive sleep apnea. | LitMetric

AI Article Synopsis

  • Obstructive sleep apnea (OSA) causes intermittent low oxygen levels during sleep, which leads to oxidative stress, and the study focuses on the role of p66Shc in this process.
  • The research involved 54 OSA patients and 19 control subjects, measuring p66Shc levels in blood cells and various oxidative stress indicators through standard lab methods.
  • Results showed that p66Shc levels were significantly increased in OSA patients and were linked to key sleep-related factors, suggesting its potential as a biomarker for OSA.

Article Abstract

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. 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. 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) below 90% (CT90), epworth sleepiness scale (ESS) and lymphocytes; negatively correlated with lowest SaO (LSaO) and mean SaO (MSaO). Further multivariate linear regression analysis showed that p66Shc mRNA levels were independently associated with AHI, MSaO and CT90. Oxidative stress regulator p66Shc may play a role in the pathophysiology of OSA and might serve as a potential biomarker for this disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087631PMC
http://dx.doi.org/10.7150/ijms.80343DOI Listing

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