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Relationship between HIF-1 and Circadian Clock Proteins in Obstructive Sleep Apnea Patients—Preliminary Study

机译:阻塞性睡眠呼吸暂停患者HIF-1与昼夜节律蛋白的关系-初步研究

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摘要

Obstructive sleep apnea (OSA) is characterized by intermittent hypoxia and associated with the disruption of circadian rhythm. The study aimed to assess the relationship between hypoxia-inducible factor (HIF) subunits, circadian clock proteins, and polysomnography (PSG) variables, in healthy individuals and severe OSA patients. The study included 20 individuals, who underwent PSG and were divided into severe OSA group ( = 10; AHI ≥ 30) and healthy control ( = 10; AHI < 5) based on apnea-hypopnea index (AHI). All participants had their peripheral blood collected in the evening before and the morning after the PSG. HIF-1α, HIF-1β, BMAL1, CLOCK, CRY1, and PER1 protein concertation measurements were performed using ELISA. In a multivariate general linear model with the concentration of all circadian clock proteins as dependent variables, evening HIF-1α protein level was the only significant covariant ( = 0.025). Corrected models were significant for morning and evening PER1 ( = 0.008 and = 0.006, respectively), evening ( = 0.043), and evening BMAL protein level ( = 0.046). In corrected models, evening HIF-1α protein level had an influence only on the evening PER1 protein level. Results suggest that OSA patients are at risk for developing circadian clock disruption. This process might be mediated by subunit α of HIF-1, as its increased protein level is associated with overexpression of circadian clock proteins.
机译:阻塞性睡眠呼吸暂停(OSA)的特点是间歇性缺氧,并与昼夜节律紊乱有关。该研究旨在评估健康个体和严重OSA患者中的缺氧诱导因子(HIF)亚基,昼夜节律蛋白和多导睡眠图(PSG)变量之间的关系。该研究包括20例行PSG的患者,根据呼吸暂停低通气指数(AHI)分为严重OSA组(= 10; AHI≥30)和健康对照组(= 10; AHI <5)。在PSG之前和之后的晚上,所有参与者都采集了外周血。使用ELISA进行HIF-1α,HIF-1β,BMAL1,CLOCK,CRY1和PER1蛋白的一致测定。在所有昼夜节律时钟蛋白的浓度为因变量的多元通用线性模型中,夜间HIF-1α蛋白水平是唯一的显着协变量(= 0.025)。校正后的模型对于PER1早晚(分别为0.008和0.006),傍晚(= 0.043)和傍晚BMAL蛋白水平(= 0.046)很有意义。在校正的模型中,晚上的HIF-1α蛋白水平仅对晚上的PER1蛋白水平有影响。结果表明,OSA患者有发生昼夜节律紊乱的风险。此过程可能由HIF-1的亚基α介导,因为其蛋白水平升高与生物钟蛋白的过表达有关。

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