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Oxidative Stress-induced Telomere Length Shortening of Circulating Leukocyte in Patients with Obstructive Sleep Apnea

机译:氧化应激诱导的阻塞性睡眠呼吸暂停患者循环白细胞端粒长度缩短

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摘要

The main mechanism of pathogenesis which causes systemic complications in obstructive sleep apnea (OSA) patients is believed to be intermittent hypoxia-induced intermediary effect and it depends on the burden of oxidative stress during sleep. We aimed to search the predictive markers which reflect the burden of systemic oxidative stress in patients with OSA and whether excessive telomere length shortening is a characteristic feature that can assess oxidative stress levels. We used quantitative PCR to measure telomere length using peripheral blood genomic DNA. Telomere lengths were compared in an age- and body mass index (BMI)-dependent manner in 34 healthy volunteers and 43 OSA subjects. We also performed reactive oxygen species assay to measure the concentration of hydrogen peroxide in the peripheral blood of healthy volunteers and OSA subjects. We found that the serum concentration of hydrogen peroxide was considerably higher in OSA patients, and that this was closely related with the severity of OSA. Significantly shortened telomere length was observed in the circulating leukocytes of the peripheral blood of OSA patients, and telomere length shortening was aggravated more acutely in an age- and BMI-dependent manner. An inverse correlation was observed between the concentration of hydrogen peroxide and the telomere length of OSA patients and excessive telomere length shortening was also linked to severity of OSA. The results provided evidence that telomere length shortening or excessive cellular aging might be distinctive in circulating leukocyte of OSA patients and may be an predictive biomarker for reflect the burden of oxidative stress in the peripheral blood of OSA patients.
机译:导致阻塞性睡眠呼吸暂停(OSA)患者系统性并发症的发病机理的主要机制被认为是间歇性缺氧诱导的中间作用,它取决于睡眠中氧化应激的负担。我们旨在搜索预测性标志物,这些标志物可反映OSA患者系统性氧化应激的负担,以及端粒长度过短缩短是否是可评估氧化应激水平的特征。我们使用定量PCR使用外周血基因组DNA测量端粒长度。在34名健康志愿者和43名OSA受试者中,以年龄和体重指数(BMI)依赖性方式比较了端粒长度。我们还进行了活性氧物种分析,以测量健康志愿者和OSA受试者外周血中过氧化氢的浓度。我们发现OSA患者的血清过氧化氢浓度要高得多,这与OSA的严重程度密切相关。在OSA患者外周血循环白细胞中观察到端粒长度显着缩短,并且端粒长度缩短以年龄和BMI依赖性更为严重。观察到过氧化氢的浓度与OSA患者的端粒长度成反比,端粒长度过短也与OSA的严重程度有关。结果提供了证据,端粒长度缩短或过度的细胞衰老在OSA患者的循环白细胞中可能是独特的,并且可能是反映OSA患者外周血氧化应激负担的预测生物标志物。

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