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Obstructive Sleep Apnea, oxidative stress, inflammation and endothelial dysfunction-An overview of predictive laboratory biomarkers

机译:阻塞性睡眠呼吸暂停,氧化应激,炎症和内皮功能障碍 - 预测实验室生物标志物的概述

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OBJECTIVE: Obstructive Sleep Apnea (OSA) represents an emerging public health concern with great impact on cardiovascular state. Oxidative stress (OS), inflammation and altered Nitric Oxide (NO) production are recognized as prominent mechanisms of many acute and chronic diseases and even of the normal aging process. They are investigated as major pathophysiological processes in OSA through the analysis and comparison of significative and validated biomarkers. MATERIALS AND METHODS: The review is developed using as key terms “sleep apnea”, “oxidative stress”, “inflammation”, and “endothelial dysfunction”. Included studies must have followed the American Academy of Sleep Medicine guidelines according to the diagnosis and classification of OSA. Lipid, protein and DNA oxidation products, PCR, IL-6, IL-8, TNF-α, NO and nitrosative stress compounds, and endothelial functioning tests have been detected for their contribution in OSA along the last 3 decades. RESULTS: Nocturnal intermittent hypoxia has emerged to be significantly associated to oxidative/nitrosative stress, increase in pro-inflammatory markers, imbalance in NO production, and endothelium impairment. Body Mass Index (BMI) contribution needs further clarifications. Continuous Positive Airway Pressure (CPAP) therapy has demonstrated beneficial effects on vascular function and pro-inflammatory milieu in OSA. CONCLUSIONS: Oxidative stress and Inflammation significantly correlate with OSA; similarly, vascular functioning is impaired in accordance to unregulated levels of NO and derived compounds. Continuous Positive Airway Pressure markedly improves oxidative stress, inflammation and endothelial dysfunction in OSA.
机译:目的:阻塞性睡眠呼吸暂停(OSA)代表了对心血管状态产生巨大影响的新兴公共卫生问题。氧化应激(OS),炎症和改变的一氧化氮(NO)产生被认为是许多急性和慢性疾病的突出机制,甚至是正常的老化过程。通过分析和比较,在OSA中被调查为主要病理生理过程,并进行了意义和验证的生物标志物。材料和方法:审查是使用关键术语“睡眠呼吸暂停”,“氧化应激”,“炎症”和“内皮功能障碍”开发的。包括的研究必须遵循美国睡眠学科指南,根据OSA的诊断和分类。脂质,蛋白质和DNA氧化产物,PCR,IL-6,IL-8,TNF-α,NO和亚硝酸盐胁迫化合物,并在过去3个十年中检测到它们在OSA的贡献中被检测到内皮功能测试。结果:夜间间歇性缺氧已出现明显与氧化/亚硝化应激,促炎症标志物增加,无产量不平衡,内皮损伤。体重指数(BMI)贡献需要进一步澄清。连续正气道压力(CPAP)治疗对OSA的血管功能和促炎环境有益。结论:氧化应激和炎症与OSA显着相关;类似地,根据不受管和衍生的化合物的未调节水平损害血管功能。连续正气道压力显着提高了OSA的氧化应激,炎症和内皮功能障碍。

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