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8-isorpostanes – markers for oxidative stress in obstructive sleep apnea patients with systolic dysfunction

机译:8-isorpostanes –收缩功能障碍的阻塞性睡眠呼吸暂停患者氧化应激的标志物

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Objective: Increased oxidative stress is considered to be an independent risk factor for cardiovascular diseases, but remains disputed in obstructive sleep apnea (OSA). Among oxidative stress markers, isorpostanes are considered to be the most sensitive and specific. Aims: The aim of the study was to compare urinary isorpostanes in patients with OSA and systolic dysfunction to patients with OSA and preserved ejection fraction (EF) and determine their role as markers for increased oxidative stress and early cardiac damage. Materials and methods: Urinary 8F2-isorpostanes were measured in 30 patients with OSA and mild systolic dysfunction (EF = 45.7% ± 6.17%) and compared to 15 patients with OSA and normal EF (EF = 60.3% ± 6.3%). Univariate regression analysis was performed to find predictors of left systolic dysfunction. Correlations between 8-isorpostanes, anthropometric, metabolic, and sleep study characteristics were explored. In addition, in 19 patients the effect of bilevel positive airway pressure (BiPAP) therapy was evaluated during a 3 month follow-up. Markers of hemodynamic stress, N-terminal prohormone of brain natriuretic peptide and oxidative stress, measured by 8-isorpostanes were compared before and after the follow-up. Results: Urinary levels of 8-isorpostanes were significantly higher in the group with mild systolic dysfunction in comparison to the controls with preserved EF (0.149 versus 0.049 pg/μL, P = 0.023). The regression analysis did not define them as predictors for left systolic dysfunction. Their urinary concentration correlated best to the average desaturation index (P = 0.043). Urinary 8-isorpostanes decreased as a result of BiPAP therapy after three months of follow-up (0.164 versus 0.098 pg/μL, P = 0.011). Conclusion: Urinary isorpostanes are reliable markers for chronic intermittent hypoxia and oxidative stress in OSA patients. They may be of clinical application for the early detection of patients at risk for cardiovascular damage and could help in the monitoring of the restoration of oxidative balance.
机译:目的:氧化应激的增加被认为是心血管疾病的独立危险因素,但在阻塞性睡眠呼吸暂停(OSA)中仍然存在争议。在氧化应激标记中,异二十烷被认为是最敏感和最特异的。目的:本研究的目的是比较OSA和收缩功能障碍的OSA患者和保留射血分数(EF)的尿异二十烷,并确定其作为增加氧化应激和早期心脏损害的标志物的作用。材料和方法:对30例OSA轻度收缩功能不全(EF = 45.7%±6.17%)的患者进行尿液8F2-异二十烷烷的测定,并与15例OSA EF正常的患者(EF = 60.3%±6.3%)进行了比较。进行单因素回归分析以发现左收缩功能障碍的预测因子。探索了8-异戊烷,人体测量,代谢和睡眠研究特征之间的相关性。此外,在3个月的随访中评估了19例患者的双水平气道正压通气(BiPAP)治疗的效果。在随访前后比较了通过8-异雌烷测量的血流动力学应激,脑钠肽前体N端激素和氧化应激的指标。结果:与保留EF的对照组相比,轻度收缩功能不全组的尿中8-异雌烷含量显着更高(0.149对0.049 pg /μL,P = 0.023)。回归分析未将其定义为左收缩功能障碍的预测指标。他们的尿液浓度与平均去饱和指数相关性最好(P = 0.043)。随访三个月后,由于BiPAP治疗,尿中的8-异二十烷减少(0.164对0.098 pg /μL,P = 0.011)。结论:尿异二十烷是OSA患者慢性间歇性缺氧和氧化应激的可靠指标。它们可能在临床上用于早期发现有心血管损害风险的患者,并可能有助于监测氧化平衡的恢复。

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