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阻塞性睡眠呼吸暂停中的晚期氧化蛋白产物与缺血修饰白蛋白

Advanced oxidation protein products and ischaemia-modified albumin in obstructive sleep apnea.

作者信息

Ozben Serkan, Huseyinoglu Nergiz, Hanikoglu Ferhat, Guvenc Tolga Sinan, Yildirim Binnaz Zeynep, Cort Aysegul, Ozdem Sebahat, Ozben Tomris

机构信息

Department of Neurology, Bakirkoy Training and Research Hospital for Psychiatry, Neurology and Neurosurgery Diseases, Istanbul, Turkey.

出版信息

Eur J Clin Invest. 2014 Nov;44(11):1045-52. doi: 10.1111/eci.12338. Epub 2014 Oct 4.

Abstract

BACKGROUND

Several studies have shown that obstructive sleep apnea increases incidence of cardiovascular morbidity and mortality. The high systemic oxidative stress in obstructive sleep apnea has been considered as a major pathogenic mechanism leading to cardiovascular disease. Oxidative stress-related lipid and DNA oxidation in obstructive sleep apnea have been reported in the previous studies. In contrast, there is limited and contradictory information regarding protein oxidation in obstructive sleep apnea patients such as ischaemia-modified albumin and advanced oxidation protein products. Therefore, we aimed to investigate plasma ischaemia-modified albumin and advanced oxidation protein products and their correlation with total oxidative status and total antioxidative capacity in the obstructive sleep apnea patients.

METHODS

Plasma ischaemia-modified albumin, advanced oxidation protein products, total oxidative status and total antioxidative capacity were measured in 25 healthy volunteers and 59 obstructive sleep apnea patients diagnosed with polysomnography.

RESULTS

Plasma total antioxidative capacity was significantly lower (P = 0·012) and total oxidative status was significantly higher (P < 0·001) in the patients compared to the controls demonstrating increased oxidative stress in the patients. Plasma advanced oxidation protein products were significantly higher in the patients than the controls (P = 0·024). Plasma ischaemia-modified albumin levels were not statistically different between the obstructive sleep apnea patients and controls (P = 0·74).

CONCLUSIONS

We conclude that high systemic oxidative stress in obstructive sleep apnea is reflected by increased advanced oxidation protein products without causing an increase in ischaemia-modified albumin.

摘要

背景

多项研究表明,阻塞性睡眠呼吸暂停会增加心血管疾病的发病率和死亡率。阻塞性睡眠呼吸暂停中较高的全身氧化应激被认为是导致心血管疾病的主要致病机制。先前的研究报道了阻塞性睡眠呼吸暂停中与氧化应激相关的脂质和DNA氧化。相比之下,关于阻塞性睡眠呼吸暂停患者蛋白质氧化的信息有限且相互矛盾,如缺血修饰白蛋白和晚期氧化蛋白产物。因此,我们旨在研究阻塞性睡眠呼吸暂停患者血浆中的缺血修饰白蛋白和晚期氧化蛋白产物及其与总氧化状态和总抗氧化能力的相关性。

方法

对25名健康志愿者和59名经多导睡眠图诊断为阻塞性睡眠呼吸暂停的患者测量血浆缺血修饰白蛋白、晚期氧化蛋白产物、总氧化状态和总抗氧化能力。

结果

与对照组相比,患者的血浆总抗氧化能力显著降低(P = 0·012),总氧化状态显著升高(P < 0·001),表明患者的氧化应激增加。患者的血浆晚期氧化蛋白产物显著高于对照组(P = 0·024)。阻塞性睡眠呼吸暂停患者与对照组之间的血浆缺血修饰白蛋白水平无统计学差异(P = 0·74)。

结论

我们得出结论,阻塞性睡眠呼吸暂停中较高的全身氧化应激表现为晚期氧化蛋白产物增加,而缺血修饰白蛋白并未增加。

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