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首页> 外文期刊>Sleep & breathing =: Schlaf & Atmung >Measurement of fractional exhaled nitric oxide and nasal nitric oxide in male patients with obstructive sleep apnea
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Measurement of fractional exhaled nitric oxide and nasal nitric oxide in male patients with obstructive sleep apnea

机译:梗阻性睡眠呼吸暂停患者分数呼出一氧化氮和鼻部一氧化氮的测量

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摘要

Objective Airway inflammation plays an important role in obstructive sleep apnea (OSA); exhaled nitric oxide is regarded as a noninvasive marker of airway inflammation. The aim of this study was to evaluate fractional exhaled nitric oxide (FeNO) and nasal nitric oxide (nNO) in patients with OSA. Methods Seventy-five patients with OSA and 30 health controls were enrolled in this study. FeNO and nNO were measured before and after sleep. Nasal lavage was performed in 31 non-smoking individuals immediately after NO measurement in the morning. The sample of nasal lavage was taken for cell classification and analyzing interleukin 6 (IL-6) and interleukin 8 (IL-8). Results Both FeNO and nNO were significantly higher in OSA (before sleep FeNO 21.08 +/- 8.79 ppb vs.16.90 +/- 6.86 ppb, p = 0.022; after sleep FeNO 25.57 +/- 15.58 ppb vs.18.07 +/- 6.25 ppb, p = 0.003; before sleep nNO 487.03 +/- 115.83 ppb vs. 413.37 +/- 73.10 ppb, p = 0.001; after sleep nNO 550.07 +/- 130.24 ppb vs. 460.43 +/- 109.77 ppb, p < 0.001). Furthermore, in non-smoking OSA, nNO levels were positively correlated with apnea hypopnea index (AHI) and average decrease of pulse arterial oxygen saturation (SpO(2)); after sleep, nNO was also positively associated to recording time with SpO(2) < 90% and negatively associated to minimum SpO(2). Both before and after sleep nNO levels were positively correlated with the percentage of neutrophils in nasal lavage (r = 0.528, p = 0.014; r = 0.702, p < 0.001, respectively). Additionally, before sleep nNO was also positively associated with IL-6 (r = 0.586, p = 0.005) and IL-8 (r = 0.520, p = 0.016) concentration. Conclusion This study sustains the presence of airway inflammation in OSA patients with the increase of FeNO and nNO. The data suggests nNO might have greater value than FeNO since it positively correlated with OSA severity, and nNO is a potential bio-marker of nasal inflammation in non-smoking OSA patients.
机译:客观气道炎症在阻塞性睡眠呼吸暂停(OSA)中起着重要作用;呼出的一氧化氮被认为是气道炎症的非侵入性标记。本研究的目的是在OSA患者中评估分数呼出的一氧化氮(FENO)和鼻部一氧化物(NNO)。方法七十五名患有OSA和30例卫生控制的患者参加了本研究。 FENO和NNO在睡眠前后测量。在早上没有测量后,在31只禁止禁烟个体中患有鼻灌洗。用于细胞分类和分析白细胞介素6(IL-6)和白细胞介素8(IL-8)进行鼻灌洗样品。结果OSA(FENO 21.08 +/- 8.79 PPB,PPB,P = 0.022),FENO和NNO两者(睡眠前21.08 + 8.79 PPB,P = 0.022; 25.57 +/-15.58 PPB vs.18.07 +/- 6.25 PPB ,p = 0.003;睡眠前NNO 487.03 +/- 115.83 PPB与413.37 +/- 73.10 PPB,P = 0.001;睡眠后NNO 550.07 +/- 130.24 PPB与460.43 +/- 109.77 PPB,P <0.001)。此外,在非吸烟的OSA中,NNO水平与呼吸暂停次呼吸症指数(AHI)呈正相关,脉搏动脉氧饱和度的平均降低(SPO(2));在睡眠之后,NNO也与记录时间与SPO(2)<90%的时间呈正相关,且与最小孢子(2)负相关。在睡眠中之前和之后,NNO水平与鼻灌洗中的中性粒细胞的百分比呈正相关(r = 0.528,p = 0.014; r = 0.702,p <0.001分别)。另外,在睡眠中,在睡眠中也与IL-6(r = 0.586,p = 0.005)和IL-8(r = 0.520,p = 0.016)浓度呈正相关。结论本研究维持了OSA患者的气道炎症的存在,增加了FENO和NNO。数据表明,由于与OSA严重程度呈正相关,因此NNO可能具有比FENO更大的值,并且NNO是非吸烟OSA患者中鼻炎的潜在生物标记。

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