Xylometazoline-induced change in aspirated nasal nitric oxide detects obstructed paranasal ostia.

IF 3.7 4区 医学 Q1 BIOCHEMICAL RESEARCH METHODS Journal of breath research Pub Date : 2025-01-28 DOI:10.1088/1752-7163/ada8cf
Pekka Tamminen, Ilkka Kivekäs, Jura Numminen, Jorma Järnstedt, Markus Rautiainen, Lauri Lehtimäki
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Abstract

The concentrations of nasal nitric oxide (nNO) vary in patients with chronic rhinosinusitis (CRS) supposedly depending upon whether the paranasal ostia are open or obstructed. Our aim was to assess whether nNO levels and their response to topical xylometazoline (a local vasoconstrictor used to alleviate nasal congestion) in patients with CRS differ between those with open or obstructed ostia and if the results were altered by the use of nasal corticosteroids. Sixty-six patients with CRS (43% with nasal polyps) or recurrent acute rhinosinusitis and 23 healthy controls were included. Nasal NO was measured (EcoMedics CLD 88p analyser) before and after two xylometazoline sprays during three consecutive visits: with the medication they were using when they were referred, after 4 weeks of medication pause, and after 4 weeks of using intranasal fluticasone propionate. The relative difference between the nNO before and after dosing of xylometazoline was calculated, and ostial obstruction was evaluated with cone-beam computed tomography at every visit. The nNO measurements were lowest in the patients with CRS and obstructed paranasal ostia. The presence or absence of nasal polyps did not affect the results. Xylometazoline did not significantly affect nNO in the subjects with obstructed ostia, but there was a significant reduction of nNO in those with open ostia. The Xylometazoline-induced change in nNO between the groups with open or obstructed ostia was significantly different at each visit: 'on previous medication' 10% (-5-25) versus -14% (-19 to -9),p= 0.004, 'after medication pause' 6% (-5-17) versus -16% (-23 to -9),p= 0.001 and 'after regular fluticasone spray' 6% (-3-15) versus -9% (-16 to -3),p= 0.04. The native nNO and xylometazoline-induced change in nNO can be used to detect the status of ostial obstruction in patients with CRS irrespective of their topical corticosteroid usage.

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木甲咪唑啉诱导的吸入性鼻一氧化氮变化检测鼻副口梗阻。
背景:慢性鼻窦炎(CRS)患者鼻腔一氧化氮(nNO)浓度的变化可能取决于鼻副口是否开放或阻塞。我们的目的是评估nNO水平及其对外用xyylometazoline(一种用于缓解鼻塞的局部血管收缩剂)的反应是否与开放或阻塞的CRS患者不同,以及使用鼻皮质类固醇是否会改变结果。方法:66名CRS患者(43%患有鼻息肉)或复发性急性鼻窦炎患者和23名健康对照者。在连续三次就诊期间,在两次木美唑啉喷雾前后测量鼻腔NO (EcoMedics CLD 88p分析仪):使用他们转诊时使用的药物,停药四周后,鼻内使用丙酸氟替卡松四周后。计算木美唑啉给药前后nNO的相对差异,并在每次就诊时用锥形束计算机断层扫描评估口梗阻。结果:CRS合并鼻窦口梗阻患者的nNO水平最低。有无鼻息肉不影响结果。木美唑啉对闭口组的nNO无显著影响,但对开放组的nNO有显著降低。每次就诊时,木美唑啉引起的nNO变化在开放或阻塞的两组之间有显著差异:“先前用药”组为10%(-5 - 25)对-14% (-19 -9),p=0.004,“暂停用药”组为6%(-5 - 17)对-16% (-23 -9),p=0.001,“常规氟替卡松喷施后”组为6%(-3 - 15)对-9% (-16 -3),p=0.04。结论:无论是否使用外用皮质类固醇,天然一氧化氮和木美唑啉诱导的一氧化氮变化均可用于检测CRS患者的口梗阻状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of breath research
Journal of breath research BIOCHEMICAL RESEARCH METHODS-RESPIRATORY SYSTEM
CiteScore
7.60
自引率
21.10%
发文量
49
审稿时长
>12 weeks
期刊介绍: Journal of Breath Research is dedicated to all aspects of scientific breath research. The traditional focus is on analysis of volatile compounds and aerosols in exhaled breath for the investigation of exogenous exposures, metabolism, toxicology, health status and the diagnosis of disease and breath odours. The journal also welcomes other breath-related topics. Typical areas of interest include: Big laboratory instrumentation: describing new state-of-the-art analytical instrumentation capable of performing high-resolution discovery and targeted breath research; exploiting complex technologies drawn from other areas of biochemistry and genetics for breath research. Engineering solutions: developing new breath sampling technologies for condensate and aerosols, for chemical and optical sensors, for extraction and sample preparation methods, for automation and standardization, and for multiplex analyses to preserve the breath matrix and facilitating analytical throughput. Measure exhaled constituents (e.g. CO2, acetone, isoprene) as markers of human presence or mitigate such contaminants in enclosed environments. Human and animal in vivo studies: decoding the ''breath exposome'', implementing exposure and intervention studies, performing cross-sectional and case-control research, assaying immune and inflammatory response, and testing mammalian host response to infections and exogenous exposures to develop information directly applicable to systems biology. Studying inhalation toxicology; inhaled breath as a source of internal dose; resultant blood, breath and urinary biomarkers linked to inhalation pathway. Cellular and molecular level in vitro studies. Clinical, pharmacological and forensic applications. Mathematical, statistical and graphical data interpretation.
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