Changes of breath volatile organic compounds in healthy volunteers following segmental and inhalation endotoxin challenge

呼出气冷凝液 吸入 四分位间距 呼气 支气管肺泡灌洗 吸入染毒 医学 气体分析呼吸 化学 内科学 哮喘 麻醉 病理 色谱法 肺结核
作者
Olaf Holz,Robert van Vorstenbosch,Frank H. Guenther,Sven Schuchardt,Frederik Trinkmann,Frederik‐Jan van Schooten,Agnieszka Smolinska,Jens M. Hohlfeld
出处
期刊:Journal of Breath Research [IOP Publishing]
卷期号:16 (3): 037102-037102 被引量:8
标识
DOI:10.1088/1752-7163/ac6359
摘要

It is still unclear how airway inflammation affects the breath volatile organic compounds (VOCs) profile in exhaled air. We therefore analyzed breath following well-defined pulmonary endotoxin (lipopolysaccharide, LPS) challenges. Breath was collected from ten healthy non-smoking subjects at eight time points before and after segmental and whole lung LPS inhalation challenge. Four Tenax-TA® adsorption tubes were simultaneously loaded from an aluminum reservoir cylinder and independently analyzed by two research groups using gas chromatography-mass spectrometry. Airway inflammation was assessed in bronchoalveolar lavage (BAL) and in sputum after segmental and inhaled LPS challenge, respectively. Segmental LPS challenge significantly increased the median (interquartile range, IQR) percentage of neutrophils in BAL from 3.0 (4.2) % to 64.0 (7.3) %. The inhalation challenge increased sputum neutrophils from 33.9 (26.8) % to 78.3 (13.5) %. We observed increases in breath aldehydes at both time points after segmental and inhaled LPS challenge. These results were confirmed by an independent laboratory. The longitudinal breath analysis also revealed distinct VOC patterns related to environmental exposures, clinical procedures, and to metabolic changes after food intake. Changes in breath aldehydes suggest a relationship to LPS induced inflammation compatible with lipid peroxidation processes within the lung. Findings from our longitudinal data highlight the need for future studies to better consider the potential impact of the multiple VOCs from detergents, hygiene or lifestyle products a subject is continuously exposed to. We suspect that this very individual 'owncloud' exposure is contributing to an increased variability of breath aldehydes, which might limit a use as inflammatory markers in daily clinical practice.
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