Exhaled breath condensate profiles of U.S. Navy divers following prolonged hyperbaric oxygen (HBO) and nitrogen-oxygen (Nitrox) chamber exposures.

IF 3.7 4区 医学 Q1 BIOCHEMICAL RESEARCH METHODS Journal of breath research Pub Date : 2023-06-12 DOI:10.1088/1752-7163/acd715
David M Fothergill, Eva Borras, Mitchell M McCartney, Edward S Schelegle, Cristina E Davis
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Abstract

Prolonged exposure to hyperbaric hyperoxia can lead to pulmonary oxygen toxicity (PO2tox). PO2tox is a mission limiting factor for special operations forces divers using closed-circuit rebreathing apparatus and a potential side effect for patients undergoing hyperbaric oxygen (HBO) treatment. In this study, we aim to determine if there is a specific breath profile of compounds in exhaled breath condensate (EBC) that is indicative of the early stages of pulmonary hyperoxic stress/PO2tox. Using a double-blind, randomized 'sham' controlled, cross-over design 14 U.S. Navy trained diver volunteers breathed two different gas mixtures at an ambient pressure of 2 ATA (33 fsw, 10 msw) for 6.5 h. One test gas consisted of 100% O2(HBO) and the other was a gas mixture containing 30.6% O2with the balance N2(Nitrox). The high O2stress dive (HBO) and low O2stress dive (Nitrox) were separated by at least seven days and were conducted dry and at rest inside a hyperbaric chamber. EBC samples were taken immediately before and after each dive and subsequently underwent a targeted and untargeted metabolomics analysis using liquid chromatography coupled to mass spectrometry (LC-MS). Following the HBO dive, 10 out of 14 subjects reported symptoms of the early stages of PO2tox and one subject terminated the dive early due to severe symptoms of PO2tox. No symptoms of PO2tox were reported following the nitrox dive. A partial least-squares discriminant analysis of the normalized (relative to pre-dive) untargeted data gave good classification abilities between the HBO and nitrox EBC with an AUC of 0.99 (±2%) and sensitivity and specificity of 0.93 (±10%) and 0.94 (±10%), respectively. The resulting classifications identified specific biomarkers that included human metabolites and lipids and their derivatives from different metabolic pathways that may explain metabolomic changes resulting from prolonged HBO exposure.

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美国海军潜水员在长期暴露于高压氧(HBO)和氮氧(Nitrox)舱之后的呼出气体冷凝物概况。
长期暴露于高压氧环境中会导致肺氧中毒(PO2tox)。PO2tox是特种作战部队潜水员使用闭路再呼吸设备执行任务时的一个限制因素,也是接受高压氧(HBO)治疗的患者的一个潜在副作用。在这项研究中,我们旨在确定呼出气体冷凝物(EBC)中的化合物是否存在特定的呼吸曲线,以指示肺高氧应激/PO2tox 的早期阶段。通过双盲、随机 "假 "对照、交叉设计,14 名受过训练的美国海军潜水员志愿者在 2 ATA(33 fsw,10 msw)的环境压力下呼吸了 6.5 小时两种不同的混合气体。一种测试气体是 100% 的氧气(HBO),另一种是含 30.6% 氧气的混合气体,其余为 N2(Nitrox)。高氧气压力潜水(HBO)和低氧气压力潜水(Nitrox)至少间隔七天,并在高压氧舱内干燥和静止状态下进行。每次潜水前后立即采集 EBC 样本,随后使用液相色谱耦合质谱法(LC-MS)进行有针对性和无针对性的代谢组学分析。在 HBO 潜水之后,14 名受试者中有 10 人报告出现了 PO2tox 早期症状,一名受试者因出现严重的 PO2tox 症状而提前结束了潜水。硝氧潜水后没有出现 PO2tox 症状。对归一化(相对于潜水前)非目标数据进行偏最小二乘法判别分析后,HBO 和氮氧 EBC 的分类能力良好,AUC 为 0.99(±2%),灵敏度和特异度分别为 0.93(±10%)和 0.94(±10%)。分类结果确定了特定的生物标志物,其中包括来自不同代谢途径的人体代谢物和脂质及其衍生物,这些生物标志物可以解释长期暴露于 HBO 导致的代谢组学变化。
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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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