University Children's Hospital Basel, University of Basel, Spitalstr. 33, 4056, Basel, Switzerland.
Department of Biomedical Engineering, University of Basel, Gewerbestr. 14, 4123, Allschwil, Switzerland.
Anal Bioanal Chem. 2019 Jul;411(19):4883-4898. doi: 10.1007/s00216-019-01764-8. Epub 2019 Apr 15.
Despite the attractiveness of breath analysis as a non-invasive means to retrieve relevant metabolic information, its introduction into routine clinical practice remains a challenge. Among all the different analytical techniques available to interrogate exhaled breath, secondary electrospray ionization high-resolution mass spectrometry (SESI-HRMS) offers a number of advantages (e.g., real-time, yet wide, metabolome coverage) that makes it ideal for untargeted and targeted studies. However, so far, SESI-HRMS has relied mostly on lab-built prototypes, making it difficult to standardize breath sampling and subsequent analysis, hence preventing further developments such as multi-center clinical studies. To address this issue, we present here a number of new developments. In particular, we have characterized a new SESI interface featuring real-time readout of critical exhalation parameters such as CO, exhalation flow rate, and exhaled volume. Four healthy subjects provided breath specimens over a period of 1 month to characterize the stability of the SESI-HRMS system. A first assessment of the repeatability of the system using a gas standard revealed a coefficient of variation (CV) of 2.9%. Three classes of aldehydes, namely 4-hydroxy-2-alkenals, 2-alkenals and 4-hydroxy-2,6-alkedienals-hypothesized to be markers of oxidative stress-were chosen as representative metabolites of interest to evaluate the repeatability and reproducibility of this breath analysis analytical platform. Median and interquartile ranges (IQRs) of CVs for CO, exhalation flow rate, and exhaled volume were 3.2% (1.5%), 3.1% (1.9%), and 5.0% (4.6%), respectively. Despite the high repeatability observed for these parameters, we observed a systematic decay in the signal during repeated measurements for the shorter fatty aldehydes, which eventually reached a steady state after three/four repeated exhalations. In contrast, longer fatty aldehydes showed a steady behavior, independent of the number of repeated exhalation maneuvers. We hypothesize that this highly molecule-specific and individual-independent behavior may be explained by the fact that shorter aldehydes (with higher estimated blood-to-air partition coefficients; approaching 100) mainly get exchanged in the airways of the respiratory system, whereas the longer aldehydes (with smaller estimated blood-to-air partition coefficients; approaching 10) are thought to exchange mostly in the alveoli. Exclusion of the first three exhalations from the analysis led to a median CV (IQR) of 6.7 % (5.5 %) for the said classes of aldehydes. We found that such intra-subject variability is in general much lower than inter-subject variability (median relative differences between subjects 48.2%), suggesting that the system is suitable to capture such differences. No batch effect due to sampling date was observed, overall suggesting that the intra-subject variability measured for these series of aldehydes was biological rather than technical. High correlations found among the series of aldehydes support this notion. Finally, recommendations for breath sampling and analysis for SESI-HRMS users are provided with the aim of harmonizing procedures and improving future inter-laboratory comparisons. Graphical abstract.
尽管呼吸分析作为一种非侵入性手段来获取相关代谢信息具有吸引力,但将其引入常规临床实践仍然是一个挑战。在可用于检测呼气的所有不同分析技术中,二级电喷雾电离高分辨率质谱(SESI-HRMS)具有许多优势(例如实时但广泛的代谢组覆盖范围),使其非常适合于非靶向和靶向研究。然而,到目前为止,SESI-HRMS 主要依赖于实验室构建的原型,这使得呼吸采样和后续分析难以标准化,从而阻止了进一步的发展,例如多中心临床研究。为了解决这个问题,我们在这里提出了一些新的发展。特别是,我们已经对一种新的 SESI 接口进行了表征,该接口具有实时读取 CO、呼气流量和呼气量等关键呼气参数的功能。四名健康受试者在一个月的时间内提供了呼吸样本,以表征 SESI-HRMS 系统的稳定性。使用气体标准对系统的重复性进行了首次评估,结果显示变异系数(CV)为 2.9%。选择了三种类别的醛,即 4-羟基-2-烯醛、2-烯醛和 4-羟基-2,6-二烯醛,它们被认为是氧化应激的标志物,作为感兴趣的代表性代谢物来评估这种呼吸分析分析平台的重复性和重现性。CO、呼气流量和呼气量的中位数和四分位距(IQR)分别为 3.2%(1.5%)、3.1%(1.9%)和 5.0%(4.6%)。尽管这些参数的重复性很高,但我们观察到在重复测量过程中较短的脂肪酸醛的信号会出现系统衰减,最终在重复呼气 3/4 次后达到稳定状态。相比之下,较长的脂肪酸醛表现出稳定的行为,与重复呼气的次数无关。我们假设这种高度分子特异性和个体独立性的行为可能是由于较短的醛(估计的血/气分配系数较高;接近 100)主要在呼吸系统的气道中交换,而较长的醛(估计的血/气分配系数较小;接近 10)则主要在肺泡中交换。从分析中排除前三次呼气会导致所述醛类的中位数 CV(IQR)为 6.7%(5.5%)。我们发现,这种个体内变异性通常比个体间变异性低得多(个体间中位数相对差异为 48.2%),这表明该系统适合捕捉这种差异。总体而言,未观察到由于采样日期引起的批次效应,这表明为这些醛系列测量的个体内变异性是生物学的而不是技术的。醛系列之间发现的高相关性支持了这一观点。最后,为 SESI-HRMS 用户提供了呼吸采样和分析建议,旨在协调程序并提高未来的实验室间比较。