Brinkman P, van de Pol M A, Gerritsen M G, Bos L D, Dekker T, Smids B S, Sinha A, Majoor C J, Sneeboer M M, Knobel H H, Vink T J, de Jongh F H, Lutter R, Sterk P J, Fens N
Department of Respiratory Medicine, Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Department of Experimental Immunology, Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Clin Exp Allergy. 2017 Sep;47(9):1159-1169. doi: 10.1111/cea.12965. Epub 2017 Jul 10.
Asthma is a chronic inflammatory airway disease, associated with episodes of exacerbations. Therapy with inhaled corticosteroids (ICS) targets airway inflammation, which aims to maintain and restore asthma control. Clinical features are only modestly associated with airways inflammation. Therefore, we hypothesized that exhaled volatile metabolites identify longitudinal changes between clinically stable episodes and loss of asthma control.
To determine whether exhaled volatile organic compounds (VOCs) as measured by gas-chromatography/mass-spectrometry (GC/MS) and electronic nose (eNose) technology discriminate between clinically stable and unstable episodes of asthma.
Twenty-three patients with (partly) controlled mild to moderate persistent asthma using ICS were included in this prospective steroid withdrawal study. Exhaled metabolites were measured at baseline, during loss of control and after recovery. Standardized sampling of exhaled air was performed, after which samples were analysed by GC/MS and eNose. Univariate analysis of covariance (ANCOVA), followed by multivariate principal component analysis (PCA) was used to reduce data dimensionality. Next paired t tests were utilized to analyse within-subject breath profile differences at the different time-points. Finally, associations between exhaled metabolites and sputum inflammation markers were examined.
Breath profiles by eNose showed 95% (21/22) correct classification for baseline vs loss of control and 86% (19/22) for loss of control vs recovery. Breath profiles using GC/MS showed accuracies of 68% (14/22) and 77% (17/22) for baseline vs loss of control and loss of control vs recovery, respectively. Significant associations between exhaled metabolites captured by GC/MS and sputum eosinophils were found (Pearson r≥.46, P<.01).
CONCLUSIONS & CLINICAL RELEVANCE: Loss of asthma control can be discriminated from clinically stable episodes by longitudinal monitoring of exhaled metabolites measured by GC/MS and particularly eNose. Part of the uncovered biomarkers was associated with sputum eosinophils. These findings provide proof of principle for monitoring and identification of loss of asthma control by breathomics.
哮喘是一种慢性气道炎症性疾病,与病情加重发作有关。吸入性糖皮质激素(ICS)治疗针对气道炎症,旨在维持和恢复哮喘控制。临床特征与气道炎症的关联较弱。因此,我们推测呼出的挥发性代谢产物可识别临床稳定期与哮喘控制丧失之间的纵向变化。
确定通过气相色谱/质谱联用仪(GC/MS)和电子鼻(eNose)技术测量的呼出挥发性有机化合物(VOCs)能否区分哮喘临床稳定期和不稳定期。
本前瞻性撤用类固醇研究纳入了23例使用ICS(部分)控制的轻度至中度持续性哮喘患者。在基线、控制丧失期间和恢复后测量呼出代谢产物。进行呼出气体的标准化采样,之后通过GC/MS和eNose对样本进行分析。采用单变量协方差分析(ANCOVA),随后进行多变量主成分分析(PCA)以降低数据维度。接着使用配对t检验分析不同时间点受试者内呼吸图谱差异。最后,检查呼出代谢产物与痰液炎症标志物之间的关联。
eNose的呼吸图谱显示,基线与控制丧失之间的正确分类率为95%(21/22),控制丧失与恢复之间的正确分类率为86%(19/22)。使用GC/MS的呼吸图谱显示,基线与控制丧失之间的准确率分别为68%(14/22),控制丧失与恢复之间的准确率为77%(17/22)。发现GC/MS捕获的呼出代谢产物与痰液嗜酸性粒细胞之间存在显著关联(Pearson r≥.46,P<.01)。
通过对GC/MS尤其是eNose测量的呼出代谢产物进行纵向监测,可将哮喘控制丧失与临床稳定期区分开来。部分发现的生物标志物与痰液嗜酸性粒细胞有关。这些发现为通过呼吸组学监测和识别哮喘控制丧失提供了原理证明。