Identification of a characteristic VOCs pattern in the exhaled breath of post-COVID subjects: are metabolic alterations induced by the infection still detectable?

IF 3.7 4区 医学 Q1 BIOCHEMICAL RESEARCH METHODS
Alessia DI Gilio, Jolanda Palmisani, Arcangelo Picciariello, Carlo Zambonin, Antonella Aresta, Nicoletta De Vietro, Silvana Angela Franchini, Gianrocco Ventrella, Marirosa Nisi, Sabina Licen, Pierluigi Barbieri, Donato Altomare, Gianluigi de Gennaro
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引用次数: 0

Abstract

SARS-CoV-2 is expected to cause metabolic alterations due to viral replication and the host immune response resulting in increase of cytokine secretion and cytolytic activity. The present prospective observational study is addressed at exploring the potentialities of breath analysis in discrimination between patients with a documented previous history of symptomatic SARS-CoV-2 infection and, at the moment of the enrollment, exhibiting a negative nasopharyngeal swab and acquired immunity (post-COVID) and healthy subjects with no evidence of previous SARS-CoV-2 infection (no-COVID). The main purpose is to understand if traces of metabolic alterations induced during the acute phase of the infection are still detectable after negativization, in the form of a characteristic volatile organic compound (VOC) pattern. An overall number of 60 volunteers aged between 25 and 70 years were enrolled in the study (post-COVID: n.30; no-COVID: n. 30), according to well-determined criteria. Breath and ambient air samples were collected by means of an automated sampling system (Mistral) and analyzed by thermal desorption-gas chromatography-mass spectrometry (TD-GC/MS). Statistical tests (Wilcoxon/Kruskal-Wallis test) and multivariate data analysis (principal component analysis (PCA), linear discriminant analysis) were performed on data sets. Among all compounds detected (76 VOCs in 90% of breath samples), 5 VOCs (1-propanol, isopropanol, 2-(2-butoxyethoxy)ethanol, propanal and 4-(1,1-dimethylpropyl)phenol) showed abundances in breath samples collected from post-COVID subjects significantly different with respect to those collected from no-COVID group (Wilcoxon/Kruskal-Wallis test,p-values <0.05). Although not completely satisfactory separation between the groups was obtained, variables showing significant differences between the two groups and higher loadings for PCA are recognized biomarkers of COVID-19, according to previous studies in literature. Therefore, based on the outcomes obtained, traces of metabolic alterations induced by SARS-CoV-2 infection are still detectable after negativization. This evidence raises questions about the eligibility of post-COVID subjects in observational studies addressed at the detection of COVID-19. (Ethical Committee Registration number: 120/AG/11).

covid后受试者呼出气体中挥发性有机化合物特征模式的识别:感染引起的代谢改变是否仍可检测到?
SARS-CoV-2预计会由于病毒复制和宿主免疫反应而引起代谢改变,从而导致细胞因子分泌和细胞溶解活性增加。本前瞻性观察性研究旨在探索呼吸分析在区分有记录的既往有症状的SARS-CoV-2感染史的患者和在入组时表现为鼻咽拭子阴性并获得免疫的患者(covid后)与没有既往SARS-CoV-2感染证据的健康受试者(无covid)之间的潜力。主要目的是了解在感染急性期诱导的代谢改变的痕迹是否在阴性后仍可检测到,以特征挥发性有机化合物(VOC)模式的形式。总共有60名年龄在25至70岁之间的志愿者参加了这项研究(covid后:n.30;无covid: n. 30),根据明确的标准。呼吸和周围空气样本通过自动采样系统(Mistral)收集,并通过热解吸-气相色谱-质谱(TD-GC/MS)分析。对数据集进行统计检验(Wilcoxon/Kruskal-Wallis检验)和多变量数据分析(主成分分析(PCA)、线性判别分析)。在所有检测到的化合物中(90%的呼气样本中有76种VOCs), 5种VOCs(1-丙醇、异丙醇、2-(2-丁氧乙氧基)乙醇、丙醛和4-(1,1-二甲基丙基)苯酚)在新冠肺炎后受试者的呼气样本中的丰度与未感染新冠肺炎的受试者有显著差异(Wilcoxon/Kruskal-Wallis检验,p值)
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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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