Tang Zhifeng, Yang Jianming, Xu Xin, Zhang Keda, Wang Huiling, Luo Xin, Fang Mingliang, Huan Tao, Li Xue
College of Environment and Climate, Institute of Mass Spectrometry and Atmospheric Environment, Guangdong Provincial Key Laboratory of Speed Capability Research, Jinan University, Guangzhou 510632, China.
Guangdong A-HealthX Technologies Co., Ltd., Dongguan 523830, China.
Environ Health (Wash). 2025 Mar 5;3(6):596-604. doi: 10.1021/envhealth.4c00248. eCollection 2025 Jun 20.
Breath metabolomics enables noninvasive and rapid acquisition of metabolic information by detecting volatile organic compounds (VOCs) in exhaled breath. Secondary electrospray ionization high-resolution tandem mass spectrometry (SESI-HRMS/MS) offers the highest coverage for detecting breath metabolites among current real-time breath analysis techniques. Although it has been generally recognized that metabolites in breath originate from the blood, a molecular-level understanding of the characteristics of metabolites in both breath and blood remains insufficient. In this study, nontargeted analyses of breath and blood samples from 11 healthy volunteers were performed using SESI-HRMS/MS and ultrahigh performance liquid chromatography electrospray ionization high-resolution tandem mass spectrometry (UHPLC-ESI-HRMS/MS), respectively. Tandem mass spectrometry was employed for metabolite annotation. Twenty-six breath-unique metabolites and 73 blood-unique metabolites were identified. Besides, seven metabolites were found in both breath and blood, including 7-oxabicyclo [2.2.1] heptane, levulinic acid, indole, pyroglutamic acid, malic acid, glutamic acid, and histidine. Intriguingly, the correlation of these metabolites between breath and blood was low ( < 0.4 or > 0.05). Among all the confirmed metabolites, breath metabolites exhibit higher volatility according to their water-gas partition coefficient (log ) compared to blood metabolites. In addition, gender-derived differences in breath were significantly smaller than blood. In summary, this study indicates that breath metabolites are likely to offer complementary information on blood metabolites. When combined with blood metabolomics, this would be advantageous for the appropriate application of breath metabolomics in life sciences, such as in biomarker discovery.
呼气代谢组学通过检测呼出气体中的挥发性有机化合物(VOCs),能够实现代谢信息的无创快速获取。二次电喷雾电离高分辨率串联质谱(SESI-HRMS/MS)在当前实时呼气分析技术中,对呼气代谢物的检测覆盖范围最广。尽管人们普遍认为呼出气体中的代谢物源自血液,但在分子水平上,对呼出气体和血液中代谢物特征的了解仍不充分。在本研究中,分别使用SESI-HRMS/MS和超高效液相色谱电喷雾电离高分辨率串联质谱(UHPLC-ESI-HRMS/MS),对11名健康志愿者的呼出气体和血液样本进行了非靶向分析。采用串联质谱进行代谢物注释。鉴定出26种呼出气体特有的代谢物和73种血液特有的代谢物。此外,在呼出气体和血液中均发现了7种代谢物,包括7-氧杂双环[2.2.1]庚烷、乙酰丙酸、吲哚、焦谷氨酸、苹果酸、谷氨酸和组氨酸。有趣的是,这些代谢物在呼出气体和血液之间的相关性较低(<0.4或>0.05)。在所有已确认的代谢物中,根据其水-气分配系数(log ),呼出气体代谢物的挥发性高于血液代谢物。此外,呼出气体中因性别产生的差异明显小于血液。总之,本研究表明呼出气体代谢物可能为血液代谢物提供补充信息。与血液代谢组学相结合,这将有利于呼气代谢组学在生命科学中的适当应用,如生物标志物发现。