Study on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumonia

Abstract Background Aspiration pneumonia (AP) is a type of lung inflammation caused by the aspiration of food, oropharyngeal secretions, or gastric contents. This condition is particularly common in older adults and individuals with impaired swallowing or consciousness. While the diagnosis of AP rel...

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Main Authors: Lianghui Chen, Yazhen Chen, Fansen Lin, Jianbao Wang, Hongzhi Gao, Yuqi Liu
Format: Article
Language:English
Published: BMC 2025-02-01
Series:BMC Pulmonary Medicine
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Online Access:https://doi.org/10.1186/s12890-025-03519-x
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author Lianghui Chen
Yazhen Chen
Fansen Lin
Jianbao Wang
Hongzhi Gao
Yuqi Liu
author_facet Lianghui Chen
Yazhen Chen
Fansen Lin
Jianbao Wang
Hongzhi Gao
Yuqi Liu
author_sort Lianghui Chen
collection DOAJ
description Abstract Background Aspiration pneumonia (AP) is a type of lung inflammation caused by the aspiration of food, oropharyngeal secretions, or gastric contents. This condition is particularly common in older adults and individuals with impaired swallowing or consciousness. While the diagnosis of AP relies on clinical history, swallowing assessments, and imaging, these methods have significant limitations, often leading to underdiagnosis or misdiagnosis. Reliable biomarkers for AP diagnosis are lacking, making early detection and treatment challenging. Methods Nineteen patients diagnosed with pneumonia were included in this study, divided into two groups: AP (n = 10) and non-AP (n = 9). Biological fluid samples, including bronchoalveolar lavage fluid (BALF), saliva, serum, sputum, and urine, were analyzed using non-targeted liquid chromatography with tandem mass spectrometry (LC-MS/MS). Differential metabolites were identified using fold change analysis, statistical significance, and receiver operating characteristic (ROC) curve analysis to evaluate their diagnostic potential. Spearman correlation was used to examine the relationship between selected metabolites and clinical parameters. Results Significant metabolic differences were found between AP and non-AP patients, with many different metabolites identified across biological fluids. Dehydroepiandrosterone sulfate (DHEAS), Androstenediol-3-sulfate (ADIOLS), and beta-muricholic acid were identified as key biomarkers through fold change analysis and ROC curve analysis, showing consistent increasing or decreasing trends in BALF, sputum, and serum samples. DHEAS was found to be negatively correlated with the Acute Physiology and Chronic Health Evaluation II (APACHE II) (r = − 0.619, p = 0.005) in BALF sample. The area under curve (AUC) values showed that these molecules could serve as effective biomarkers for AP. Conclusions This study identifies DHEAS, ADIOLS and beta-muricholic acid as promising biomarkers for AP, with the potential to improve early diagnosis and treatment. These findings underscore the clinical value of metabolomics in developing diagnostic tools for AP, facilitating better clinical management and patient outcomes. Further research is required to validate these biomarkers in larger cohorts and explore their mechanistic roles in AP pathophysiology.
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spelling doaj-art-9ee97051981d4990964bb49962e5d4302025-02-09T12:09:37ZengBMCBMC Pulmonary Medicine1471-24662025-02-0125111310.1186/s12890-025-03519-xStudy on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumoniaLianghui Chen0Yazhen Chen1Fansen Lin2Jianbao Wang3Hongzhi Gao4Yuqi Liu5Department of Critical Care Medicine, Second Affiliated Hospital of Fujian Medical UniversityDepartment of Critical Care Medicine, Second Affiliated Hospital of Fujian Medical UniversityDepartment of Critical Care Medicine, Second Affiliated Hospital of Fujian Medical UniversityDepartment of Critical Care Medicine, Second Affiliated Hospital of Fujian Medical UniversityDepartment of Neurosurgery, Second Affiliated Hospital of Fujian Medical UniversityDepartment of Critical Care Medicine, Second Affiliated Hospital of Fujian Medical UniversityAbstract Background Aspiration pneumonia (AP) is a type of lung inflammation caused by the aspiration of food, oropharyngeal secretions, or gastric contents. This condition is particularly common in older adults and individuals with impaired swallowing or consciousness. While the diagnosis of AP relies on clinical history, swallowing assessments, and imaging, these methods have significant limitations, often leading to underdiagnosis or misdiagnosis. Reliable biomarkers for AP diagnosis are lacking, making early detection and treatment challenging. Methods Nineteen patients diagnosed with pneumonia were included in this study, divided into two groups: AP (n = 10) and non-AP (n = 9). Biological fluid samples, including bronchoalveolar lavage fluid (BALF), saliva, serum, sputum, and urine, were analyzed using non-targeted liquid chromatography with tandem mass spectrometry (LC-MS/MS). Differential metabolites were identified using fold change analysis, statistical significance, and receiver operating characteristic (ROC) curve analysis to evaluate their diagnostic potential. Spearman correlation was used to examine the relationship between selected metabolites and clinical parameters. Results Significant metabolic differences were found between AP and non-AP patients, with many different metabolites identified across biological fluids. Dehydroepiandrosterone sulfate (DHEAS), Androstenediol-3-sulfate (ADIOLS), and beta-muricholic acid were identified as key biomarkers through fold change analysis and ROC curve analysis, showing consistent increasing or decreasing trends in BALF, sputum, and serum samples. DHEAS was found to be negatively correlated with the Acute Physiology and Chronic Health Evaluation II (APACHE II) (r = − 0.619, p = 0.005) in BALF sample. The area under curve (AUC) values showed that these molecules could serve as effective biomarkers for AP. Conclusions This study identifies DHEAS, ADIOLS and beta-muricholic acid as promising biomarkers for AP, with the potential to improve early diagnosis and treatment. These findings underscore the clinical value of metabolomics in developing diagnostic tools for AP, facilitating better clinical management and patient outcomes. Further research is required to validate these biomarkers in larger cohorts and explore their mechanistic roles in AP pathophysiology.https://doi.org/10.1186/s12890-025-03519-xAspiration pneumoniaMetabolic profilesBiomarkerLiquid chromatography with tandem mass spectrometry
spellingShingle Lianghui Chen
Yazhen Chen
Fansen Lin
Jianbao Wang
Hongzhi Gao
Yuqi Liu
Study on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumonia
BMC Pulmonary Medicine
Aspiration pneumonia
Metabolic profiles
Biomarker
Liquid chromatography with tandem mass spectrometry
title Study on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumonia
title_full Study on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumonia
title_fullStr Study on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumonia
title_full_unstemmed Study on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumonia
title_short Study on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumonia
title_sort study on the potential diagnostic value of metabolomics changes in different biological fluids for aspiration pneumonia
topic Aspiration pneumonia
Metabolic profiles
Biomarker
Liquid chromatography with tandem mass spectrometry
url https://doi.org/10.1186/s12890-025-03519-x
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