Evidence map›Paper›PMID 39283042›Full record

ArticleAnnals of medicine2024

Serum metabolomics profile identifies patients with community-acquired pneumonia infected by bacteria, fungi, and viruses.

Li Chen, Jianbo Xue, Yukun He, Lili Zhao, Ying Zhang, Lu Yin, Shining Fu, Wenyi Yu, Xinqian Ma, Yu Wang and 2 more

Abstract read
In one paragraph

Article in Annals of medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Metabolomic analysis ofFrontiers in microbiology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Li ChenDepartment of Respiratory, Beijing Ditan Hospital, Capital Medical University, Beijing, People's Republic of China.
Jianbo XueDepartment of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Yukun HeDepartment of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Lili ZhaoDepartment of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Ying ZhangDepartment of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Lu YinDepartment of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Shining FuDepartment of Respiratory and Critical Care Medicine, Beijing Jishuitan Hospital, Beijing, China.
Wenyi YuDepartment of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Xinqian MaDepartment of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Yu WangDepartment of Respiratory, Beijing Ditan Hospital, Capital Medical University, Beijing, People's Republic of China.
Yanfen TangDepartment of Respiratory, Beijing Ditan Hospital, Capital Medical University, Beijing, People's Republic of China.
Zhancheng GaoDepartment of Respiratory & Critical Care Medicine, Peking University People's Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePatients with bacterial, fungal, and viral community-acquired pneumonia (CAP) were studied to determine their metabolic profiles.

methodsLoop-mediated isothermal amplification technology and nucleic acid sequence-dependent amplification combined with microfluidic chip technology were applied to screen multiple pathogens from respiratory tract samples. Eighteen patients with single bacterial infection (B-CAP), fifteen with single virus infection (V-CAP), twenty with single fungal infection (F-CAP), and twenty controls were enrolled. UHPLC-MS/MS analysis of untargeted serum samples for metabolic profiles. Multiple linear regression and Spearman's rank correlation analysis were used to determine associations between metabolites and clinical parameters. The sensitivity and specificity of the screened metabolites were also examined, along with their area under the curve.

resultsThe metabolic signatures of patients with CAP infected by bacteria, viruses, and fungi were markedly different from those of controls. The abundances of 45, 56, and 79 metabolites were significantly unbalanced. Among these differential metabolites, 11, 13, and 29 were unique to the B-CAP, V-CAP, and F-CAP groups, respectively. Bacterial infections were the only known causes of disturbances in the pentose and glucuronate and aldarate and ascorbate metabolism interconversions metabolic pathway.

conclusionsSerum metabolomic techniques based on UHPLC-MS/MS may identify differences between individuals with CAP who have been infected by various pathogens, and they can also build a metabolite signature for early detection of the origin of infection and prompt care.

Indexed as

Community-Acquired InfectionsMetabolomicsAdultAgedCase-Control StudiesChromatography, High Pressure LiquidFemaleHumansMaleMetabolomeMiddle AgedPneumonia, BacterialPneumonia, ViralSensitivity and SpecificityTandem Mass Spectrometrybacterial infectioncommunity-acquired pneumoniadiagnosisfungal infectionMetabolomics profilesviral infection

Identifiers

PMID39283042
PMCPMC11407381

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