Serum expression of ESM-1 and Syndecan-1 and its relationship with disease severity in children with Mycoplasma pneumoniae pneumonia
- PMID: 40764585
- PMCID: PMC12326627
- DOI: 10.1186/s13052-025-02105-5
Serum expression of ESM-1 and Syndecan-1 and its relationship with disease severity in children with Mycoplasma pneumoniae pneumonia
Abstract
Background: This study aim to investigate the role of endothelial damage in the pathogenesis of Mycoplasma pneumoniae pneumonia (MPP) by comparing serum levels of endothelial cell-specific molecule 1 (ESM-1) and Syndecan-1 in patients with varying degrees of MPP severity. Additionally, we aim to explore the relationship between the production of ESM-1 and Syndecan-1 and the severity of MPP, inflammation, as well as hypercoagulative state in children.
Methods: A prospective, observational study that included clinical manifestations, laboratory tests, and serum ESM-1 and Syndecan-1 assays. The correlation between ESM-1 and Syndecan-1 levels with inflammatory markers and coagulation markers was analyzed. Multivariate logistic regression analysis was conducted to identify significant risk factors for Severe Mycoplasma pneumoniae pneumonia (SMPP).
Results: A total of 179 children with MPP and 40 healthy volunteers were enrolled. Serum ESM-1 and Syndecan-1 levels were significantly elevated in children with MPP compared to the healthy children (all P < 0.05). A multivariate analysis revealed that ESM-1, Syndecan-1, D-dimer and LDH were the significant predictors of SMPP, with odds ratios of 1.034, 1.002, 5.042 and 1.014, respectively. The optimal cutoff values of ESM-1, Syndecan-1, D-dimer and LDH for predicting SMPP were 79.67 ng/mL, 3219.35 pg/mL, 0.67 µg/mL and 365.00 U/L, respectively.
Conclusions: ESM-1, Syndecan-1, D-dimer, and LDH can serve as independent predictors for SMPP. The interaction between endothelial damage, excessive inflammatory response, and hypercoagulable state collectively contributes to the development and progression of SMPP.
Keywords: ESM-1; Endothelial damage; Independent predictors; Severe Mycoplasma pneumoniae pneumonia; Syndecan-1.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval: The study was approved by the Ethics Committee of Children’s Hospital Affiliated to Zhengzhou University (Approval no. 2024-K-065). In addition, informed consent was obtained from the patients for the publication of all clinical data included in the main manuscript. Consent for publication: Written informed consent for publication was obtained from all participants. Conflict of interest: The authors have no conflicts of interest to disclose.
Figures


Similar articles
-
The predictive value of MUC5AC levels in the sputum of children with Mycoplasma pneumoniae pneumonia treated with fiberbronchoscopy.Microbiol Spectr. 2025 Aug 5;13(8):e0010325. doi: 10.1128/spectrum.00103-25. Epub 2025 Jul 2. Microbiol Spectr. 2025. PMID: 40600698 Free PMC article.
-
Assessment of serum parameters caused by the outbreak of mycoplasma pneumoniae pneumonia in children after COVID-19.Sci Rep. 2025 Aug 3;15(1):28306. doi: 10.1038/s41598-025-13555-6. Sci Rep. 2025. PMID: 40754552 Free PMC article.
-
Multi-omics analysis of human plasma reveals reprogramming of tryptophan metabolism associated with inflammation in Mycoplasma pneumoniae pneumonia in children.J Infect. 2025 Jul;91(1):106525. doi: 10.1016/j.jinf.2025.106525. Epub 2025 May 31. J Infect. 2025. PMID: 40456320
-
Clinical symptoms and signs for the diagnosis of Mycoplasma pneumoniae in children and adolescents with community-acquired pneumonia.Cochrane Database Syst Rev. 2012 Oct 17;10(10):CD009175. doi: 10.1002/14651858.CD009175.pub2. Cochrane Database Syst Rev. 2012. PMID: 23076954 Free PMC article.
-
Accuracy of routine laboratory tests to predict mortality and deterioration to severe or critical COVID-19 in people with SARS-CoV-2.Cochrane Database Syst Rev. 2024 Aug 6;8(8):CD015050. doi: 10.1002/14651858.CD015050.pub2. Cochrane Database Syst Rev. 2024. PMID: 39105481 Free PMC article.
References
-
- ESGMAC MAPS study group. Global Spatiotemporal dynamics of Mycoplasma pneumoniae re-emergence after COVID-19 pandemic restrictions: an epidemiological and transmission modelling study. Lancet Microbe. 2025;6(4):101019. 10.1016/j.lanmic.2024.101019. - PubMed
-
- Li H, Li S, Yang H, Chen Z. Zhemin zhou; resurgence of Mycoplasma pneumonia by macrolide-resistant epidemic clones in China. Lancet Microbe. 2024;5(6):e515. 10.1016/S2666-5247(23)00405-6. - PubMed
-
- World Health Organization. Upsurge of respiratory illnesses among children in northern China[EB/OL]. (2023-11-23) [2024-03-01]. https://www.who.int/emergencies/diseaseoutbreaknews/item/2023DON494.
-
- Luo XQ, Luo J, Wang CJ, et al. Clinical features of severe Mycoplasma pneumoniae pneumonia with pulmonary complications in childhood: A retrospective study. Pediatr Pulmonol. 2023;10(10):2815–22. 10.1002/ppul.26593. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous