Key result
Higher serum thrombomodulin is linked to non-pneumonic bacterial infections but fails to identify pneumococcal community-acquired pneumonia.
Why the study?
Soluble thrombomodulin has been proposed as an endothelial injury marker with potential diagnostic value for severe pneumococcal CAP, but its validation for patient stratification and biomarker-guided therapy was needed.
Does serum thrombomodulin level differentiate pneumococcal community-acquired pneumonia from other infections or correlate with disease severity in patients presenting to the emergency department?
Observational (n=80)
No
Does serum thrombomodulin level differentiate pneumococcal community-acquired pneumonia from other infections or correlate with disease severity in patients presenting to the emergency department?
Absolute Event Rate: 7.1% vs 4.1%
p-value: p=<0.0001
Serum thrombomodulin is elevated in non-pneumonic bacterial infections but does not specifically identify pneumococcal community-acquired pneumonia or correlate with its severity.
Serum thrombomodulin should not be used to differentiate or stratify pneumococcal CAP in the ED; leaves open its role in non-pneumonic bacterial infections.
Objective: Soluble thrombomodulin (TM) has been proposed as an endothelial injury marker with potential diagnostic value, particularly for severe pneumococcal community-acquired pneumonia (CAP). Its validation could enable clinically meaningful patient stratification and support biomarker-guided therapy. This retrospective study evaluated the associations between serum TM levels and disease severity/origin in 80 patients with suspected acute infection. Methods: Serum TM concentrations were measured in patients presenting to the emergency department and adjudicated by an expert panel as pneumococcal CAP, non-pneumococcal CAP, other bacterial infections (non-pneumonic), viral pneumonia, or patients with clinically ruled-out infection (controls). Results: TM levels did not differ significantly between CAP patients and controls or those with other bacterial infections. However, highest TM concentrations were observed in patients with bacterial infections without pneumonia, significantly exceeding control levels. TM levels were not correlated with disease severity in CAP, determined by National Early Warning Score 2 (NEWS2), but were significantly elevated in non-pneumonic bacterial infections of moderate severity (NEWS2 5– 6). Conclusion: In this cohort, TM was elevated in bacterial non-pneumonic infections but was not a specific marker for pneumococcal CAP. These findings indicate that TM predominantly reflects systemic endothelial injury, a hallmark of more severe bacterial infections, particularly those of non-pneumonic origin.
No takes yet. Share an insight, caveat, or question.
Friedrich et al. (2026) conducted an observational in Suspected acute infection (n=80). Serum thrombomodulin (TM) measurement vs. Controls (no infection) was evaluated on Serum thrombomodulin concentration (p=<0.0001). Serum thrombomodulin was significantly elevated in non-pneumonic bacterial infections compared to controls, but did not specifically identify pneumococcal community-acquired pneumonia.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: