# Evaluation of suPAR as a Key Prognostic Biomarker in Patients with SARS-CoV-2 Pneumonia

**Authors:** Mónica Piqueras, Paula González-Jiménez, Ana Latorre, Jordi Tortosa-Carreres, Noé Mengot, Ricardo Alonso, Soledad Reyes, Isabel Amara-Elori, Francisco Sanz-Herrero, Rosario Menéndez, Raúl Méndez

PMC · DOI: 10.3390/biomedicines13040896 · Biomedicines · 2025-04-08

## TL;DR

This study shows that the suPAR biomarker can better predict severe outcomes in patients with SARS-CoV-2 pneumonia compared to existing tools.

## Contribution

The study demonstrates that combining suPAR with the CURB-65 score improves risk stratification for patients with SARS-CoV-2 pneumonia.

## Key findings

- suPAR outperformed lymphocyte count and CURB-65 in predicting ICU admission.
- No patient with suPAR < 4 ng/mL experienced severe outcomes.
- Combining suPAR with CURB-65 significantly improved risk classification.

## Abstract

Background/Objectives: SARS-CoV-2 has strained healthcare systems, emphasizing the need for biomarkers to predict disease severity. Recent studies suggest that soluble urokinase plasminogen activator receptor (suPAR) is a promising marker for COVID-19 pneumonia, though its utility alongside the CURB-65 score remains unstudied. This study evaluates the prognostic value of suPAR in comparison to leukocyte count and CURB-65, and its potential for enhancing risk stratification in a combined CURB-65 model. Methods: Biomarkers and CURB-65 scores were obtained for 240 immunocompetent patients hospitalised with COVID-19 pneumonia. Intensive care unit admission and in-hospital mortality were assessed using receiver operating characteristic (ROC) curves and Kaplan–Meier analysis. Additionally, a Net Reclassification Improvement (NRI) analysis was performed to evaluate the predictive value of suPAR combined with the CURB-65 score for risk stratification. Results: suPAR demonstrated strong diagnostic accuracy, outperforming lymphocyte count and showing greater precision than the CURB-65 score for ICU admission. Notably, no patient with suPAR < 4 ng/mL experienced the studied outcomes. NRI analysis revealed a significant improvement in risk classification when suPAR was combined with CURB-65. Conclusions: The addition of the suPAR biomarker to the CURB-65 score represents a substantial improvement in the risk classification of patients with COVID-19 pneumonia, with a potential impact on daily clinical practice.

## Linked entities

- **Proteins:** Su(par) (Suppressor of paralog)

## Full-text entities

- **Genes:** PLAUR (plasminogen activator, urokinase receptor) [NCBI Gene 5329] {aka CD87, U-PAR, UPAR, URKR}
- **Diseases:** COVID-19 pneumonia (MESH:D000086382)
- **Chemicals:** CURB-65 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12024740/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12024740/full.md

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Source: https://tomesphere.com/paper/PMC12024740