# Biomarker studies to predict outcomes of patients with COVID-19 related acute respiratory distress syndrome measured pre and post initiation of veno venous extracorporeal membrane oxygenation

**Authors:** Mazen F. Odish, Hunter Gage, Michael T. Y. Lam, Mark Hepokoski, Travis Pollema, Khang Tong, Lin Liu, Atul Malhotra, Robert L. Owens, Angela Meier

PMC · DOI: 10.1038/s41598-025-30047-9 · 2025-12-03

## TL;DR

The study investigates whether biomarker levels before ECMO treatment can predict survival in patients with severe COVID-19-related lung failure.

## Contribution

The study evaluates the predictive value of IL-10 and other biomarkers for survival in patients with COVID-19 ARDS undergoing ECMO.

## Key findings

- IL-10 levels before ECMO initiation did not predict survival in patients with COVID-19 ARDS.
- Other biomarkers like Ang 1, TNF-alpha, Mitochondrial DNA, and IP-10 showed significant differences between survivors and non-survivors.
- AUC analysis confirmed that IL-10 was not a reliable predictor of survival in this patient group.

## Abstract

Veno-venous extracorporeal membrane oxygenation (V-V ECMO) is a resource intensive and expensive therapy increasingly used to treat a select group of patients with severe acute respiratory distress syndrome (ARDS). High levels of Interleukin-10 (IL-10) are reported to be predictive of mortality in non-COVID ARDS patients receiving ECMO. In this study we evaluated if levels of biomarkers including IL-10 can predict mortality if measured prior to ECMO initiation in patients with COVID-19 ARDS. A total of sixteen patients with COVID-related ARDS undergoing treatment with ECMO were included in the pre-ECMO biomarker analysis, while samples from a total of 22 patients with post-ECMO samples were analyzed. Nine of sixteen patients with pre-ECMO samples (56%) survived to hospital discharge. There was no difference in baseline demographics between survivors and non-survivors. In univariate analysis, survivors had no difference in IL-10 levels prior to ECMO initiation although we identified several other biomarkers (Ang 1 and TNF-alpha with logistical regression, Mitochondrial DNA and IP-10 with Kaplan–Meier analysis) that differed significantly between survivors and non-survivors. Moreover, as opposed to a prior study, area under the curve (AUC) analysis showed that IL-10 levels were not predictive of survival. We advise caution for utilizing a single biomarker as outcome predictor in this highly complex population with often long clinical courses despite our promising results.

The online version contains supplementary material available at 10.1038/s41598-025-30047-9.

## Linked entities

- **Proteins:** IL10 (interleukin 10), ANGPT1 (angiopoietin 1), TNF (tumor necrosis factor), CXCL10 (C-X-C motif chemokine ligand 10)
- **Diseases:** acute respiratory distress syndrome (MONDO:0006502), ARDS (MONDO:0006502), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, ANGPT1 (angiopoietin 1) [NCBI Gene 284] {aka AGP1, AGPT, AGPT-1, ANG1, HAE5}
- **Diseases:** COVID (MESH:D000086382), severe acute respiratory distress syndrome (MESH:D045169), ARDS (MESH:D012128)
- **Chemicals:** extracorporeal membrane (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12775480/full.md

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Source: https://tomesphere.com/paper/PMC12775480