Abstract
Background: The COVID-19 pandemic, caused by the novel coronavirus SARS-CoV-2, has posed unprecedented challenges to healthcare systems worldwide. Here, we have identified proteomic and genetic signatures for improved prognosis which is vital for COVID-19 research. Methods: We investigated the proteomic and genomic profile of COVID-19-positive patients (n = 400 for proteomics, n = 483 for genomics), focusing on differential regulation between hospitalised and non-hospitalised COVID-19 patients. Signatures had their predictive capabilities tested using independent machine learning models such as Support Vector Machine (SVM), Random Forest (RF) and Logistic Regression (LR). Results: This study has identified 224 differentially expressed proteins involved in various inflammatory and immunological pathways in hospitalised COVID-19 patients compared to non-hospitalised COVID-19 patients. LGALS9 (p-value < 0.001), LAMP3 (p-value < 0.001), PRSS8 (p-value < 0.001) and AGRN (p-value < 0.001) were identified as the most statistically significant proteins. Several hundred rsIDs were queried across the top 10 significant signatures, identifying three significant SNPs on the FSTL3 gene showing a correlation with hospitalisation status. Conclusions: Our study has not only identified key signatures of COVID-19 patients with worsened health but has also demonstrated their predictive capabilities as potential biomarkers, which suggests a staple role in the worsened health effects caused by COVID-19.
Original language | English |
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Article number | 1163 |
Pages (from-to) | 1-17 |
Number of pages | 17 |
Journal | Biomolecules |
Volume | 14 |
Issue number | 9 |
Early online date | 17 Sept 2024 |
DOIs | |
Publication status | Published online - 17 Sept 2024 |
Bibliographical note
Publisher Copyright:© 2024 by the authors.
Data Access Statement
The raw data supporting the conclusions of this article will be made available by the authors on request.Keywords
- AGRN
- COVID-19
- LAMP3
- LGALS9
- Logistic Regression
- PRSS8
- Random Forest
- SARS-CoV-2
- Support Vector Machine
- biomarker