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 |
|---|---|
| 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 Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors on request.Funding
This research was funded by the Department for the Economy Northern Ireland research grant under its contribution to Science Foundation Ireland’s COVID-19 Rapid Response Call (Phase 2) to A.J.B., the PHA/HSC R&D Division (COM/5618/20) and the Western Health & Social Care Trust research grants to T.S.R., and Opportunity-Led Research Award to DSG from HSC R&D Division, Public Health Agency (COM/5631/20).
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- AGRN
- COVID-19
- LAMP3
- LGALS9
- Logistic Regression
- PRSS8
- Random Forest
- SARS-CoV-2
- Support Vector Machine
- biomarker
Fingerprint
Dive into the research topics of 'Potential Plasma Proteins (LGALS9, LAMP3, PRSS8 and AGRN) as Predictors of Hospitalisation Risk in COVID-19 Patients'. Together they form a unique fingerprint.Research output
- 3 Citations
- 1 Preprint
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LGALS9, LAMP3, PRSS8 and AGRN Predict Hospitalisation Risk in COVID-19 Patients
McLarnon, T., McDaid, D., Lynch, S. M., Cooper, E., McLaughlin, J., McGilligan, V. E., Watterson, S., Shukla, P., Zhang, S.-D., Bucholc, M., English, A., Peace, A., O'Kane, M., Kelly, M., Bhavsar, M., Murray, E. K., Gibson, D. S., Walsh, C. P., Bjourson, A. J. & Rai, T. S., 26 Aug 2024, (Published online) p. 1-19, 19 p.Research output: Working paper › Preprint
Student theses
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A multi-omics analysis of age-associated diseases to identify novel sendotypes
McLarnon, T. (Author), Watterson, S. (Supervisor), Zhang, S.-D. (Supervisor), Rai, T. S. (Supervisor) & Gibson, D. (Supervisor), Feb 2026Student thesis: Doctoral Thesis
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