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Potential Plasma Proteins (LGALS9, LAMP3, PRSS8 and AGRN) as Predictors of Hospitalisation Risk in COVID-19 Patients

Authors :
Thomas McLarnon
Darren McDaid
Seodhna M. Lynch
Eamonn Cooper
Joseph McLaughlin
Victoria E. McGilligan
Steven Watterson
Priyank Shukla
Shu-Dong Zhang
Magda Bucholc
Andrew English
Aaron Peace
Maurice O’Kane
Martin Kelly
Manav Bhavsar
Elaine K. Murray
David S. Gibson
Colum P. Walsh
Anthony J. Bjourson
Taranjit Singh Rai
Source :
Biomolecules, Vol 14, Iss 9, p 1163 (2024)
Publication Year :
2024
Publisher :
MDPI AG, 2024.

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.

Details

Language :
English
ISSN :
2218273X
Volume :
14
Issue :
9
Database :
Directory of Open Access Journals
Journal :
Biomolecules
Publication Type :
Academic Journal
Accession number :
edsdoj.95186f387314385a041feae228bb7a7
Document Type :
article
Full Text :
https://doi.org/10.3390/biom14091163