AI Article Synopsis

  • The COVID-19 pandemic has challenged global healthcare systems, prompting research into genetic and proteomic markers for better patient prognosis.
  • A study analyzed the protein and genetic profiles of 400 hospitalized and 483 non-hospitalized COVID-19 patients, uncovering 224 proteins linked to inflammation and immunity.
  • Key proteins like LGALS9 and LAMP3 were identified as significant predictors of severe illness, suggesting these markers could serve as important tools for understanding and treating COVID-19 outcomes.

Article Abstract

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. 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). 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 (-value < 0.001), LAMP3 (-value < 0.001), PRSS8 (-value < 0.001) and AGRN (-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 gene showing a correlation with hospitalisation status. 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11429560PMC
http://dx.doi.org/10.3390/biom14091163DOI Listing

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