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Potential Plasma Proteins (LGALS9, LAMP3, PRSS8 and AGRN) as Predictors of Hospitalisation Risk in COVID-19 Patients.
McLarnon, Thomas; McDaid, Darren; Lynch, Seodhna M; Cooper, Eamonn; McLaughlin, Joseph; McGilligan, Victoria E; Watterson, Steven; Shukla, Priyank; Zhang, Shu-Dong; Bucholc, Magda; English, Andrew; Peace, Aaron; O'Kane, Maurice; Kelly, Martin; Bhavsar, Manav; Murray, Elaine K; Gibson, David S; Walsh, Colum P; Bjourson, Anthony J; Rai, Taranjit Singh.
Afiliação
  • McLarnon T; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • McDaid D; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Lynch SM; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Cooper E; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • McLaughlin J; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • McGilligan VE; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Watterson S; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Shukla P; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Zhang SD; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Bucholc M; School of Computing, Engineering & Intelligent Systems, Ulster University, Derry BT48 7JL, UK.
  • English A; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Peace A; School of Health and Life Sciences, Teesside University, Campus Heart, Middlesbrough TS1 3BX, UK.
  • O'Kane M; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Kelly M; Altnagelvin Area Hospital, Western Health and Social Care Trust, Derry BT47 6SB, UK.
  • Bhavsar M; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Murray EK; Clinical Chemistry Laboratory, Altnagelvin Hospital, Derry BT47 6SB, UK.
  • Gibson DS; Altnagelvin Area Hospital, Western Health and Social Care Trust, Derry BT47 6SB, UK.
  • Walsh CP; Altnagelvin Area Hospital, Western Health and Social Care Trust, Derry BT47 6SB, UK.
  • Bjourson AJ; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
  • Rai TS; Personalised Medicine Centre, C-TRIC Building, Altnagelvin Area Hospital, School of Medicine, Ulster University, Glenshane Road, Derry-Londonderry BT47 6SB, UK.
Biomolecules ; 14(9)2024 Sep 17.
Article em En | MEDLINE | ID: mdl-39334929
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Sanguíneas / SARS-CoV-2 / COVID-19 / Hospitalização Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Biomolecules Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Sanguíneas / SARS-CoV-2 / COVID-19 / Hospitalização Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Biomolecules Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido