Precision medicine for pandemics: stratification of COVID-19 molecular phenotypes defined by topological analysis of global blood gene expression.
Precision medicine for pandemics: stratification of COVID-19 molecular phenotypes defined by topological analysis of global blood gene expression.
Precision medicine offers a promising avenue for better therapeutic responses to pandemics such as COVID-19. This study leverages independent patient cohorts in Florence and Liège gathered under the umbrella of the DRAGON consortium for the stratification of molecular phenotypes associated with COVID-19 using topological analysis of global blood gene expression. Whole blood from 173 patients was collected and RNA was sequenced on the Novaseq platform. Molecular phenotypes were defined through topological analysis of gene expression relative to the biological network using the TopMD algorithm. The two cohorts from Florence and Liège allowed for independent validation of the findings in this study. Clustering of the topological maps of differential pathway activation revealed three distinct molecular phenotypes of COVID-19 in the Florence patient cohort, which were also observed in the Liège cohort.
Cluster 1 was characterised by high activation of pathways associated with ESC pluripotency, NRF2, and TGF-β receptor signalling. Cluster 2 displayed high activation of pathways including focal adhesion-PI3K-Akt-mTOR signalling and type I interferon induction and signalling, while Cluster 3 exhibited low IRF7-related pathway activation. TopMD was also used with the Drug-Gene Interaction Database (DGIdb), revealing pharmaceutical interventions targeting mechanisms across multiple phenotypes and individuals.
The data illustrates the utility of molecular phenotyping from topological analysis of blood gene expression, and holds promise for informing personalised therapeutic strategies not only for COVID-19 but also for Disease X. Its potential transferability across multiple diseases highlights the value in pandemic response efforts, offering insights before large-scale clinical studies are initiated.
COVID-19, TopMD, topological data analysis, molecular phenotyping
Penrice-Randal, Rebekah
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Strazzeri, Fabio
bd80afa2-b453-4ae8-9de2-0de540f48445
Ernst, Benoit
be53a934-1380-451c-8933-9bf29ab8231a
Skipp, Paul
1ba7dcf6-9fe7-4b5c-a9d0-e32ed7f42aa5
15 April 2024
Penrice-Randal, Rebekah
5cdbce6b-4d9b-46b0-b9b0-27657d78e021
Strazzeri, Fabio
bd80afa2-b453-4ae8-9de2-0de540f48445
Ernst, Benoit
be53a934-1380-451c-8933-9bf29ab8231a
Skipp, Paul
1ba7dcf6-9fe7-4b5c-a9d0-e32ed7f42aa5
[Unknown type: UNSPECIFIED]
Abstract
Precision medicine offers a promising avenue for better therapeutic responses to pandemics such as COVID-19. This study leverages independent patient cohorts in Florence and Liège gathered under the umbrella of the DRAGON consortium for the stratification of molecular phenotypes associated with COVID-19 using topological analysis of global blood gene expression. Whole blood from 173 patients was collected and RNA was sequenced on the Novaseq platform. Molecular phenotypes were defined through topological analysis of gene expression relative to the biological network using the TopMD algorithm. The two cohorts from Florence and Liège allowed for independent validation of the findings in this study. Clustering of the topological maps of differential pathway activation revealed three distinct molecular phenotypes of COVID-19 in the Florence patient cohort, which were also observed in the Liège cohort.
Cluster 1 was characterised by high activation of pathways associated with ESC pluripotency, NRF2, and TGF-β receptor signalling. Cluster 2 displayed high activation of pathways including focal adhesion-PI3K-Akt-mTOR signalling and type I interferon induction and signalling, while Cluster 3 exhibited low IRF7-related pathway activation. TopMD was also used with the Drug-Gene Interaction Database (DGIdb), revealing pharmaceutical interventions targeting mechanisms across multiple phenotypes and individuals.
The data illustrates the utility of molecular phenotyping from topological analysis of blood gene expression, and holds promise for informing personalised therapeutic strategies not only for COVID-19 but also for Disease X. Its potential transferability across multiple diseases highlights the value in pandemic response efforts, offering insights before large-scale clinical studies are initiated.
Text
2024.04.15.24305820v1.full
- Author's Original
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Published date: 15 April 2024
Keywords:
COVID-19, TopMD, topological data analysis, molecular phenotyping
Identifiers
Local EPrints ID: 491336
URI: http://eprints.soton.ac.uk/id/eprint/491336
PURE UUID: 50767252-9e81-421b-9e58-d2de33708634
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Date deposited: 20 Jun 2024 16:34
Last modified: 21 Jun 2024 01:33
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Contributors
Author:
Rebekah Penrice-Randal
Author:
Fabio Strazzeri
Author:
Benoit Ernst
Corporate Author: et al.
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