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Gene Expression Risk Scores for COVID-19 Illness Severity
BACKGROUND: The correlates of coronavirus disease 2019 (COVID-19) illness severity following infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are incompletely understood. METHODS: We assessed peripheral blood gene expression in 53 adults with confirmed SARS-CoV-2 infection...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767880/ https://www.ncbi.nlm.nih.gov/pubmed/34850892 http://dx.doi.org/10.1093/infdis/jiab568 |
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author | Peterson, Derick R Baran, Andrea M Bhattacharya, Soumyaroop Branche, Angela R Croft, Daniel P Corbett, Anthony M Walsh, Edward E Falsey, Ann R Mariani, Thomas J |
author_facet | Peterson, Derick R Baran, Andrea M Bhattacharya, Soumyaroop Branche, Angela R Croft, Daniel P Corbett, Anthony M Walsh, Edward E Falsey, Ann R Mariani, Thomas J |
author_sort | Peterson, Derick R |
collection | PubMed |
description | BACKGROUND: The correlates of coronavirus disease 2019 (COVID-19) illness severity following infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are incompletely understood. METHODS: We assessed peripheral blood gene expression in 53 adults with confirmed SARS-CoV-2 infection clinically adjudicated as having mild, moderate, or severe disease. Supervised principal components analysis was used to build a weighted gene expression risk score (WGERS) to discriminate between severe and nonsevere COVID-19. RESULTS: Gene expression patterns in participants with mild and moderate illness were similar, but significantly different from severe illness. When comparing severe versus nonsevere illness, we identified >4000 genes differentially expressed (false discovery rate < 0.05). Biological pathways increased in severe COVID-19 were associated with platelet activation and coagulation, and those significantly decreased with T-cell signaling and differentiation. A WGERS based on 18 genes distinguished severe illness in our training cohort (cross-validated receiver operating characteristic-area under the curve [ROC-AUC] = 0.98), and need for intensive care in an independent cohort (ROC-AUC = 0.85). Dichotomizing the WGERS yielded 100% sensitivity and 85% specificity for classifying severe illness in our training cohort, and 84% sensitivity and 74% specificity for defining the need for intensive care in the validation cohort. CONCLUSIONS: These data suggest that gene expression classifiers may provide clinical utility as predictors of COVID-19 illness severity. |
format | Online Article Text |
id | pubmed-8767880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87678802022-01-20 Gene Expression Risk Scores for COVID-19 Illness Severity Peterson, Derick R Baran, Andrea M Bhattacharya, Soumyaroop Branche, Angela R Croft, Daniel P Corbett, Anthony M Walsh, Edward E Falsey, Ann R Mariani, Thomas J J Infect Dis Major Article BACKGROUND: The correlates of coronavirus disease 2019 (COVID-19) illness severity following infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are incompletely understood. METHODS: We assessed peripheral blood gene expression in 53 adults with confirmed SARS-CoV-2 infection clinically adjudicated as having mild, moderate, or severe disease. Supervised principal components analysis was used to build a weighted gene expression risk score (WGERS) to discriminate between severe and nonsevere COVID-19. RESULTS: Gene expression patterns in participants with mild and moderate illness were similar, but significantly different from severe illness. When comparing severe versus nonsevere illness, we identified >4000 genes differentially expressed (false discovery rate < 0.05). Biological pathways increased in severe COVID-19 were associated with platelet activation and coagulation, and those significantly decreased with T-cell signaling and differentiation. A WGERS based on 18 genes distinguished severe illness in our training cohort (cross-validated receiver operating characteristic-area under the curve [ROC-AUC] = 0.98), and need for intensive care in an independent cohort (ROC-AUC = 0.85). Dichotomizing the WGERS yielded 100% sensitivity and 85% specificity for classifying severe illness in our training cohort, and 84% sensitivity and 74% specificity for defining the need for intensive care in the validation cohort. CONCLUSIONS: These data suggest that gene expression classifiers may provide clinical utility as predictors of COVID-19 illness severity. Oxford University Press 2021-11-30 /pmc/articles/PMC8767880/ /pubmed/34850892 http://dx.doi.org/10.1093/infdis/jiab568 Text en © The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. https://academic.oup.com/pages/standard-publication-reuse-rightsThis article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model) |
spellingShingle | Major Article Peterson, Derick R Baran, Andrea M Bhattacharya, Soumyaroop Branche, Angela R Croft, Daniel P Corbett, Anthony M Walsh, Edward E Falsey, Ann R Mariani, Thomas J Gene Expression Risk Scores for COVID-19 Illness Severity |
title | Gene Expression Risk Scores for COVID-19 Illness Severity |
title_full | Gene Expression Risk Scores for COVID-19 Illness Severity |
title_fullStr | Gene Expression Risk Scores for COVID-19 Illness Severity |
title_full_unstemmed | Gene Expression Risk Scores for COVID-19 Illness Severity |
title_short | Gene Expression Risk Scores for COVID-19 Illness Severity |
title_sort | gene expression risk scores for covid-19 illness severity |
topic | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767880/ https://www.ncbi.nlm.nih.gov/pubmed/34850892 http://dx.doi.org/10.1093/infdis/jiab568 |
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