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Identification of biological correlates associated with respiratory failure in COVID-19

BACKGROUND: Coronavirus disease 2019 (COVID-19) is a global public health concern. Recently, a genome-wide association study (GWAS) was performed with participants recruited from Italy and Spain by an international consortium group. METHODS: Summary GWAS statistics for 1610 patients with COVID-19 re...

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Autores principales: Oh, Jung Hun, Tannenbaum, Allen, Deasy, Joseph O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729705/
https://www.ncbi.nlm.nih.gov/pubmed/33308225
http://dx.doi.org/10.1186/s12920-020-00839-1
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author Oh, Jung Hun
Tannenbaum, Allen
Deasy, Joseph O.
author_facet Oh, Jung Hun
Tannenbaum, Allen
Deasy, Joseph O.
author_sort Oh, Jung Hun
collection PubMed
description BACKGROUND: Coronavirus disease 2019 (COVID-19) is a global public health concern. Recently, a genome-wide association study (GWAS) was performed with participants recruited from Italy and Spain by an international consortium group. METHODS: Summary GWAS statistics for 1610 patients with COVID-19 respiratory failure and 2205 controls were downloaded. In the current study, we analyzed the summary statistics with the information of loci and p-values for 8,582,968 single-nucleotide polymorphisms (SNPs), using gene ontology analysis to determine the top biological processes implicated in respiratory failure in COVID-19 patients. RESULTS: We considered the top 708 SNPs, using a p-value cutoff of 5 × 10(− 5), which were mapped to the nearest genes, leading to 144 unique genes. The list of genes was input into a curated database to conduct gene ontology and protein-protein interaction (PPI) analyses. The top ranked biological processes were wound healing, epithelial structure maintenance, muscle system processes, and cardiac-relevant biological processes with a false discovery rate < 0.05. In the PPI analysis, the largest connected network consisted of 8 genes. Through a literature search, 7 out of the 8 gene products were found to be implicated in both pulmonary and cardiac diseases. CONCLUSION: Gene ontology and PPI analyses identified cardio-pulmonary processes that may partially explain the risk of respiratory failure in COVID-19 patients.
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spelling pubmed-77297052020-12-11 Identification of biological correlates associated with respiratory failure in COVID-19 Oh, Jung Hun Tannenbaum, Allen Deasy, Joseph O. BMC Med Genomics Research Article BACKGROUND: Coronavirus disease 2019 (COVID-19) is a global public health concern. Recently, a genome-wide association study (GWAS) was performed with participants recruited from Italy and Spain by an international consortium group. METHODS: Summary GWAS statistics for 1610 patients with COVID-19 respiratory failure and 2205 controls were downloaded. In the current study, we analyzed the summary statistics with the information of loci and p-values for 8,582,968 single-nucleotide polymorphisms (SNPs), using gene ontology analysis to determine the top biological processes implicated in respiratory failure in COVID-19 patients. RESULTS: We considered the top 708 SNPs, using a p-value cutoff of 5 × 10(− 5), which were mapped to the nearest genes, leading to 144 unique genes. The list of genes was input into a curated database to conduct gene ontology and protein-protein interaction (PPI) analyses. The top ranked biological processes were wound healing, epithelial structure maintenance, muscle system processes, and cardiac-relevant biological processes with a false discovery rate < 0.05. In the PPI analysis, the largest connected network consisted of 8 genes. Through a literature search, 7 out of the 8 gene products were found to be implicated in both pulmonary and cardiac diseases. CONCLUSION: Gene ontology and PPI analyses identified cardio-pulmonary processes that may partially explain the risk of respiratory failure in COVID-19 patients. BioMed Central 2020-12-11 /pmc/articles/PMC7729705/ /pubmed/33308225 http://dx.doi.org/10.1186/s12920-020-00839-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Oh, Jung Hun
Tannenbaum, Allen
Deasy, Joseph O.
Identification of biological correlates associated with respiratory failure in COVID-19
title Identification of biological correlates associated with respiratory failure in COVID-19
title_full Identification of biological correlates associated with respiratory failure in COVID-19
title_fullStr Identification of biological correlates associated with respiratory failure in COVID-19
title_full_unstemmed Identification of biological correlates associated with respiratory failure in COVID-19
title_short Identification of biological correlates associated with respiratory failure in COVID-19
title_sort identification of biological correlates associated with respiratory failure in covid-19
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729705/
https://www.ncbi.nlm.nih.gov/pubmed/33308225
http://dx.doi.org/10.1186/s12920-020-00839-1
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