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COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases

Epidemiological studies suggest that individuals with comorbid conditions including diabetes, chronic lung, inflammatory and vascular disease, are at higher risk of adverse COVID-19 outcomes. Genome-wide association studies have identified several loci associated with increased susceptibility and se...

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Autores principales: Papadopoulou, Areti, Musa, Hanan, Sivaganesan, Mathura, McCoy, David, Deloukas, Panos, Marouli, Eirini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415605/
https://www.ncbi.nlm.nih.gov/pubmed/34478452
http://dx.doi.org/10.1371/journal.pone.0256988
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author Papadopoulou, Areti
Musa, Hanan
Sivaganesan, Mathura
McCoy, David
Deloukas, Panos
Marouli, Eirini
author_facet Papadopoulou, Areti
Musa, Hanan
Sivaganesan, Mathura
McCoy, David
Deloukas, Panos
Marouli, Eirini
author_sort Papadopoulou, Areti
collection PubMed
description Epidemiological studies suggest that individuals with comorbid conditions including diabetes, chronic lung, inflammatory and vascular disease, are at higher risk of adverse COVID-19 outcomes. Genome-wide association studies have identified several loci associated with increased susceptibility and severity for COVID-19. However, it is not clear whether these associations are genetically determined or not. We used a Phenome-Wide Association (PheWAS) approach to investigate the role of genetically determined COVID-19 susceptibility on disease related outcomes. PheWAS analyses were performed in order to identify traits and diseases related to COVID-19 susceptibility and severity, evaluated through a predictive COVID-19 risk score. We utilised phenotypic data in up to 400,000 individuals from the UK Biobank, including Hospital Episode Statistics and General Practice data. We identified a spectrum of associations between both genetically determined COVID-19 susceptibility and severity with a number of traits. COVID-19 risk was associated with increased risk for phlebitis and thrombophlebitis (OR = 1.11, p = 5.36e(-08)). We also identified significant signals between COVID-19 susceptibility with blood clots in the leg (OR = 1.1, p = 1.66e(-16)) and with increased risk for blood clots in the lung (OR = 1.12, p = 1.45 e(-10)). Our study identifies significant association of genetically determined COVID-19 with increased blood clot events in leg and lungs. The reported associations between both COVID-19 susceptibility and severity and other diseases adds to the identification and stratification of individuals at increased risk, adverse outcomes and long-term effects.
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spelling pubmed-84156052021-09-04 COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases Papadopoulou, Areti Musa, Hanan Sivaganesan, Mathura McCoy, David Deloukas, Panos Marouli, Eirini PLoS One Research Article Epidemiological studies suggest that individuals with comorbid conditions including diabetes, chronic lung, inflammatory and vascular disease, are at higher risk of adverse COVID-19 outcomes. Genome-wide association studies have identified several loci associated with increased susceptibility and severity for COVID-19. However, it is not clear whether these associations are genetically determined or not. We used a Phenome-Wide Association (PheWAS) approach to investigate the role of genetically determined COVID-19 susceptibility on disease related outcomes. PheWAS analyses were performed in order to identify traits and diseases related to COVID-19 susceptibility and severity, evaluated through a predictive COVID-19 risk score. We utilised phenotypic data in up to 400,000 individuals from the UK Biobank, including Hospital Episode Statistics and General Practice data. We identified a spectrum of associations between both genetically determined COVID-19 susceptibility and severity with a number of traits. COVID-19 risk was associated with increased risk for phlebitis and thrombophlebitis (OR = 1.11, p = 5.36e(-08)). We also identified significant signals between COVID-19 susceptibility with blood clots in the leg (OR = 1.1, p = 1.66e(-16)) and with increased risk for blood clots in the lung (OR = 1.12, p = 1.45 e(-10)). Our study identifies significant association of genetically determined COVID-19 with increased blood clot events in leg and lungs. The reported associations between both COVID-19 susceptibility and severity and other diseases adds to the identification and stratification of individuals at increased risk, adverse outcomes and long-term effects. Public Library of Science 2021-09-03 /pmc/articles/PMC8415605/ /pubmed/34478452 http://dx.doi.org/10.1371/journal.pone.0256988 Text en © 2021 Papadopoulou et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Papadopoulou, Areti
Musa, Hanan
Sivaganesan, Mathura
McCoy, David
Deloukas, Panos
Marouli, Eirini
COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases
title COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases
title_full COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases
title_fullStr COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases
title_full_unstemmed COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases
title_short COVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases
title_sort covid-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415605/
https://www.ncbi.nlm.nih.gov/pubmed/34478452
http://dx.doi.org/10.1371/journal.pone.0256988
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