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A systematical association analysis of 25 common virus infection and genetic susceptibility of COVID-19 infection
OBJECTIVES: Previous studies identified a number of diseases were associated with 2019 coronavirus disease (COVID-19). However, the associations between these diseases related viral infections and COVID-19 remains unknown now. METHODS: In this study, we utilized single nucleotide polymorphisms (SNPs...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Institut Pasteur. Published by Elsevier Masson SAS.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259091/ https://www.ncbi.nlm.nih.gov/pubmed/37315735 http://dx.doi.org/10.1016/j.micinf.2023.105170 |
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author | Zhang, Na Chen, Yujing Li, Chun'e Qin, Xiaoyue He, Dan Wei, Wenming Zhao, Yijing Cai, Qingqing Shi, Sirong Chu, Xiaoge Wen, Yan Jia, Yumeng Zhang, Feng |
author_facet | Zhang, Na Chen, Yujing Li, Chun'e Qin, Xiaoyue He, Dan Wei, Wenming Zhao, Yijing Cai, Qingqing Shi, Sirong Chu, Xiaoge Wen, Yan Jia, Yumeng Zhang, Feng |
author_sort | Zhang, Na |
collection | PubMed |
description | OBJECTIVES: Previous studies identified a number of diseases were associated with 2019 coronavirus disease (COVID-19). However, the associations between these diseases related viral infections and COVID-19 remains unknown now. METHODS: In this study, we utilized single nucleotide polymorphisms (SNPs) related to COVID-19 from genome-wide association study (GWAS) and individual-level genotype data from the UK biobank to calculate polygenic risk scores (PRS) of 487,409 subjects for eight COVID-19 clinical phenotypes. Then, multiple logistic regression models were established to assess the correlation between serological measurements (positive/negative) of 25 viruses and the PRS of eight COVID-19 clinical phenotypes. And we performed stratified analyses by age and gender. RESULTS: In whole population, we identified 12 viruses associated with the PRS of COVID-19 clinical phenotypes, such as VZV seropositivity for Varicella Zoster Virus (Unscreened/Exposed_Negative: β = 0.1361, P = 0.0142; Hospitalized/Unscreened: β = 0.1167, P = 0.0385) and MCV seropositivity for Merkel Cell Polyomavirus (Unscreened/Exposed_Negative: β = −0.0614, P = 0.0478). After age stratification, we identified seven viruses associated with the PRS of eight COVID-19 clinical phenotypes. After gender stratification, we identified five viruses associated with the PRS of eight COVID-19 clinical phenotypes in the women group. CONCLUSION: Our study findings suggest that the genetic susceptibility to different COVID-19 clinical phenotypes is associated with the infection status of various common viruses. |
format | Online Article Text |
id | pubmed-10259091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Institut Pasteur. Published by Elsevier Masson SAS. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102590912023-06-12 A systematical association analysis of 25 common virus infection and genetic susceptibility of COVID-19 infection Zhang, Na Chen, Yujing Li, Chun'e Qin, Xiaoyue He, Dan Wei, Wenming Zhao, Yijing Cai, Qingqing Shi, Sirong Chu, Xiaoge Wen, Yan Jia, Yumeng Zhang, Feng Microbes Infect Original Article OBJECTIVES: Previous studies identified a number of diseases were associated with 2019 coronavirus disease (COVID-19). However, the associations between these diseases related viral infections and COVID-19 remains unknown now. METHODS: In this study, we utilized single nucleotide polymorphisms (SNPs) related to COVID-19 from genome-wide association study (GWAS) and individual-level genotype data from the UK biobank to calculate polygenic risk scores (PRS) of 487,409 subjects for eight COVID-19 clinical phenotypes. Then, multiple logistic regression models were established to assess the correlation between serological measurements (positive/negative) of 25 viruses and the PRS of eight COVID-19 clinical phenotypes. And we performed stratified analyses by age and gender. RESULTS: In whole population, we identified 12 viruses associated with the PRS of COVID-19 clinical phenotypes, such as VZV seropositivity for Varicella Zoster Virus (Unscreened/Exposed_Negative: β = 0.1361, P = 0.0142; Hospitalized/Unscreened: β = 0.1167, P = 0.0385) and MCV seropositivity for Merkel Cell Polyomavirus (Unscreened/Exposed_Negative: β = −0.0614, P = 0.0478). After age stratification, we identified seven viruses associated with the PRS of eight COVID-19 clinical phenotypes. After gender stratification, we identified five viruses associated with the PRS of eight COVID-19 clinical phenotypes in the women group. CONCLUSION: Our study findings suggest that the genetic susceptibility to different COVID-19 clinical phenotypes is associated with the infection status of various common viruses. Institut Pasteur. Published by Elsevier Masson SAS. 2023-06-12 /pmc/articles/PMC10259091/ /pubmed/37315735 http://dx.doi.org/10.1016/j.micinf.2023.105170 Text en © 2023 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Original Article Zhang, Na Chen, Yujing Li, Chun'e Qin, Xiaoyue He, Dan Wei, Wenming Zhao, Yijing Cai, Qingqing Shi, Sirong Chu, Xiaoge Wen, Yan Jia, Yumeng Zhang, Feng A systematical association analysis of 25 common virus infection and genetic susceptibility of COVID-19 infection |
title | A systematical association analysis of 25 common virus infection and genetic susceptibility of COVID-19 infection |
title_full | A systematical association analysis of 25 common virus infection and genetic susceptibility of COVID-19 infection |
title_fullStr | A systematical association analysis of 25 common virus infection and genetic susceptibility of COVID-19 infection |
title_full_unstemmed | A systematical association analysis of 25 common virus infection and genetic susceptibility of COVID-19 infection |
title_short | A systematical association analysis of 25 common virus infection and genetic susceptibility of COVID-19 infection |
title_sort | systematical association analysis of 25 common virus infection and genetic susceptibility of covid-19 infection |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259091/ https://www.ncbi.nlm.nih.gov/pubmed/37315735 http://dx.doi.org/10.1016/j.micinf.2023.105170 |
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