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The role of vitamin C in pneumonia and COVID-19 infection in adults with European ancestry: a Mendelian randomisation study
BACKGROUND: High dose vitamin C infusion has been proposed to treat critically ill patients, including patients with pneumonia and severe COVID-19. However, trials have shown mixed findings. Here we assessed the unconfounded associations of vitamin C with COVID-19 and pneumonia using the Mendelian r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404179/ https://www.ncbi.nlm.nih.gov/pubmed/34462559 http://dx.doi.org/10.1038/s41430-021-00993-4 |
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author | Hui, L. L. Nelson, E. A. S. Lin, S. L. Zhao, J. V. |
author_facet | Hui, L. L. Nelson, E. A. S. Lin, S. L. Zhao, J. V. |
author_sort | Hui, L. L. |
collection | PubMed |
description | BACKGROUND: High dose vitamin C infusion has been proposed to treat critically ill patients, including patients with pneumonia and severe COVID-19. However, trials have shown mixed findings. Here we assessed the unconfounded associations of vitamin C with COVID-19 and pneumonia using the Mendelian randomisation approach. METHODS: This is a separate-sample Mendelian randomisation study using publicly available data. We applied single nucleotide polymorphisms (SNPs) that were associated with plasma vitamin C, in a recent genome-wide association study (GWAS) as genetic instruments to the GWAS of severe COVID-19, COVID-19 hospitalisation and any infection in the COVID-19 host genetics initiative and the GWAS of pneumonia in the UK Biobank, to assess whether people with genetically predicted higher levels of plasma vitamin C had lower risk of severe COVID-19 and pneumonia. RESULTS: Genetically predicted circulating levels of vitamin C was not associated with susceptibility to severe COVID-19, COVID-19 hospitalisation, any COVID-19 infection nor pneumonia. Similar results were obtained when a weighted median and MR-Egger methods were used. CONCLUSIONS: Mendelian randomisation analysis provided little evidence for an association of genetically predicted circulating levels of vitamin C with COVID-19 or pneumonia and thus our findings provided little support to the use of vitamin C in prevention and treatment in these patients, unless high dose vitamin C infusion has therapeutic effects via different biological pathways. |
format | Online Article Text |
id | pubmed-8404179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84041792021-08-30 The role of vitamin C in pneumonia and COVID-19 infection in adults with European ancestry: a Mendelian randomisation study Hui, L. L. Nelson, E. A. S. Lin, S. L. Zhao, J. V. Eur J Clin Nutr Article BACKGROUND: High dose vitamin C infusion has been proposed to treat critically ill patients, including patients with pneumonia and severe COVID-19. However, trials have shown mixed findings. Here we assessed the unconfounded associations of vitamin C with COVID-19 and pneumonia using the Mendelian randomisation approach. METHODS: This is a separate-sample Mendelian randomisation study using publicly available data. We applied single nucleotide polymorphisms (SNPs) that were associated with plasma vitamin C, in a recent genome-wide association study (GWAS) as genetic instruments to the GWAS of severe COVID-19, COVID-19 hospitalisation and any infection in the COVID-19 host genetics initiative and the GWAS of pneumonia in the UK Biobank, to assess whether people with genetically predicted higher levels of plasma vitamin C had lower risk of severe COVID-19 and pneumonia. RESULTS: Genetically predicted circulating levels of vitamin C was not associated with susceptibility to severe COVID-19, COVID-19 hospitalisation, any COVID-19 infection nor pneumonia. Similar results were obtained when a weighted median and MR-Egger methods were used. CONCLUSIONS: Mendelian randomisation analysis provided little evidence for an association of genetically predicted circulating levels of vitamin C with COVID-19 or pneumonia and thus our findings provided little support to the use of vitamin C in prevention and treatment in these patients, unless high dose vitamin C infusion has therapeutic effects via different biological pathways. Nature Publishing Group UK 2021-08-30 2022 /pmc/articles/PMC8404179/ /pubmed/34462559 http://dx.doi.org/10.1038/s41430-021-00993-4 Text en © The Author(s), under exclusive licence to Springer Nature Limited 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Hui, L. L. Nelson, E. A. S. Lin, S. L. Zhao, J. V. The role of vitamin C in pneumonia and COVID-19 infection in adults with European ancestry: a Mendelian randomisation study |
title | The role of vitamin C in pneumonia and COVID-19 infection in adults with European ancestry: a Mendelian randomisation study |
title_full | The role of vitamin C in pneumonia and COVID-19 infection in adults with European ancestry: a Mendelian randomisation study |
title_fullStr | The role of vitamin C in pneumonia and COVID-19 infection in adults with European ancestry: a Mendelian randomisation study |
title_full_unstemmed | The role of vitamin C in pneumonia and COVID-19 infection in adults with European ancestry: a Mendelian randomisation study |
title_short | The role of vitamin C in pneumonia and COVID-19 infection in adults with European ancestry: a Mendelian randomisation study |
title_sort | role of vitamin c in pneumonia and covid-19 infection in adults with european ancestry: a mendelian randomisation study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404179/ https://www.ncbi.nlm.nih.gov/pubmed/34462559 http://dx.doi.org/10.1038/s41430-021-00993-4 |
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