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Extensive Mendelian randomization study identifies potential causal risk factors for severe COVID-19

BACKGROUND: Identifying causal risk factors for severe coronavirus disease 2019 (COVID-19) is critical for its prevention and treatment. Many associated pre-existing conditions and biomarkers have been reported, but these observational associations suffer from confounding and reverse causation. METH...

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Autores principales: Sun, Yitang, Zhou, Jingqi, Ye, Kaixiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053245/
https://www.ncbi.nlm.nih.gov/pubmed/35602208
http://dx.doi.org/10.1038/s43856-021-00061-9
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author Sun, Yitang
Zhou, Jingqi
Ye, Kaixiong
author_facet Sun, Yitang
Zhou, Jingqi
Ye, Kaixiong
author_sort Sun, Yitang
collection PubMed
description BACKGROUND: Identifying causal risk factors for severe coronavirus disease 2019 (COVID-19) is critical for its prevention and treatment. Many associated pre-existing conditions and biomarkers have been reported, but these observational associations suffer from confounding and reverse causation. METHODS: Here, we perform a large-scale two-sample Mendelian randomization (MR) analysis to evaluate the causal roles of many traits in severe COVID-19. RESULTS: Our results highlight multiple body mass index (BMI)-related traits as risk-increasing: BMI (OR: 1.89, 95% CI: 1.51–2.37), hip circumference (OR: 1.46, 1.15–1.85), and waist circumference (OR: 1.82, 1.36–2.43). Our multivariable MR analysis further suggests that the BMI-related effect might be driven by fat mass (OR: 1.63, 1.03–2.58), but not fat-free mass (OR: 1.00, 0.61–1.66). Several white blood cell counts are negatively associated with severe COVID-19, including those of neutrophils (OR: 0.76, 0.61–0.94), granulocytes (OR: 0.75, 0.601–0.93), and myeloid white blood cells (OR: 0.77, 0.62–0.96). Furthermore, some circulating proteins are associated with an increased risk of (e.g., zinc-alpha-2-glycoprotein) or protection from severe COVID-19 (e.g., prostate-associated microseminoprotein). CONCLUSIONS: Our study suggests that fat mass and white blood cells might be involved in the development of severe COVID-19. It also prioritizes potential risk and protective factors that might serve as drug targets and guide the effective protection of high-risk individuals.
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spelling pubmed-90532452022-05-20 Extensive Mendelian randomization study identifies potential causal risk factors for severe COVID-19 Sun, Yitang Zhou, Jingqi Ye, Kaixiong Commun Med (Lond) Article BACKGROUND: Identifying causal risk factors for severe coronavirus disease 2019 (COVID-19) is critical for its prevention and treatment. Many associated pre-existing conditions and biomarkers have been reported, but these observational associations suffer from confounding and reverse causation. METHODS: Here, we perform a large-scale two-sample Mendelian randomization (MR) analysis to evaluate the causal roles of many traits in severe COVID-19. RESULTS: Our results highlight multiple body mass index (BMI)-related traits as risk-increasing: BMI (OR: 1.89, 95% CI: 1.51–2.37), hip circumference (OR: 1.46, 1.15–1.85), and waist circumference (OR: 1.82, 1.36–2.43). Our multivariable MR analysis further suggests that the BMI-related effect might be driven by fat mass (OR: 1.63, 1.03–2.58), but not fat-free mass (OR: 1.00, 0.61–1.66). Several white blood cell counts are negatively associated with severe COVID-19, including those of neutrophils (OR: 0.76, 0.61–0.94), granulocytes (OR: 0.75, 0.601–0.93), and myeloid white blood cells (OR: 0.77, 0.62–0.96). Furthermore, some circulating proteins are associated with an increased risk of (e.g., zinc-alpha-2-glycoprotein) or protection from severe COVID-19 (e.g., prostate-associated microseminoprotein). CONCLUSIONS: Our study suggests that fat mass and white blood cells might be involved in the development of severe COVID-19. It also prioritizes potential risk and protective factors that might serve as drug targets and guide the effective protection of high-risk individuals. Nature Publishing Group UK 2021-12-09 /pmc/articles/PMC9053245/ /pubmed/35602208 http://dx.doi.org/10.1038/s43856-021-00061-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sun, Yitang
Zhou, Jingqi
Ye, Kaixiong
Extensive Mendelian randomization study identifies potential causal risk factors for severe COVID-19
title Extensive Mendelian randomization study identifies potential causal risk factors for severe COVID-19
title_full Extensive Mendelian randomization study identifies potential causal risk factors for severe COVID-19
title_fullStr Extensive Mendelian randomization study identifies potential causal risk factors for severe COVID-19
title_full_unstemmed Extensive Mendelian randomization study identifies potential causal risk factors for severe COVID-19
title_short Extensive Mendelian randomization study identifies potential causal risk factors for severe COVID-19
title_sort extensive mendelian randomization study identifies potential causal risk factors for severe covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053245/
https://www.ncbi.nlm.nih.gov/pubmed/35602208
http://dx.doi.org/10.1038/s43856-021-00061-9
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