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Smoking and COVID-19 outcomes: an observational and Mendelian randomisation study using the UK Biobank cohort
BACKGROUND: Conflicting evidence has emerged regarding the relevance of smoking on risk of COVID-19 and its severity. METHODS: We undertook large-scale observational and Mendelian randomisation (MR) analyses using UK Biobank. Most recent smoking status was determined from primary care records (70.8%...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483921/ https://www.ncbi.nlm.nih.gov/pubmed/34580193 http://dx.doi.org/10.1136/thoraxjnl-2021-217080 |
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author | Clift, Ashley K von Ende, Adam Tan, Pui San Sallis, Hannah M Lindson, Nicola Coupland, Carol A C Munafò, Marcus R Aveyard, Paul Hippisley-Cox, Julia Hopewell, Jemma C |
author_facet | Clift, Ashley K von Ende, Adam Tan, Pui San Sallis, Hannah M Lindson, Nicola Coupland, Carol A C Munafò, Marcus R Aveyard, Paul Hippisley-Cox, Julia Hopewell, Jemma C |
author_sort | Clift, Ashley K |
collection | PubMed |
description | BACKGROUND: Conflicting evidence has emerged regarding the relevance of smoking on risk of COVID-19 and its severity. METHODS: We undertook large-scale observational and Mendelian randomisation (MR) analyses using UK Biobank. Most recent smoking status was determined from primary care records (70.8%) and UK Biobank questionnaire data (29.2%). COVID-19 outcomes were derived from Public Health England SARS-CoV-2 testing data, hospital admissions data, and death certificates (until 18 August 2020). Logistic regression was used to estimate associations between smoking status and confirmed SARS-CoV-2 infection, COVID-19-related hospitalisation, and COVID-19-related death. Inverse variance-weighted MR analyses using established genetic instruments for smoking initiation and smoking heaviness were undertaken (reported per SD increase). RESULTS: There were 421 469 eligible participants, 1649 confirmed infections, 968 COVID-19-related hospitalisations and 444 COVID-19-related deaths. Compared with never-smokers, current smokers had higher risks of hospitalisation (OR 1.80, 95% CI 1.26 to 2.29) and mortality (smoking 1–9/day: OR 2.14, 95% CI 0.87 to 5.24; 10–19/day: OR 5.91, 95% CI 3.66 to 9.54; 20+/day: OR 6.11, 95% CI 3.59 to 10.42). In MR analyses of 281 105 White British participants, genetically predicted propensity to initiate smoking was associated with higher risks of infection (OR 1.45, 95% CI 1.10 to 1.91) and hospitalisation (OR 1.60, 95% CI 1.13 to 2.27). Genetically predicted higher number of cigarettes smoked per day was associated with higher risks of all outcomes (infection OR 2.51, 95% CI 1.20 to 5.24; hospitalisation OR 5.08, 95% CI 2.04 to 12.66; and death OR 10.02, 95% CI 2.53 to 39.72). INTERPRETATION: Congruent results from two analytical approaches support a causal effect of smoking on risk of severe COVID-19. |
format | Online Article Text |
id | pubmed-8483921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-84839212021-10-01 Smoking and COVID-19 outcomes: an observational and Mendelian randomisation study using the UK Biobank cohort Clift, Ashley K von Ende, Adam Tan, Pui San Sallis, Hannah M Lindson, Nicola Coupland, Carol A C Munafò, Marcus R Aveyard, Paul Hippisley-Cox, Julia Hopewell, Jemma C Thorax Smoking BACKGROUND: Conflicting evidence has emerged regarding the relevance of smoking on risk of COVID-19 and its severity. METHODS: We undertook large-scale observational and Mendelian randomisation (MR) analyses using UK Biobank. Most recent smoking status was determined from primary care records (70.8%) and UK Biobank questionnaire data (29.2%). COVID-19 outcomes were derived from Public Health England SARS-CoV-2 testing data, hospital admissions data, and death certificates (until 18 August 2020). Logistic regression was used to estimate associations between smoking status and confirmed SARS-CoV-2 infection, COVID-19-related hospitalisation, and COVID-19-related death. Inverse variance-weighted MR analyses using established genetic instruments for smoking initiation and smoking heaviness were undertaken (reported per SD increase). RESULTS: There were 421 469 eligible participants, 1649 confirmed infections, 968 COVID-19-related hospitalisations and 444 COVID-19-related deaths. Compared with never-smokers, current smokers had higher risks of hospitalisation (OR 1.80, 95% CI 1.26 to 2.29) and mortality (smoking 1–9/day: OR 2.14, 95% CI 0.87 to 5.24; 10–19/day: OR 5.91, 95% CI 3.66 to 9.54; 20+/day: OR 6.11, 95% CI 3.59 to 10.42). In MR analyses of 281 105 White British participants, genetically predicted propensity to initiate smoking was associated with higher risks of infection (OR 1.45, 95% CI 1.10 to 1.91) and hospitalisation (OR 1.60, 95% CI 1.13 to 2.27). Genetically predicted higher number of cigarettes smoked per day was associated with higher risks of all outcomes (infection OR 2.51, 95% CI 1.20 to 5.24; hospitalisation OR 5.08, 95% CI 2.04 to 12.66; and death OR 10.02, 95% CI 2.53 to 39.72). INTERPRETATION: Congruent results from two analytical approaches support a causal effect of smoking on risk of severe COVID-19. BMJ Publishing Group 2022-01 2021-09-27 /pmc/articles/PMC8483921/ /pubmed/34580193 http://dx.doi.org/10.1136/thoraxjnl-2021-217080 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Smoking Clift, Ashley K von Ende, Adam Tan, Pui San Sallis, Hannah M Lindson, Nicola Coupland, Carol A C Munafò, Marcus R Aveyard, Paul Hippisley-Cox, Julia Hopewell, Jemma C Smoking and COVID-19 outcomes: an observational and Mendelian randomisation study using the UK Biobank cohort |
title | Smoking and COVID-19 outcomes: an observational and Mendelian randomisation study using the UK Biobank cohort |
title_full | Smoking and COVID-19 outcomes: an observational and Mendelian randomisation study using the UK Biobank cohort |
title_fullStr | Smoking and COVID-19 outcomes: an observational and Mendelian randomisation study using the UK Biobank cohort |
title_full_unstemmed | Smoking and COVID-19 outcomes: an observational and Mendelian randomisation study using the UK Biobank cohort |
title_short | Smoking and COVID-19 outcomes: an observational and Mendelian randomisation study using the UK Biobank cohort |
title_sort | smoking and covid-19 outcomes: an observational and mendelian randomisation study using the uk biobank cohort |
topic | Smoking |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483921/ https://www.ncbi.nlm.nih.gov/pubmed/34580193 http://dx.doi.org/10.1136/thoraxjnl-2021-217080 |
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