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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.
  • Clift AK; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK ashley.clift@phc.ox.ac.uk.
  • von Ende A; Cancer Research UK Oxford Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Tan PS; Clinical Trial Service Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Sallis HM; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Lindson N; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • Coupland CAC; School of Psychological Science, University of Bristol, Bristol, UK.
  • Munafò MR; NIHR Bristol Biomedical Research Centre, University Hospitals Bristol NHS Foundation Trust and University of Bristol, Bristol, UK.
  • Aveyard P; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Hippisley-Cox J; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Hopewell JC; Division of Primary Care, University of Nottingham, Nottingham, UK.
Thorax ; 77(1): 65-73, 2022 01.
Article in English | MEDLINE | ID: covidwho-1440837
ABSTRACT

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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Limits: Humans Country/Region as subject: Europa Language: English Journal: Thorax Year: 2022 Document Type: Article Affiliation country: Thoraxjnl-2021-217080

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Limits: Humans Country/Region as subject: Europa Language: English Journal: Thorax Year: 2022 Document Type: Article Affiliation country: Thoraxjnl-2021-217080