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Association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from UK Biobank

BACKGROUND: This study aimed to study the association between shift work and incident and fatal cardiovascular disease (CVD), and to explore modifying and mediating factors. METHODS: This is a population-based, prospective cohort study with a median follow-up of 11 years; 238 661 UK Biobank particip...

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Autores principales: Ho, Frederick K, Celis-Morales, Carlos, Gray, Stuart R, Demou, Evangelia, Mackay, Daniel, Welsh, Paul, Katikireddi, S Vittal, Sattar, Naveed, Pell, Jill P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082805/
https://www.ncbi.nlm.nih.gov/pubmed/34414428
http://dx.doi.org/10.1093/ije/dyab144
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author Ho, Frederick K
Celis-Morales, Carlos
Gray, Stuart R
Demou, Evangelia
Mackay, Daniel
Welsh, Paul
Katikireddi, S Vittal
Sattar, Naveed
Pell, Jill P
author_facet Ho, Frederick K
Celis-Morales, Carlos
Gray, Stuart R
Demou, Evangelia
Mackay, Daniel
Welsh, Paul
Katikireddi, S Vittal
Sattar, Naveed
Pell, Jill P
author_sort Ho, Frederick K
collection PubMed
description BACKGROUND: This study aimed to study the association between shift work and incident and fatal cardiovascular disease (CVD), and to explore modifying and mediating factors. METHODS: This is a population-based, prospective cohort study with a median follow-up of 11 years; 238 661 UK Biobank participants who were in paid employment or self-employed at baseline assessment were included. RESULTS: Shift workers had higher risk of incident [hazard ratio (HR) 1.11, 95% confidence interval (CI) 1.06–1.19] and fatal (HR 1.25, 95% CI 1.08–1.44) CVD compared with non-shift workers, after adjusting for socio-economic and work-related factors. The risk was higher with longer duration of shift work, in women and in jobs with little heavy manual labour. Current smoking, short sleep duration, poor sleep quality, adiposity, higher glycated haemoglobin and higher cystatin C were identified as the main potentially modifiable mediators. Mediators collectively explained 52.3% of the associations between shift work and incident CVDs. CONCLUSIONS: Shift workers have higher risk of incident and fatal CVD, partly mediated through modifiable risk factors such as smoking, sleep duration and quality, adiposity and metabolic status. Workplace interventions targeting these mediators have the potential to alleviate shift workers’ CVD risk.
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spelling pubmed-90828052022-05-09 Association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from UK Biobank Ho, Frederick K Celis-Morales, Carlos Gray, Stuart R Demou, Evangelia Mackay, Daniel Welsh, Paul Katikireddi, S Vittal Sattar, Naveed Pell, Jill P Int J Epidemiol Cardiovascular Disease BACKGROUND: This study aimed to study the association between shift work and incident and fatal cardiovascular disease (CVD), and to explore modifying and mediating factors. METHODS: This is a population-based, prospective cohort study with a median follow-up of 11 years; 238 661 UK Biobank participants who were in paid employment or self-employed at baseline assessment were included. RESULTS: Shift workers had higher risk of incident [hazard ratio (HR) 1.11, 95% confidence interval (CI) 1.06–1.19] and fatal (HR 1.25, 95% CI 1.08–1.44) CVD compared with non-shift workers, after adjusting for socio-economic and work-related factors. The risk was higher with longer duration of shift work, in women and in jobs with little heavy manual labour. Current smoking, short sleep duration, poor sleep quality, adiposity, higher glycated haemoglobin and higher cystatin C were identified as the main potentially modifiable mediators. Mediators collectively explained 52.3% of the associations between shift work and incident CVDs. CONCLUSIONS: Shift workers have higher risk of incident and fatal CVD, partly mediated through modifiable risk factors such as smoking, sleep duration and quality, adiposity and metabolic status. Workplace interventions targeting these mediators have the potential to alleviate shift workers’ CVD risk. Oxford University Press 2021-08-20 /pmc/articles/PMC9082805/ /pubmed/34414428 http://dx.doi.org/10.1093/ije/dyab144 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the International Epidemiological Association. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cardiovascular Disease
Ho, Frederick K
Celis-Morales, Carlos
Gray, Stuart R
Demou, Evangelia
Mackay, Daniel
Welsh, Paul
Katikireddi, S Vittal
Sattar, Naveed
Pell, Jill P
Association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from UK Biobank
title Association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from UK Biobank
title_full Association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from UK Biobank
title_fullStr Association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from UK Biobank
title_full_unstemmed Association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from UK Biobank
title_short Association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from UK Biobank
title_sort association and pathways between shift work and cardiovascular disease: a prospective cohort study of 238 661 participants from uk biobank
topic Cardiovascular Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082805/
https://www.ncbi.nlm.nih.gov/pubmed/34414428
http://dx.doi.org/10.1093/ije/dyab144
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