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Relationship between shift work and the onset of rheumatoid arthritis

BACKGROUND: Environmental factors play a prominent role in rheumatoid arthritis (RA) aetiology. Shift work has previously been associated with increased RA risk in females. The aim of this study was to investigate the potential association, including a dose–response association, between permanent ni...

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Autores principales: Hedström, Anna Karin, Åkerstedt, Torbjörn, Klareskog, Lars, Alfredsson, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706490/
https://www.ncbi.nlm.nih.gov/pubmed/29225920
http://dx.doi.org/10.1136/rmdopen-2017-000475
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author Hedström, Anna Karin
Åkerstedt, Torbjörn
Klareskog, Lars
Alfredsson, Lars
author_facet Hedström, Anna Karin
Åkerstedt, Torbjörn
Klareskog, Lars
Alfredsson, Lars
author_sort Hedström, Anna Karin
collection PubMed
description BACKGROUND: Environmental factors play a prominent role in rheumatoid arthritis (RA) aetiology. Shift work has previously been associated with increased RA risk in females. The aim of this study was to investigate the potential association, including a dose–response association, between permanent night shift work, rotating shift work and day-oriented shift work and risk of developing anticitrullinated peptide antibodies (ACPA)-positive and ACPA-negative RA. METHODS: The present report is based on a population-based, case–control study with incident cases of RA (1951 cases and 2225 controls matched by age, gender and residential area). Using logistic regression, occurrence of RA among subjects who have been exposed to different kinds of shift work was compared with that among those who have never been exposed by calculating the OR with a 95% CI. RESULTS: Rotating shift work and day-oriented shift work increased the risk of developing ACPA-positive RA (OR 1.3, 95% CI 1.0 to 1.7 and OR 1.3, 95% CI 1.0 to 1.6), but not ACPA-negative RA. Permanent night shift work appeared to be a protective factor both against ACPA-positive RA (OR 0.7, 95% CI 0.6 to 0.9) and ACPA-negative RA (OR 0.8, 95% CI 0.6 to 1.0). For both subsets of RA, significant trends showed a lower risk of developing RA with increasing duration of permanent night shift work (p value for trend 0.002 vs 0.04). CONCLUSIONS: Sleep restriction as a consequence of shift work is associated with several biological effects among which changes in melatonin production may be involved. The present epidemiological findings of a complex relationship between sleep patterns and different forms of RA may be of importance for increasing the understanding of the pathophysiology of RA.
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spelling pubmed-57064902017-12-08 Relationship between shift work and the onset of rheumatoid arthritis Hedström, Anna Karin Åkerstedt, Torbjörn Klareskog, Lars Alfredsson, Lars RMD Open Rheumatoid Arthritis BACKGROUND: Environmental factors play a prominent role in rheumatoid arthritis (RA) aetiology. Shift work has previously been associated with increased RA risk in females. The aim of this study was to investigate the potential association, including a dose–response association, between permanent night shift work, rotating shift work and day-oriented shift work and risk of developing anticitrullinated peptide antibodies (ACPA)-positive and ACPA-negative RA. METHODS: The present report is based on a population-based, case–control study with incident cases of RA (1951 cases and 2225 controls matched by age, gender and residential area). Using logistic regression, occurrence of RA among subjects who have been exposed to different kinds of shift work was compared with that among those who have never been exposed by calculating the OR with a 95% CI. RESULTS: Rotating shift work and day-oriented shift work increased the risk of developing ACPA-positive RA (OR 1.3, 95% CI 1.0 to 1.7 and OR 1.3, 95% CI 1.0 to 1.6), but not ACPA-negative RA. Permanent night shift work appeared to be a protective factor both against ACPA-positive RA (OR 0.7, 95% CI 0.6 to 0.9) and ACPA-negative RA (OR 0.8, 95% CI 0.6 to 1.0). For both subsets of RA, significant trends showed a lower risk of developing RA with increasing duration of permanent night shift work (p value for trend 0.002 vs 0.04). CONCLUSIONS: Sleep restriction as a consequence of shift work is associated with several biological effects among which changes in melatonin production may be involved. The present epidemiological findings of a complex relationship between sleep patterns and different forms of RA may be of importance for increasing the understanding of the pathophysiology of RA. BMJ Publishing Group 2017-08-29 /pmc/articles/PMC5706490/ /pubmed/29225920 http://dx.doi.org/10.1136/rmdopen-2017-000475 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Rheumatoid Arthritis
Hedström, Anna Karin
Åkerstedt, Torbjörn
Klareskog, Lars
Alfredsson, Lars
Relationship between shift work and the onset of rheumatoid arthritis
title Relationship between shift work and the onset of rheumatoid arthritis
title_full Relationship between shift work and the onset of rheumatoid arthritis
title_fullStr Relationship between shift work and the onset of rheumatoid arthritis
title_full_unstemmed Relationship between shift work and the onset of rheumatoid arthritis
title_short Relationship between shift work and the onset of rheumatoid arthritis
title_sort relationship between shift work and the onset of rheumatoid arthritis
topic Rheumatoid Arthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706490/
https://www.ncbi.nlm.nih.gov/pubmed/29225920
http://dx.doi.org/10.1136/rmdopen-2017-000475
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