The Associations of Chronotype and Shift Work With Rheumatoid Arthritis.
The Associations of Chronotype and Shift Work With Rheumatoid Arthritis.
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DOI:
10.1177/07487304231179595
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发表时间:
2023-10
影响因子:
3.5
通讯作者:
Gibbs, Julie E.
中科院分区:
文献类型:
--
作者:
Butler, Thomas D.;Maidstone, Robert J.;Rutter, Martin K.;McLaughlin, John T.;Ray, David W.;Gibbs, Julie E.
The circadian clock regulates multiple aspects of human physiology including immunity. People have a circadian preference termed chronotype. Those with an evening preference may be better suited to shift work, but also carry higher risk of adverse health. Shift work leads to misalignment of circadian rhythms and is associated with increased risk of inflammatory disease such as asthma and cancer. Here, we investigate the association between chronotype, shift work, and rheumatoid arthritis (RA). The associations between exposures of shift work and chronotype on risk of RA were studied in up to 444,210 U.K. Biobank participants. Multivariable logistic regression models were adjusted for covariates: age, sex, ethnicity, alcohol intake, smoking history, Townsend Deprivation Index (TDI), sleep duration, length of working week, and body mass index (BMI). After adjusting for covariates, individuals with a morning chronotype had lower odds of having rheumatoid arthritis (RA; odds ratio [OR]: 0.93, 95% confidence interval [CI]: 0.88-0.99) when compared to intermediate chronotypes. The association between morning chronotype and RA persisted with a more stringent RA case definition (covariate-adjusted OR: 0.89, 95% CI: 0.81-0.97). When adjusted for age, sex, ethnicity, and TDI, shift workers had higher odds of RA (OR: 1.22, 95% CI: 1.1-1.36) compared to day workers that attenuated to the null after further covariate adjustment (OR: 1.1, 95% CI: 0.98-1.22). Morning chronotypes working permanent night shifts had significantly higher odds of RA compared to day workers (OR: 1.89, 95% CI: 1.19-2.99). These data point to a role for circadian rhythms in RA pathogenesis. Further studies are required to determine the mechanisms underlying this association and understand the potential impact of shift work on chronic inflammatory disease and its mediating factors.
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影响因子:
4.9
作者:
Gibbs JE;Ray DW
通讯作者:
Ray DW
影响因子:
5
作者:
Fry A;Littlejohns TJ;Sudlow C;Doherty N;Adamska L;Sprosen T;Collins R;Allen NE
通讯作者:
Allen NE
影响因子:
10
作者:
Maidstone R;Anderson SG;Ray DW;Rutter MK;Durrington HJ;Blaikley JF
通讯作者:
Blaikley JF
影响因子:
3.5
作者:
Butler, Thomas D.;Ali, Aala Mohammed;Gibbs, Julie E.;McLaughlin, John T.
通讯作者:
McLaughlin, John T.
影响因子:
50
作者:
Foster, Hatnish M. E.;Celis-Morales, Carlos A.;Mair, Frances S.
通讯作者:
Mair, Frances S.