Author
Listed:
- Monica Kanki
(Baker Heart and Diabetes Institute
Monash University)
- Artika P. Nath
(Baker Heart and Diabetes Institute)
- Ruidong Xiang
(Baker Heart and Diabetes Institute)
- Stephanie Yiallourou
(Monash University)
- Peter J. Fuller
(Centre of Endocrinology and Metabolism, Hudson Institute of Medical Research)
- Timothy J. Cole
(Monash University)
- Rodrigo Cánovas
(Baker Heart and Diabetes Institute
CSIRO)
- Morag J. Young
(Baker Heart and Diabetes Institute
University of Melbourne)
Abstract
Disrupted circadian rhythms have been linked to an increased risk of hypertension and cardiovascular disease. However, many studies show inconsistent findings and are not sufficiently powered for targeted subgroup analyses. Using the UK Biobank cohort, we evaluate the association between circadian rhythm-disrupting behaviours, blood pressure (SBP, DBP) and inflammatory markers in >350,000 adults with European white British ancestry. The independent U-shaped relationship between sleep length and SBP/DBP is most prominent with a low inflammatory status. Poor sleep quality and permanent night shift work are also positively associated with SBP/DBP. Although fully adjusting for BMI in the linear regression model attenuated effect sizes, these associations remain significant. Two-sample Mendelian Randomisation (MR) analyses support a potential causal effect of long sleep, short sleep, chronotype, daytime napping and sleep duration on SBP/DBP. Thus, in the current study, we present a positive association between circadian rhythm-disrupting behaviours and SBP/DBP regulation in males and females that is largely independent of age.
Suggested Citation
Monica Kanki & Artika P. Nath & Ruidong Xiang & Stephanie Yiallourou & Peter J. Fuller & Timothy J. Cole & Rodrigo Cánovas & Morag J. Young, 2023.
"Poor sleep and shift work associate with increased blood pressure and inflammation in UK Biobank participants,"
Nature Communications, Nature, vol. 14(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42758-6
DOI: 10.1038/s41467-023-42758-6
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