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Published on: August 8, 2019
Endothelial Dysfunction and Hemostatic System Activation in Relation to Shift Workers, Social Jetlag, and Chronotype
Gleb Saharov1,2, Barbara Salti1, Maram Bareya1
1Thrombosis and Hemostasis Unit, Rambam Health Care Campus, Haifa 3109601, Israel.
Insights
Shift work, social jetlag, and late chronotypes impair endothelial function and increase morning thrombotic risk in nurses. Maintaining biological daily rhythms is crucial for cardiovascular health.
Area of Science:
- Cardiovascular Science
- Chronobiology
- Endocrinology
Background:
- Circadian misalignment from shiftwork, social jetlag (SJL), or chronotype may increase cardiovascular disease risk.
- Endothelial dysfunction and hypercoagulability are key predictors of cardiovascular pathology.
Purpose of the Study:
- To investigate the impact of shift work, SJL, and chronotype on endothelial function and coagulation parameters in female nurses.
- To assess diurnal variations in these markers.
Main Methods:
- 100 female nurses underwent endothelial function testing (EndoPAT) and blood sampling for coagulation markers.
- Measurements were taken twice daily (morning and evening).
- Shift workers, day workers, SJL, and chronotype were analyzed.
Main Results:
- Shift workers exhibited lower endothelial function and fibrinogen, with higher plasminogen activator inhibitor-1 (PAI-1) and heparanase levels compared to day workers.
- High SJL correlated with poorer endothelial function and elevated PAI-1, heparanase, and D-Dimer.
- Late chronotypes showed higher PAI-1 and heparanase activity than early chronotypes.
- Diurnal variations were observed for PAI-1, von-Willebrand factor (vWF), heparanase, and heparan-sulfate, with morning peaks.
Conclusions:
- Shift work, high SJL, and late chronotype are associated with endothelial impairment and increased thrombotic risk.
- Thrombotic risk is elevated in the morning, irrespective of the cause of circadian misalignment.
- Adherence to biological daily rhythms is vital; heparanase inhibitors may mitigate risk in misaligned individuals.
Abstract:
Circadian misalignment, due to shiftwork and/or individual chronotype and/or social jetlag (SJL), quantified as the difference between internal and social timing, may contribute to cardiovascular disease. Markers of endothelial dysfunction and activation of the coagulation system may predict cardiovascular pathology. The present study aim was to investigate the effects of shift work, SJL, and chronotype on endothelial function and coagulation parameters. One hundred female nurses underwent endothelial function testing using the EndoPAT and blood sampling for coagulation markers, repeated at 06:00-9:00 and 18:00-21:00. We found that compared with day workers, endothelial function and fibrinogen levels were lower (p = 0.001, p = 0.005, respectively) and the procoagulant parameters of plasminogen activator inhibitor-1 (PAI-1) and heparanase level and activity were higher amongst shift workers (p = 0.009, p = 0.03, p = 0.029, respectively). High SJL was associated with lower endothelial function (p = 0.002) and higher PAI-1, heparanase procoagulant activity, heparanase level, and D-Dimer level (p = 0.004, p = 0.003, p = 0.021, p = 0.006, respectively). In the late chronotype, PAI-1 and heparanase procoagulant activity were higher than in the early chronotype (p = 0.009, p = 0.007, respectively). Diurnal variation was found for PAI-1, von-Willebrand factor (vWF), heparanase, and heparan-sulfate with higher levels in the mornings. The correlation between shift/day workers and SJL or chronotype was moderately strong, indicating that SJL and chronotype are independent factors. In conclusion, findings suggest endothelial impairment and increased thrombotic risk in nurses working in shifts or with high SJL or late chronotype. The thrombotic risk is increased in the morning independent of circadian misalignment cause. These findings strengthen the importance of the alliance to the biological daily rhythm in daily life. Further research is needed to evaluate inhibitors of heparanase to attenuate the thrombotic risk in individuals with circadian misalignment.
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