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Nurses
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May 29 2019
Source: Cancer Epidemiol Biomarkers Prev. 28(7):1177-1186
Details:
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Alternative Title:Cancer Epidemiol Biomarkers Prev
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Personal Author:
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Description:Background:
Previous studies associated night-shift work with melatonin disruption, with mixed evidence regarding the modulating effects of chronotype (i.e., diurnal preference).
Methods:
130 active nurses (84 rotating-shift and 46 day-shift workers) in the Nurses’ Health Study II wore a head-mounted light meter and collected spontaneous urine voids over three days. 6-sulfatoxymelatonin (aMT6s), the major urinary metabolite of melatonin, was assessed.
Results:
Rotating-shift workers on night shifts had more light exposure and lower urinary melatonin levels during the night, and urinary melatonin rhythms with smaller peaks (14.83, 95% confidence interval [CI], 11.72–18.75 versus 11.81 ng/mg-creatinine/hour, 95%CI, 9.49–14.71) and later peak onset (4.10, 95%CI, 3.37–4.99 versus 5.71 hours, 95%CI, 4.76–6.85), compared to day-shift workers. Further, evening chronotypes’ melatonin rhythms had later peak onset compared to morning types (4.90 hours, 95%CI, 3.94–6.09 versus 3.64 hours, 95%CI, 2.99–4.43). However, among day-shift workers, morning chronotypes had melatonin rhythms with greater mean levels, larger peaks, and earlier peak onset compared to evening chronotypes; patterns were similar comparing evening versus morning chronotypes among rotating-shift workers on night shifts. The interaction of rotating-shift work and chronotype was significant across all parameters (p<0.05).
Conclusions:
As expected, rotating-shift workers on night shifts had greater light exposure and lower urinary melatonin levels during the night compared to day-shift workers. Intriguingly, melatonin rhythms were dependent on both chronotype and rotating-shift work type, and better alignment of rotating-shift work and chronotype appeared to produce less disrupted melatonin rhythms.
Impact:
The joint effects of shift-work type and chronotype require attention in future studies.
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Subjects:
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Pubmed ID:31142495
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Pubmed Central ID:PMC6750706
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