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i

Nurses

Supporting Files
File Language:
English


Details

  • Alternative Title:
    Cancer Epidemiol Biomarkers Prev
  • Personal Author:
  • 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.

  • Subjects:
  • Source:
    Cancer Epidemiol Biomarkers Prev. 28(7):1177-1186
  • Pubmed ID:
    31142495
  • Pubmed Central ID:
    PMC6750706
  • Document Type:
  • Funding:
  • Volume:
    28
  • Issue:
    7
  • Collection(s):
  • Main Document Checksum:
    urn:sha256:2296ccb3be3a52b06ce809c84597df39926a614396d208eba6231dbb87de6a14
  • Download URL:
  • File Type:
    Filetype[PDF - 758.93 KB ]
File Language:
English
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