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Shiftwork, long working hours, and markers of inflammation in a national US population-based sample of employed black and white men and women aged ≥45 years

Supporting Files
File Language:
English


Details

  • Alternative Title:
    Occup Environ Med
  • Personal Author:
  • Description:
    Objectives:

    Work schedule demands contribute to circadian disruption and may influence health via an inflammatory response. We examined the impact of shiftwork and long work hours on inflammation in a national U.S. sample.

    Methods:

    Participants included 12,487 employed Black and White men and women aged ≥45 years enrolled in the REasons for Geographic and Racial Differences in Stroke (REGARDS) Study who completed an occupational questionnaire (2011-2013) and clinical exam (2013-2016). Cross-sectional associations between shiftwork and work hours with log-transformed high-sensitivity C-reactive protein (CRP) and white blood cell count (WBC) were examined by multiple linear regression analysis, overall and by race-sex subgroups.

    Results:

    Overall, rotating shift workers had higher log-CRP concentration compared to day workers (β = 0.09, 95% CI:0.02-0.16) and findings for WBC were null. Black women had the highest geometric mean CRP (2.82 mg/L), while White men had the highest WBC (6.35x109 cells/L). White men who worked afternoons had higher log-CRP compared to those who worked days (β=0.20, 95% CI: 0.08-0.33). Black men engaged in shiftwork <10 years working ≥55 hours/week had higher log-CRP and log-WBC compared to those working days <55 hours/week (β=0.33, 95% CI: 0.02-0.64 and β=0.10, 95% CI: 0.003-0.19). Among shift workers, non-retired White women working forward and backward shift rotations had higher log-CRP compared to those working forward only (β=0.49, 95% CI: 0.02-0.96).

    Conclusions:

    Shift workers had higher inflammatory markers compared to day workers and race-sex disparities should be examined further. These findings highlight a potential biological pathway linking work schedule demands and chronic disease.

  • Subjects:
  • Keywords:
  • Source:
    Occup Environ Med. 80(11):635-643
  • Pubmed ID:
    37813482
  • Pubmed Central ID:
    PMC10936900
  • Document Type:
  • Funding:
  • Volume:
    80
  • Issue:
    11
  • Collection(s):
  • Main Document Checksum:
    urn:sha-512:1c0cd9c8c40cf0a627e019da941fc99a7869f830b24a337646f700617a1f0d9fd00286d4bd814a62619e79459cf7f076f458bba5db52b95de439ddb692eb9bfc
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  • File Type:
    Filetype[PDF - 468.47 KB ]
File Language:
English
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