Εndogenous metabolomic responses in circadian disrupted night shift working populations: a scoping review

Behzad Heibati1,2, Paige Lacy2, Konstantinos C Makris1,3

  • 1Precision Exposomics and Health (CLOTHO Lab), Cyprus International Institute for Environmental and Public Health, School of Health Sciences, Cyprus University of Technology, Limassol, Cyprus.

Insights

Night shift work (NSW) disrupts the human metabolome, potentially contributing to early carcinogenicity. This review highlights key metabolic changes and pathways affected by NSW, informing future health strategies for shift workers.

Area of Science:

  • Metabolomics
  • Chronobiology
  • Occupational Health

Background:

  • Night shift work (NSW) is linked to circadian disruption and known carcinogenic potential.
  • Limited research exists on NSW-associated biological pathways and molecules in early carcinogenicity.
  • Metabolomics offers novel exposomics insights into the human endogenous response to NSW.

Purpose of the Study:

  • To conduct a scoping review on how NSW impacts the endogenous human metabolome.
  • To identify key metabolites and biological pathways affected by NSW using metabolomics.
  • To inform strategies for mitigating early-stage carcinogenic effects in shift workers.

Main Methods:

  • Scoping review of human studies on NSW and endogenous biological response.
  • Screening of online databases for original publications.
  • Analysis of 13 included studies (8 occupational, 5 laboratory-based).

Main Results:

  • Consistent reporting of frequently observed metabolites and enriched biological pathways in NSW.
  • Metabolic changes identified in both occupational and simulated NSW settings.
  • Identified pathways provide insights into the early stages of carcinogenicity linked to NSW.

Conclusions:

  • NSW significantly impacts the endogenous human metabolome.
  • Further research is needed to understand complex metabolic changes associated with NSW.
  • Findings can inform strategies to improve shift worker health and mitigate cancer risk.

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