Impact of extended working periods on genomic and telomeric DNA and on inflammatory markers: Results of an intervention study with office workers and carpenters

Mutat Res Genet Toxicol Environ Mutagen. 2018 Dec;836(Pt A):78-81. doi: 10.1016/j.mrgentox.2018.05.004. Epub 2018 May 5.

Abstract

Aim of this study was to clarify if extension of the work phase has an impact on DNA- stability, telomere lengths and inflammatory markers. We conducted an intervention trial with office workers (n = 24) and carpenters (n = 10), who changed their working schedule from 8 to 12 h per day over a period of 3 months. The work of both groups involved only moderate physical activity. We found no evidence for induction of double strand breaks (measured in γH2AX assays) and relative telomere lengths (relTL_36B4 and ALB) in lymphocytes in the two study groups. Furthermore, no overall changes of the levels of C-reactive protein (CRP), interleukin-6 (IL-6) and thiobarbituric acid reactive substances (TBARS) in plasma were detected. However, we found in agreement with earlier investigations a moderate (not significant) increase of the CRP levels with age. Furthermore, significant higher CRP concentrations (P = 0.03) were detected in young individuals (21-30 years) as a consequence of the extended working period. Taken together our findings indicate that prolongation of the working hours has no pronounced impact on DNA stability, telomere shortening and inflammatory markers; but the increase of the CRP concentrations in young workers may be indicative for adverse health effects in this subgroup.

Keywords: DNA instability; Extension of working hours; Inflammatory parameters; Light physical activity; Telomere lengths.

MeSH terms

  • Adult
  • C-Reactive Protein / analysis
  • DNA / analysis*
  • DNA / genetics
  • Employment*
  • Female
  • Humans
  • Inflammation Mediators / blood*
  • Interleukin-6 / blood
  • Male
  • Oxidative Stress
  • Telomere / genetics*
  • Thiobarbituric Acid Reactive Substances
  • Workplace*
  • Young Adult

Substances

  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-6
  • Thiobarbituric Acid Reactive Substances
  • C-Reactive Protein
  • DNA