Longitudinal follow-up of health effects among workers handling engineered nanomaterials: a panel study

Environ Health. 2019 Dec 9;18(1):107. doi: 10.1186/s12940-019-0542-y.

Abstract

Background: Although no human illness to date is confirmed to be attributed to engineered nanoparticles, occupational epidemiological studies are needed to verify the health effects of nanoparticles. This study used a repeated measures design to explore the potential adverse health effects of workers handling nanomaterials.

Methods: Study population was 206 nanomaterial-handling workers and 108 unexposed controls, who were recruited from 14 nanotechnology plants. They were followed up no less than two times in four years. A questionnaire was used to collect potential confounders and detailed work conditions. Control banding was adopted to categorize risk level for each participant as a surrogate marker of exposure. Health hazard markers include cardiopulmonary dysfunction markers, inflammation and oxidative damage markers, antioxidant enzymes activity, and genotoxicity markers. The Generalized Estimating Equation model was applied to analyze repeated measurements.

Results: In comparison to the controls, a significant dose-dependent increase on risk levels for the change of superoxide dismutase (p<0.01) and a significant increase of glutathione peroxidase change in risk level 1 was found for nanomaterial-handling workers. However, the change of cardiovascular dysfunction, lung damages, inflammation, oxidative damages, neurobehavioral and genotoxic markers were not found to be significantly associated with nanomaterials handling in this panel study.

Conclusions: This repeated measurement study suggests that there was no evidence of potential adverse health effects under the existing workplace exposure levels among nanomaterials handling workers, except for the increase of antioxidant enzymes.

Keywords: Nanomaterials; control banding; follow-up study; health effect markers; panel study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antioxidants / metabolism
  • Biomarkers / analysis*
  • DNA Damage / drug effects
  • Dose-Response Relationship, Drug
  • Female
  • Follow-Up Studies
  • Humans
  • Inflammation / chemically induced
  • Inflammation / epidemiology
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Nanostructures / adverse effects*
  • Nanotechnology*
  • Occupational Exposure / adverse effects*
  • Oxidative Stress / drug effects
  • Taiwan / epidemiology

Substances

  • Antioxidants
  • Biomarkers