Biological monitoring of kidney function among workers occupationally exposed to trichloroethylene

Occup Environ Med. 2004 Apr;61(4):312-7. doi: 10.1136/oem.2003.007153.

Abstract

Aims: To investigate the nephrotoxic potential of trichloroethylene in a currently exposed population using sensitive urinary markers of kidney toxicity.

Methods: Renal dysfunction was monitored in a cross-sectional study of 70 workers currently exposed to trichloroethylene. An age and sex matched control population of 54 individuals was drawn from hospital and administrative staff.

Results: The mean exposure to trichloroethylene, estimated from urinary trichloroacetic acid concentrations, was 32 ppm (range 0.5-252 ppm) with an average duration of exposure of 4.1 years (range 1-20 years). Significant differences between the exposed and control populations were found for nephrotoxicity markers N-acetylglucosaminidase (NAG) and albumin, and for the mode of action marker, formic acid. However, neither NAG nor albumin showed a significant correlation with either the magnitude or duration of exposure to trichloroethylene. There was a significant correlation between urinary formic acid and trichloroacetic acid concentrations. Within the exposed population there were dose dependent increases in urinary methylmalonic acid concentrations and urinary glutathione S-transferase alpha activity. Although still within the control range, these changes were clearly dose dependent and consistent with one of the proposed mechanisms of trichloroethylene induced kidney toxicity.

Conclusion: Although there was no evidence of kidney toxicity within the population studied, the results suggest that kidney damage could occur at exposure concentrations higher (>250 ppm) than those encountered in this study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / urine
  • Cross-Sectional Studies
  • Environmental Monitoring / methods
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Humans
  • Kidney Diseases / chemically induced*
  • Kidney Diseases / physiopathology
  • Kidney Diseases / urine
  • Male
  • Occupational Exposure / adverse effects*
  • Solvents / toxicity*
  • Time Factors
  • Trichloroethylene / toxicity*

Substances

  • Biomarkers
  • Solvents
  • Trichloroethylene