Occupational and Environmental Medicine · 2004 · 40 citations · 15 references
PharmacyNephrologyToxicologyEnvironmental ToxicologyOccupational ToxicologyRenal PathophysiologyNephrotoxicity MechanismsRenal DiseaseRenal Function TestingRenal Function TestsRenal ToxicityBiological MonitoringGlutathione S-transferase ActivityImpaired Kidney FunctionKidney Function MonitoringMethylmalonic Acid AssessmentRenal Biomarkers Of ToxicityRenal Dysfunction BiomarkersTrichloroethylene Toxicity
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.
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IARC Monographs on the Evaluation of Carcinogenic Risks to Humans
A. J. Zuckerman · Journal of Clinical Pathology · 1995 · 8.8K citations · Full text
Medicine, Oncology, Toxicology +14
Current concepts in proteinuria.
K V Waller, Kory M. Ward, John D. Mahan et al. · Clinical Chemistry · 1989 · 142 citations