Human Health Effects of Tetrachloroethylene: Key Findings and Scientific Issues

被引:55
作者
Guyton, Kathryn Z. [1 ]
Hogan, Karen A. [1 ]
Scott, Cheryl Siegel [1 ]
Cooper, Glinda S. [1 ]
Bale, Ambuja S. [1 ]
Kopylev, Leonid [1 ]
Barone, Stanley, Jr. [2 ]
Makris, Susan L. [1 ]
Glenn, Barbara [1 ]
Subramaniam, Ravi P. [1 ]
Gwinn, Maureen R. [1 ]
Dzubow, Rebecca C. [3 ]
Chiu, Weihsueh A. [1 ]
机构
[1] US EPA, Natl Ctr Environm Assessment, Washington, DC 20460 USA
[2] US EPA, Off Pollut Prevent & Tox, Washington, DC 20460 USA
[3] US EPA, Off Childrens Hlth Protect, Washington, DC 20460 USA
关键词
LIVER-TUMOR-INDUCTION; PHARMACOKINETIC PBPK MODEL; CANCER-RISK ASSESSMENT; OCCUPATIONAL-EXPOSURE; TRICHLOROACETIC-ACID; DICHLOROACETIC ACID; COLOR-VISION; CHLORINATED SOLVENTS; DRINKING-WATER; PERCHLOROETHYLENE EXPOSURE;
D O I
10.1289/ehp.1307359
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BACKGROUND: The U.S. Environmental Protection Agency (EPA) completed a toxicological review of tetrachloro-ethylene (perchloroethylene, PCE) in February 2012 in support of the Integrated Risk Information System (IRIS). OBJECTIVES: We reviewed key findings and scientific issues regarding the human health effects of PCE described in the U.S. EPA's Toxicological Review of Tetrachloroethylene (Perchloroethylene). METHODS: The updated assessment of PCE synthesized and characterized a substantial database of epidemiological, experimental animal, and mechanistic studies. Key scientific issues were addressed through modeling of PCE toxicokinetics, synthesis of evidence from neurological studies, and analyses of toxicokinetic, mechanistic, and other factors (tumor latency, severity, and background rate) in interpreting experimental animal cancer findings. Considerations in evaluating epidemiological studies included the quality (e.g., specificity) of the exposure assessment methods and other essential design features, and the potential for alternative explanations for observed associations (e.g., bias or confounding). DISCUSSION: Toxicokinetic modeling aided in characterizing the complex metabolism and multiple metabolites that contribute to PCE toxicity. The exposure assessment approach-a key evaluation factor for epidemiological studies of bladder cancer, non-Hodgkin lymphoma, and multiple myeloma-provided suggestive evidence of carcinogenicity. Bioassay data provided conclusive evidence of carcinogenicity in experimental animals. Neurotoxicity was identified as a sensitive non-cancer health effect, occurring at low exposures: a conclusion supported by multiple studies. Evidence was integrated from human, experimental animal, and mechanistic data sets in assessing adverse health effects of PCE. CONCLUSIONS: PCE is likely to be carcinogenic to humans. Neurotoxicity is a sensitive adverse health effect of PCE.
引用
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页码:325 / 334
页数:10
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