Modeled Perfluorooctanoic Acid (PFOA) Exposure and Liver Function in a Mid-Ohio Valley Community

被引:93
作者
Darrow, Lyndsey A. [1 ,2 ,3 ]
Groth, Alyx C. [2 ]
Winquist, Andrea [2 ,3 ]
Shin, Hyeong-Moo [4 ,5 ]
Bartell, Scott M. [6 ,7 ]
Steenland, Kyle [2 ,3 ]
机构
[1] Univ Nevada, Sch Community Hlth Sci, Reno, NV 89557 USA
[2] Emory Univ, Dept Epidemiol, Atlanta, GA 30322 USA
[3] Emory Univ, Dept Environm Hlth, Atlanta, GA 30322 USA
[4] Univ Calif Davis, Dept Publ Hlth Sci, Davis, CA 95616 USA
[5] Univ Calif Irvine, Sch Social Ecol, Irvine, CA USA
[6] Univ Calif Irvine, Dept Stat, Irvine, CA USA
[7] Univ Calif Irvine, Dept Epidemiol, Irvine, CA USA
关键词
FLUOROCHEMICAL PRODUCTION WORKERS; CATALYTIC ACTIVITY CONCENTRATIONS; AMMONIUM PERFLUOROOCTANOATE; PERFLUOROALKYL ACIDS; SERUM CONCENTRATIONS; US POPULATION; ENZYMES; HEALTH; PLANT; PART;
D O I
10.1289/ehp.1510391
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BACKGROUND: Perfluorooctanoic acid (PFOA or C8) has hepatotoxic effects in animals. Cross-sectional epidemiologic studies suggest PFOA is associated with liver injury biomarkers. OBJECTIVES: We estimated associations between modeled historical PFOA exposures and liver injury biomarkers and medically validated liver disease. METHODS: Participants completed surveys during 2008-2011 reporting demographic, medical, and residential history information. Self-reported liver disease, including hepatitis, fatty liver, enlarged liver and cirrhosis, was validated with healthcare providers. Alanine aminotransferase (ALT), gamma-glutamyltransferase (GGT) and direct bilirubin, markers of liver toxicity, were obtained from blood samples collected in the C8 Health Project (2005-2006). Historically modeled PFOA exposure, estimated using environmental fate and transport models and participant residential histories, was analyzed in relation to liver biomarkers (n = 30,723, including 1,892 workers) and liver disease (n = 32,254, including 3,713 workers). RESULTS: Modeled cumulative serum PFOA was positively associated with ALT levels (p for trend < 0.0001), indicating possible liver toxicity. An increase from the first to the fifth quintile of cumulative PFOA exposure was associated with a 6% increase in ALT levels (95% CI: 4, 8%) and a 16% increased odds of having above-normal ALT (95% CI: odds ratio: 1.02, 1.33%). There was no indication of association with either elevated direct bilirubin or GGT; however, PFOA was associated with decreased direct bilirubin. We observed no evidence of an effect of cumulative exposure (with or without a 10-year lag) on all liver disease (n = 647 cases), nor on enlarged liver, fatty liver, and cirrhosis only (n = 427 cases). CONCLUSION: Results are consistent with previous cross-sectional studies showing association between PFOA and ALT, a marker of hepatocellular damage. We did not observe evidence that PFOA increases the risk of clinically diagnosed liver disease.
引用
收藏
页码:1227 / 1233
页数:7
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