Background. While perfluorinated compounds (PFCs) are a family of commonly used synthetic compounds with many applications, some PFCs remain persistent within the human body due, in part, to enterohepatic recirculation and renal tubular reabsorption. With increasing recognition of potential harm to human health associated with PFC bioaccumulation, interventions to facilitate elimination of these toxicants are welcome in order to potentially preclude or overcome illness. Minimal research has been undertaken thus far on methods to accelerate human clearance of PFCs. Methods. To test for possible oral treatments to hasten PFC elimination, a group of individuals with elevated PFC levels was treated with cholestyramine (CSM) and, after a break, was subsequently treated with Chlorella pyrenoidosa (CP). Stool samples were collected from all participants (i) prior to any treatment, (ii) during treatment with CSM, and (iii) during treatment with CP. Results. With CSM treatment, significant levels of three distinct PFCs were found in all stools, while levels were mostly undetectable prior to treatment. Following treatment with oral CP, undetectable or very low levels of all PFCs were noted in each sample tested. Conclusion. CSM appears to facilitate elimination of some common PFCs and may have some role in the clinical management of patients with accrued PFCs. 1. Introduction and Background Perfluorinated compounds (PFCs) are a group of anthropogenic chemicals with many useful applications, including repelling stains on furniture/carpets/clothing as well as securing nonadherence in food packaging and nonstick cooking surfaces. Structurally, these compounds consist of a linear or branched carbon backbone, that is, entirely substituted by strong bonds fluorine atoms. The fluorine component of PFCs provides extremely low surface tension and accounts for their unique hydrophobic (water repelling) and lipophobic (lipid repelling) natures [1]. These compounds differ markedly from most other chemical surfactants in that they are very stable, nonreactive, and effective at low concentrations. With these unique properties, selected PFCs have been used to make commercial products that are resistant to both water and oil, are stain resistant, and can also withstand the extremes of temperature, pH, and oxidizing conditions. 1.1. Human PFC Exposure With a number of useful applications, PFC compounds have come into common use in western culture. Human exposure in domestic and commercial settings has occurred as a result of processes such as inhalation of contaminated air,
References
[1]
C. Lau, K. Anitole, C. Hodes, D. Lai, A. Pfahles-Hutchens, and J. Seed, “Perfluoroalkyl acids: a review of monitoring and toxicological findings,” Toxicological Sciences, vol. 99, no. 2, pp. 366–394, 2007.
[2]
“NHANES—Fourth National Report on Exposure to Environmental Chemical Exposures,” 2012, http://www.cdc.gov/exposurereport/pdf/FourthReport.pdf.
[3]
West Virginia University, C. Robert, Byrd Health Sciences Centre, and School of Medicine, Department of Community Medicine, “The C8 health project—WVU data hosting website,” http://www.hsc.wvu.edu/som/cmed/c8/results/otherLaboratoryValues/index.asp.
[4]
D. Chimeddulam and K. Y. Wu, “River water contaminated with perfluorinated compounds potentially posing the greatest risk for young children,” Chemosphere, vol. 90, no. 5, pp. 1617–1624, 2013.
[5]
C. H. Lindh, L. Rylander, G. Toft et al., “Blood serum concentrations of perfluorinated compounds in men from Greenlandic Inuit and European populations,” Chemosphere, vol. 88, no. 11, pp. 1269–1275, 2012.
[6]
H. Fromme, S. A. Tittlemier, W. V?lkel, M. Wilhelm, and D. Twardella, “Perfluorinated compounds—exposure assessment for the general population in Western countries,” International Journal of Hygiene and Environmental Health, vol. 212, no. 3, pp. 239–270, 2009.
[7]
H. Fromme, C. Mosch, M. Morovitz et al., “Pre- and postnatal exposure to perfluorinated compounds (PFCs),” Environmental Science and Technology, vol. 44, no. 18, pp. 7123–7129, 2010.
[8]
C. Thomsen, L. S. Haug, H. Stigum, M. Fr?shaug, S. L. Broadwell, and G. Becher, “Changes in concentrations of perfluorinated compounds, polybrominated diphenyl ethers, and polychlorinated biphenyls in Norwegian breast-milk during twelve months of lactation,” Environmental Science and Technology, vol. 44, no. 24, pp. 9550–9556, 2010.
[9]
K. Harada, K. Inoue, A. Morikawa, T. Yoshinaga, N. Saito, and A. Koizumi, “Renal clearance of perfluorooctane sulfonate and perfluorooctanoate in humans and their species-specific excretion,” Environmental Research, vol. 99, no. 2, pp. 253–261, 2005.
[10]
C. Lau, “Perfluorinated compounds,” Experientia Supplementum, vol. 101, pp. 47–86, 2012.
[11]
G. Olsen, D. Ehresman, J. Froelich, J. Burris, and J. Butenhoff J, “Poster presentation, evaluation of the half-life (T1/2) of elimination of perfluorooctane sulfonate (PFOS), perfluorohexanesulfonate (PFHxS) and perfluorooctanoate (PFOA) from human serum,” 2012, http://www.chem.utoronto.ca/symposium/fluoros/pdfs/TOX017Olsen.pdf.
[12]
OECD, “Hazard assessment of perfluorooctane sulfonate and its salts,” ENV/JM/EXCH, 8, Paris, France, 2002.
[13]
K. W. Whitworth, L. S. Haug, D. D. Baird et al., “Perfluorinated compounds in relation to birth weight in the Norwegian mother and child cohort study,” The American Journal of Epidemiology, vol. 175, no. 12, pp. 1209–1216, 2012.
[14]
K. W. Whitworth, L. S. Haug, D. D. Baird et al., “Perfluorinated compounds and subfecundity in pregnant women,” Epidemiology, vol. 23, no. 2, pp. 257–263, 2012.
[15]
C. Fei, J. K. McLaughlin, R. E. Tarone, and J. Olsen, “Fetal growth indicators and perfluorinated chemicals: a study in the Danish national birth cohort,” The American Journal of Epidemiology, vol. 168, no. 1, pp. 66–72, 2008.
[16]
K. Wu, X. Xu, L. Peng, J. Liu, Y. Guo, and X. Huo, “Association between maternal exposure to perflurooctanic acid (PFOA) from electronic waste recycling and neonatal health outcomes,” Environmental International, vol. 48, pp. 1–8, 2012.
[17]
G. M. Louis, C. M. Peterson, Z. Chen et al., “Perfluorochemicals and endometriosis: the ENDO study,” Epidemiology, vol. 23, no. 6, pp. 799–805, 2012.
[18]
G. Toft, B. A. J?nsson, C. H. Lindh et al., “Exposure to perfluorinated compounds and human semen quality in Arctic and European populations,” Human Reproduction, vol. 27, no. 8, pp. 2532–2540, 2012.
[19]
A. Vested, C. H. Ramlau-Hansen, S. F. Olsen et al., “Associations of in utero exposure to perfluorinated alkyl acids with human semen quality and reproductive hormones in adult men,” Environmental Health Perspectives, vol. 121, no. 4, pp. 453–458, 2013.
[20]
A. Shankar, J. Xiao J, and A. Ducatman, “Perfluooctanoic acid and cardiovascular disease in US adults,” Archives of Internal Medicine, vol. 172, pp. 1397–1403, 2012.
[21]
C. Y. Lin, L. Y. Lin, T. W. Wen et al., “Association between levels of serum perfluorooctane sulfate and carotid artery intima-media thickness in adolescents and young adults,” International Journal of Cardiology, 2013.
[22]
E. P. Hines, S. S. White, J. P. Stanko, E. A. Gibbs-Flournoy, C. Lau, and S. E. Fenton, “Phenotypic dichotomy following developmental exposure to perfluorooctanoic acid (PFOA) in female CD-1 mice: low doses induce elevated serum leptin and insulin, and overweight in mid-life,” Molecular and Cellular Endocrinology, vol. 304, no. 1-2, pp. 97–105, 2009.
[23]
S. A. Uhl, T. James-Todd, and M. L. Bell, “Association of osteoarthritis with perfluorooctanoate and perfluorooctane sulfonate in NHANES, 2003–2008,” Environmental Health Perspectives, vol. 121, no. 4, pp. 447–452, 2013.
[24]
S. Nakayama, K. Harada, K. Inoue et al., “Distributions of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) in Japan and their toxicities,” Environmental Sciences, vol. 12, no. 6, pp. 293–313, 2005.
[25]
C. R. Stein and D. A. Savitz, “Serum perfluorinated compound concentration and attention deficit/hyperactivity disorder in children 5–18 years of age,” Environmental Health Perspectives, vol. 119, no. 10, pp. 1466–1471, 2011.
[26]
K. Hoffman, T. F. Webster, M. G. Weisskopf, J. Weinberg, and V. M. Vieira, “Exposure to polyfuoroalkyl chemicals and attention deficit/hyperactivity disorder in U.S. children 12–15 years of age,” Environmental Health Perspectives, vol. 118, no. 12, pp. 1762–1767, 2010.
[27]
M. C. Power, T. F. Webster, A. A. Baccarelli, and M. G. Weisskopf, “Cross-sectional association between polyfluoroalkyl chemicals and cognitive limitation in the national health and nutrition examination survey,” Neuroepidemiology, vol. 40, no. 2, pp. 125–132, 2013.
[28]
J. C. Dewitt, M. M. Peden-Adams, J. M. Keller, and D. R. Germolec, “Immunotoxicity of perfluorinated compounds: recent developments,” Toxicologic Pathology, vol. 40, no. 2, pp. 300–311, 2012.
[29]
P. Grandjean, E. W. Andersen, E. Budtz-J?rgensen et al., “Serum vaccine antibody concentrations in children exposed to perfluorinated compounds,” The Journal of the American Medical Association, vol. 307, no. 4, pp. 391–397, 2012.
[30]
L. S. Kjeldsen and E. C. Bonefeld-Jorgensen, “Perfluorinated compounds affect the function of sex hormone receptors,” Environmental Science and Pollution Research, 2013.
[31]
S. J. Genuis, M. E. Sears, G. Schwalfenberg, J. Hope, and R. Bernhoft, “Clinical detoxification: elimination of persistent toxicants from the human body,” The Scientific World Journal, vol. 2013, Article ID 238347, 3 pages, 2013.
[32]
S. J. Genuis, S. Beesoon, and D. Birkholz, “Biomonitoring and elimination of perfluorinated compounds (PFCs) and polychlorinated biphenyls (PCBs): blood, urine, and sweat (BUS) study,” ISRN Toxicology. In press.
[33]
F. Scaldaferri, M. Pizzoferrato, F. R. Ponziani, G. Gasbarrini, and A. Gasbarrini, “Use and indications of cholestyramine and bile acid sequestrants,” Internal and Emergency Medicine, vol. 8, no. 3, pp. 205–210, 2013.
[34]
J. D. Johnson, S. J. Gibson, and R. E. Ober, “Cholestyramine-enhanced fecal elimination of carbon-14 in rats after administration of ammonium [14C]perfluorooctanoate or potassium [14C]perfluorooctanesulfonate,” Fundamental and Applied Toxicology, vol. 4, no. 6, pp. 972–976, 1984.
[35]
S. J. Genuis, D. Birkholz, M. Ralitsch, and N. Thibault, “Human detoxification of perfluorinated compounds,” Public Health, vol. 124, no. 7, pp. 367–375, 2010.
[36]
W. J. Cohn, J. J. Boylan, R. V. Blanke, M. W. Fariss, J. R. Howell, and P. S. Guzelian, “Treatment of chlordecone (Kepone) toxicity with cholestyramine. Results of a controlled clinical trial,” The New England Journal of Medicine, vol. 298, no. 5, pp. 243–248, 1978.
[37]
K. L. Underhill, B. A. Rotter, B. K. Thompson, D. B. Prelusky, and H. L. Trenholm, “Effectiveness of cholestyramine in the detoxification of zearalenone as determined in mice,” Bulletin of Environmental Contamination and Toxicology, vol. 54, no. 1, pp. 128–134, 1995.
[38]
G. Avantaggaito, M. Solfrizzo, and A. Visconti, “Recent advances on the use of adsorbent materials for detoxification of Fusarium mycotoxins,” Food Additives and Contaminants, vol. 22, no. 4, pp. 379–388, 2005.
[39]
S. Nakano, H. Takekoshi, and M. Nakano, “Chlorella (Chlorella pyrenoidosa) supplementation decreases dioxin and increases immunoglobulin A concentrations in breast milk,” Journal of Medicinal Food, vol. 10, no. 1, pp. 134–142, 2007.
[40]
R. S. Pore, “Detoxification of chlordecone poisoned rats with chlorella and chlorella derived sporopollenin,” Drug and Chemical Toxicology, vol. 7, no. 1, pp. 57–71, 1984.
[41]
J. Y. Shim, H. S. Shin, J. G. Han et al., “Protective effects of Chlorella vulgaris on liver toxicity in cadmium-administered rats,” Journal of Medicinal Food, vol. 11, no. 3, pp. 479–485, 2008.
[42]
A. Robinson, N. M. Johnson, A. Strey et al., “Calcium montmorillonite clay reduces urinary biomarkers of fumonisin B1 exposure in rats and humans,” Food Additives and Contaminants A, vol. 29, no. 5, pp. 809–818, 2012.
[43]
S. J. Genuis, “Elimination of persistent toxicants from the human body,” Human and Experimental Toxicology, vol. 30, no. 1, pp. 3–18, 2011.
[44]
I. Lee and H. Viberg, “A single neonatal exposure to perfluorohexane sulfonate (PFHxS) affects the levels of important neuroproteins in the developing mouse brain,” Neurotoxicology, vol. 37, pp. 190–196, 2013.
[45]
H. Viberg, I. Lee, and P. Eriksson, “Adult dose-dependent behavarioral and cognitive disturbances after a single neonatal PFHxS dose,” Toxicology, vol. 304, pp. 185–191, 2013.
[46]
L. Cui, C. Y. Liao, Q. F. Zhou, T. M. Xia, Z. J. Yun, and G. B. Jiang, “Excretion of PFOA and PFOS in male rats during a subchronic exposure,” Archives of Environmental Contamination and Toxicology, vol. 58, no. 1, pp. 205–213, 2010.
[47]
S. Beesoon, S. J. Genuis, J .P. Benskin, and J. W. Martin, “Exceptionally high serum concentrations of perfluorohexanesulfonate in a Canadian family are linked to home carpet treatment applications,” Environ Science and Technology, vol. 46, no. 23, pp. 12960–12967, 2012.
[48]
R. J. Jandacek, N. Anderson, M. Liu, S. Zheng, Q. Yang, and P. Tso, “Effects of yo-yo diet, caloric restriction, and olestra on tissue distribution of hexachlorobenzene,” The American Journal of Physiology—Gastrointestinal and Liver Physiology, vol. 288, no. 2, pp. G292–G299, 2005.