4.8 Article

Persistent Organic Pollutants and Transthyretin-Bound Thyroxin in Plasma of Inuit Women of Childbearing Age

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 47, Issue 22, Pages 13086-13092

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/es4027634

Keywords

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Funding

  1. Aboriginal Affairs and Northern Development Canada (Northern Contaminants Program)
  2. FRQS Environmental Health Research Network
  3. Quebec Health and Social Services Ministry
  4. Nunavik Regional Board of Health and Social Services
  5. Network of Centers of Excellence of Canada (ArcticNet)
  6. Canadian Foundation for Innovation
  7. FRQS

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The Inuit population of Nunavik (Northern Quebec, Canada) is highly exposed to persistent organic pollutants (POPs) through their traditional diet. Some POPs, i.e., hydroxylated metabolites of polychlorinated biphenyls (OH-PCBs), pentachlorophenol (PCP), and perfluorooctane sulfonate (PFOS), compete with thyroxin (T4) for binding sites on transthyretin (TTR), a T4 transport protein found in plasma and cerebrospinal fluid. We tested the hypothesis that these TTR-binding compounds decrease circulating concentrations of T4 bound to TTR (T4-TTR) in Inuit women of reproductive age. We measured the concentration of T4-TTR in plasma samples obtained from 120 Inuit women (18-39 years old) by combining native-polyacrylamide gel electrophoresis and liquid chromatography-tandem mass spectrometry (LC-MS/MS) techniques. Total T4, TTR, and thyroxin-binding globulin (TBG) concentrations were also determined, while POPs levels had been previously measured. The mean T4-TTR concentration was 8.4 nmol/L (SD = 2.4) with values ranging from 2.9 to 14.4 nmol/L. Linear regression analysis revealed that TTR, TBG, and total T4 concentrations were significant predictors (p < 0.002) of T4-TTR levels (total adjusted R-squared = 0.26, p < 0.0001) but not levels of OH-PCBs, chlorophenols, or PFOS. Our results suggest that circulating levels of these TTR-binding compounds in Inuit women of childbearing age are not high enough to affect TTR-mediated thyroid hormone transport. The possibility of increased delivery of these compounds to the developing brain requires further investigation.

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