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  2. Internal Doses of Glycidol in Children and Estimation of Associated Cancer Risk

Internal Doses of Glycidol in Children and Estimation of Associated Cancer Risk

  • Toxics. 2019 Feb 1;7(1):7. doi: 10.3390/toxics7010007.
Jenny Aasa 1 Efstathios Vryonidis 2 Lilianne Abramsson-Zetterberg 3 Margareta Törnqvist 4
Affiliations

Affiliations

  • 1 Department of Environmental Science and Analytical Chemistry, Stockholm University, 106 91 ‎Stockholm, Sweden. [email protected].
  • 2 Department of Environmental Science and Analytical Chemistry, Stockholm University, 106 91 ‎Stockholm, Sweden. [email protected].
  • 3 National Food Agency, 751 26 Uppsala, Sweden. [email protected].
  • 4 Department of Environmental Science and Analytical Chemistry, Stockholm University, 106 91 ‎Stockholm, Sweden. [email protected].
Abstract

The general population is exposed to the genotoxic carcinogen glycidol via food containing refined edible oils where glycidol is present in the form of fatty acid esters. In this study, internal (in vivo) doses of glycidol were determined in a cohort of 50 children and in a reference group of 12 adults (non-smokers and smokers). The lifetime in vivo doses and intakes of glycidol were calculated from the levels of the Hemoglobin (Hb) adduct N-(2,3-dihydroxypropyl)valine in blood samples from the subjects, demonstrating a fivefold variation between the children. The estimated mean intake (1.4 μg/kg/day) was about two times higher, compared to the estimated intake for children by the European Food Safety Authority. The data from adults indicate that the non-smoking and smoking subjects are exposed to about the same or higher levels compared to the children, respectively. The estimated lifetime Cancer risk (200/10⁵) was calculated by a multiplicative risk model from the lifetime in vivo doses of glycidol in the children, and exceeds what is considered to be an acceptable Cancer risk. The results emphasize the importance to further clarify exposure to glycidol and Other possible precursors that could give a contribution to the observed adduct levels.

Keywords

Hb adduct; N-(2.3-dihydroxypropyl)valine; UPLC/MS/MS; cancer risk; glycidol; in vivo.

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