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Статья

Comparison of Estimated Dietary Intake of Acrylamide with Hemoglobin Adducts of Acrylamide and Glycidamide

Thomas BjellaasDivision of Environmental Medicine, Norwegian Institute of Public Health, Nydalen, NO-0403 Oslo, NorwayPelle Thonning Olesen‡National Food Institute, Technical University of Denmark, Mørkhøj Bygade 19, DK-2860 Søborg, DenmarkHenrik Lauritz Frandsen‡National Food Institute, Technical University of Denmark, Mørkhøj Bygade 19, DK-2860 Søborg, DenmarkMargaretha Haugen*Division of Environmental Medicine, Norwegian Institute of Public Health, Nydalen, NO-0403 Oslo, NorwayLinn Helene StølenDivision of Environmental Medicine, Norwegian Institute of Public Health, Nydalen, NO-0403 Oslo, NorwayJan Erik Paulsen*Division of Environmental Medicine, Norwegian Institute of Public Health, Nydalen, NO-0403 Oslo, NorwayJan Alexander*Division of Environmental Medicine, Norwegian Institute of Public Health, Nydalen, NO-0403 Oslo, NorwayElsa Lundanes†Department of Chemistry, University of Oslo, PO Box 1033, Blindern, N-0315, NorwayGeorg BecherDivision of Environmental Medicine, Norwegian Institute of Public Health, Nydalen, NO-0403 Oslo, Norway
2007en
ABI

Аннотация

In a study comprising 50 subjects, we investigated the relationship between acrylamide (AA) intake from food using food frequency questionnaires and the concentration of hemoglobin (Hb) adducts of AA and its genotoxic metabolite glycidamide (GA) as a measure of the internal exposure. A method using solid-phase extraction and liquid chromatography with negative electrospray tandem mass spectrometric (MS/MS) detection for the determination of the Hb adducts as phenylthiohydantoin derivatives in human blood was developed. The limit of quantification for AA- and GA-Hb adducts were 2 and 6 pmol/g globin, respectively, and the between-assay precision was below 25%. The estimated dietary intake of AA was (median and range) 13.5 microg/day (4.1-72.6) in nonsmokers and 18.3 microg/day (7.8-32.0) in smokers. In nonsmokers, males had a higher intake than females, 16.6 microg/day (18.6-72.6) and 12.8 microg/day (4.1-30.2), respectively. Nonsmokers had a median AA and GA adduct concentration of 36.8 (range 17.9-65.5) and 18.2 (range 6.7-45.6) pmol/g globin, respectively. In smokers, the values were 165.8 (98.8-211) and 83.2 (29.1-99.0) pmol/g globin, respectively. Using multiple linear regression analysis, a significant positive correlation was found between the AA-Hb adduct concentration and the intake of chips/snacks and crisp bread. GA-Hb adduct did not correlate with consumption of any of the main food groups. Neither AA-Hb nor GA-Hb adduct concentration correlated with total dietary intake of AA as calculated from the reported food intake. Adduct concentrations did not correlate with 24 h urinary excretion of mercapturic acid metabolites of AA and GA in the same subjects reported previously.

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