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Population Toxicokinetic Modeling of Cadmium for Health Risk Assessment

Amzal, Billy (författare)
European Food Safety Author, Assessment Methodol Unit, I-43100 Parma, Italy.
Julin, Bettina (författare)
Karolinska Institutet
Vahter, Marie (författare)
Karolinska Institutet
visa fler...
Wolk, Alicja (författare)
Karolinska Institutet
Johanson, Gunnar (författare)
Karolinska Institutet
Akesson, Agneta (författare)
Karolinska Institutet
visa färre...
Karolinska Institutet European Food Safety Author, Assessment Methodol Unit, I-43100 Parma, Italy (creator_code:org_t)
US DEPT HEALTH HUMAN SCIENCES PUBLIC HEALTH SCIENCE, 2009
2009
Engelska.
Ingår i: Journal of Environmental Health Perspectives. - : US DEPT HEALTH HUMAN SCIENCES PUBLIC HEALTH SCIENCE. - 0091-6765 .- 1552-9924. ; 117:8, s. 1293-1301
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BACKGROUND: Cadmium is a widespread environmental pollutant that has been shown to exert toxic effects on kidney and bones in humans after long-term exposure. Urinary cadmium concentration is considered a good biomarker of accumulated cadmium in kidney, and diet is the main source of cadmium among nonsmokers. OBJECTIVE: Modeling the link between urinary cadmium and dietary cadmium intake is a key step in the risk assessment of long-term cadmium exposure. There is, however, little knowledge on how this link may vary, especially for susceptible population strata. METHODS: We used a large population-based study (the Swedish Mammography Cohort), with repeated dietary intake data covering a period of 20 years, to compare estimated dietary cadmium intake with urinary cadmium concentrations on an individual basis. A modified version of the Nordberg-Kjellstrom model and a one-compartment model were evaluated in terms of their predictions of urinary cadmium. We integrated the models and quantified the between-person variability of cadmium half-life in the population. Finally, sensitivity analyses and Monte Carlo simulations were performed to illustrate how the latter model could serve as a robust tool supporting the risk assessment of cadmium in humans. RESULTS: The one-compartment population model appeared to be an adequate modeling option to link cadmium intake to urinary cadmium and to describe the population variability. We estimated the cadmium half-life to be about 11.6 years, with about 25% population variability. CONCLUSIONS: Population toxicokinetic models can be robust and useful tools for risk assessment of chemicals, because they allow quantification and integration of population variability in toxicokinetics.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Arbetsmedicin och miljömedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Occupational Health and Environmental Health (hsv//eng)

Nyckelord

alternative model development
Bayesian inference
cadmium toxicokinetics
population variability
risk assessment
toxicokinetic models
urinary cadmium

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