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Published on: May 13, 2020
Dioxin health risk to infants using simulated tissue concentrations
Wakae Maruyama1, Kikuo Yoshida, Yasunobu Aoki
1Research Center for Environmental Risk, National Institute for Environmental Studies,16-2 Onogawa, Tsukuba 305-8506, Japan.
Insights
Physiologically based pharmacokinetic (PBPK) models simulated dioxin levels in infants. Breast-fed infants had higher liver dioxin concentrations, indicating potential risks requiring further study.
Area of Science:
- Environmental Health
- Toxicology
- Pharmacokinetics
Background:
- Dioxin exposure in infants and children is a public health concern.
- Understanding dioxin pharmacokinetics is crucial for risk assessment.
Purpose of the Study:
- To simulate dioxin concentrations in infant and child populations using PBPK models.
- To assess potential health risks associated with dioxin exposure in infants.
Main Methods:
- Development and validation of PBPK models for infant and child populations.
- Simulation of temporal dioxin concentration patterns in various tissues.
- Calculation of toxic equivalency (TEQ) for dioxin mixtures in the liver.
Main Results:
- PBPK infant model showed good agreement with literature data.
- Simulated maximum liver concentrations were 16.8 pg TEQ/g in breast-fed and 3.5 pg TEQ/g in formula-fed infants.
- Breast-fed infant liver concentrations were significantly lower than levels associated with adverse health effects in animal models.
Conclusions:
- Current dioxin contamination levels may pose risks to infants.
- Further dose-response data is needed for a comprehensive quantitative risk assessment.
Abstract:
Dioxin concentrations in infant and child were simulated using physiologically based pharmacokinetic (PBPK) models developed for these groups. The infant model was validated by comparing the simulated concentration with the measured concentration from the literature, and they showed good agreement. Simulations with our PBPK model showed temporal patterns in concentrations in various tissues. For risk assessment, estimated concentrations of 29 dioxins in the liver were summed up in a toxic equivalency (TEQ) basis to be compared with actual 2,3,7,8-TCDD concentrations in rat liver associated with toxicity. Maximum liver concentrations in breast-fed and formula-fed infants were 16.8pg TEQ/g and 3.5pg TEQ/g, respectively. The level in breast-fed infant liver was approximately 1/300 of the level associated with hepatocellular carcinoma and 1/5 of the level found in maternal rat liver associated with alterations in reproductive organs in the next generation. Based on our analysis, the present contamination level is not safe enough, but further dose-response data is required for a quantitative risk assessment.
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