Science Inventory

Evaluating MoE and its Uncertainty and Variability for Food Contaminants (EuroTox presentation)

Citation:

Setzer, Woodrow. Evaluating MoE and its Uncertainty and Variability for Food Contaminants (EuroTox presentation). Presented at EuroTox 2014, Edinburgh, SCOTLAND, September 07 - 10, 2014. https://doi.org/10.23645/epacomptox.5080285

Impact/Purpose:

Margin of Exposure (MoE) is a metric for quantifying the relationship between exposure and hazard. It is a ratio of estimated doses, and characterizing the uncertainty and variability of a MoE requires characterizations for the numerator and denominator. New methodologies for high-throughput assessment may substantially broaden the applicability.

Description:

Margin of Exposure (MoE), is a metric for quantifying the relationship between exposure and hazard. Ideally, it is the ratio of the dose associated with hazard and an estimate of exposure. For example, hazard may be characterized by a benchmark dose (BMD), and, for food contaminants, exposure by a measure of ingested chemical in the same units (say, mg/kg/day). Generally, both measures are uncertain, and may vary based on lifestyle and differ between children and adults. Use of BMD rather than NOAELs or T25 to characterize hazard is more appropriate when computing the MoE because the BMD is well-defined, can be efficiently calculated from typical bioassay data, and statistical methods for characterizing its uncertainty are relatively mature. However, for most chemicals there is substantially greater uncertainty in the denominator of the MoE. Available modeling approaches show promise, but often require substantial effort to parameterize. One challenge to the MoE approach is the limited availability of empirical hazard data for most chemicals. Promising new technologies are being developed to solve this data gap. This includes the US EPA’s ExpoCast program which enables prediction of exposure estimates for thousands of chemicals based on use and production. In addition, reverse toxicokinetics (rTK) and in vitro to in vivo predictive models are connecting in vitro hazard concentrations to daily exposure estimates. New models and methods like these show great promise in reducing uncertainties in risk estimates for data poor chemcials. This abstract does not necessarily reflect U.S. EPA policy.

Record Details:

Record Type:DOCUMENT( PRESENTATION/ SLIDE)
Product Published Date:09/08/2014
Record Last Revised:11/24/2014
OMB Category:Other
Record ID: 293933