During the previous years of the Superfund project it has become obvious that there is a need for a rigorous modeling framework that it will permit the integrated analysis of environmental fate, exposure to pollutants and the resulting health impacts (on the individual receptor and the population levels). In fact, the issue of how to develop and apply efficiently such a modeling framework is one of the most important outstanding questions in current human exposure analysis and risk assessment. In this project we propose a holistochastic Bayesian maximum entropy (BME) framework to model the spatiotemporal distribution of environmental fate and resulting pollutants and to investigate the effects on the exposed population (the term """"""""holistic"""""""" implies a human exposure whole that has a reality greater than the sum of its parts environmental fate, exposure, health effects, etc.; the term """"""""stochastic"""""""" denotes that as a result of the physical variations and biological uncertainties involved at every stage, we need to employ a probablistic characterization of human exposure). It is our intention to develop a very general and flexible modeling framework that covers a wide variety of pollutant distributions and involves a feedback process to facilitate that necessary changes as more is covered about human exposure in the future. The BME framework allows the horizontal integration among sciences related to the human exposure problem that leads to accurate and informative spatiotemporal maps of exposure and effect distributions and an integrative analysis of the whole risk case. By processing a variety of knowledge bases, BME can bring together several sciences which are relevant to the aspect of human exposure reality that is examined. Risk assessment issues will be addressed integratively and interactively within the BME framework. While developing the BME modeling framework, particular emphasis will be given to establishing a working environment where human exposure modeling and laboratory (or field) research are integrate with each other in a meaningful way. BME is thus a central component of an interdisciplinary effort to model environmental health systems which involve natural variables, exposure mechanisms, biological processes, physiology parameters, and epidemiological indicators. In this context, holistochastic BME is a vital component of human exposure analysis and scientific risk assessment.

Project Start
2002-04-01
Project End
2003-03-31
Budget Start
Budget End
Support Year
11
Fiscal Year
2002
Total Cost
$175,236
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Balik-Meisner, Michele; Truong, Lisa; Scholl, Elizabeth H et al. (2018) Elucidating Gene-by-Environment Interactions Associated with Differential Susceptibility to Chemical Exposure. Environ Health Perspect 126:067010
To, Kimberly T; Fry, Rebecca C; Reif, David M (2018) Characterizing the effects of missing data and evaluating imputation methods for chemical prioritization applications using ToxPi. BioData Min 11:10
Dalaijamts, Chimeddulam; Cichocki, Joseph A; Luo, Yu-Syuan et al. (2018) Incorporation of the glutathione conjugation pathway in an updated physiologically-based pharmacokinetic model for perchloroethylene in mice. Toxicol Appl Pharmacol 352:142-152
Gray, Kathleen M (2018) From Content Knowledge to Community Change: A Review of Representations of Environmental Health Literacy. Int J Environ Res Public Health 15:
Li, Gen; Jima, Dereje; Wright, Fred A et al. (2018) HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues. BMC Bioinformatics 19:95
Adebambo, Oluwadamilare A; Shea, Damian; Fry, Rebecca C (2018) Cadmium disrupts signaling of the hypoxia-inducible (HIF) and transforming growth factor (TGF-?) pathways in placental JEG-3 trophoblast cells via reactive oxygen species. Toxicol Appl Pharmacol 342:108-115
Smeester, Lisa; Fry, Rebecca C (2018) Long-Term Health Effects and Underlying Biological Mechanisms of Developmental Exposure to Arsenic. Curr Environ Health Rep 5:134-144
Luo, Yu-Syuan; Furuya, Shinji; Chiu, Weihsueh et al. (2018) Characterization of inter-tissue and inter-strain variability of TCE glutathione conjugation metabolites DCVG, DCVC, and NAcDCVC in the mouse. J Toxicol Environ Health A 81:37-52
Singleton, David R; Lee, Janice; Dickey, Allison N et al. (2018) Polyphasic characterization of four soil-derived phenanthrene-degrading Acidovorax strains and proposal of Acidovorax carolinensis sp. nov. Syst Appl Microbiol 41:460-472
Luo, Yu-Syuan; Hsieh, Nan-Hung; Soldatow, Valerie Y et al. (2018) Comparative analysis of metabolism of trichloroethylene and tetrachloroethylene among mouse tissues and strains. Toxicology 409:33-43

Showing the most recent 10 out of 505 publications