Approaches to advancing quantitative human health risk assessment of environmental chemicals in the post-genomic era

被引:15
作者
Chiu, Weihsueh A. [1 ]
Euling, Susan Y. [1 ]
Scott, Cheryl Siegel [1 ]
Subramaniam, Ravi P. [1 ]
机构
[1] US EPA, Natl Ctr Environm Assessment, Washington, DC 20460 USA
关键词
Toxicogenomics; Biomarkers; Molecular epidemiology; Risk assessment; Dose-response assessment; FEMALE REPRODUCTIVE-SYSTEM; INDUCED RESPIRATORY CANCER; GENE-EXPRESSION; POPULATION-DISTRIBUTION; DOSE-RESPONSE; 17-ALPHA-ETHYNYL ESTRADIOL; INHALED FORMALDEHYDE; 21ST-CENTURY IMPLICATIONS; SENSITIVITY-ANALYSIS; WIDE ASSOCIATION;
D O I
10.1016/j.taap.2010.03.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The contribution of genomics and associated technologies to human health risk assessment for environmental chemicals has focused largely on elucidating mechanisms of toxicity, as discussed in other articles in this issue. However, there is interest in moving beyond hazard characterization to making more direct impacts on quantitative risk assessment (QRA) - i.e., the determination of toxicity values for setting exposure standards and cleanup values. We propose that the evolution of QRA of environmental chemicals in the post-genomic era will involve three, somewhat overlapping phases in which different types of approaches begin to mature. The initial focus (in Phase I) has been and continues to be on "augmentation" of weight of evidence using genomic and related technologies qualitatively to increase the confidence in and scientific basis of the results of QRA. Efforts aimed towards "integration" of these data with traditional animal-based approaches, in particular quantitative predictors, or surrogates, for the in vivo toxicity data to which they have been anchored are just beginning to be explored now (in Phase II). In parallel, there is a recognized need for "expansion" of the use of established biomarkers of susceptibility or risk of human diseases and disorders for QRA, particularly for addressing the issues of cumulative assessment and population risk. Ultimately (in Phase III), substantial further advances could be realized by the development of novel molecular and pathway-based biomarkers and statistical and in silica models that build on anticipated progress in understanding the pathways of human diseases and disorders. Such efforts would facilitate a gradual "reorientation" of QRA towards approaches that more directly link environmental exposures to human outcomes. Published by Elsevier Inc.
引用
收藏
页码:309 / 323
页数:15
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