Zenick H, Griffith J
Health Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Environ Health Perspect. 1995 Apr;103 Suppl 3(Suppl 3):9-12. doi: 10.1289/ehp.95103s39.
The risk assessment process is described with a focus on the hazard identification and dose-response components. Many of the scientific questions and uncertainties associated with these components are discussed, and the role for biomarkers and specimen banking in supporting these activities are assessed. Under hazard identification, the use of biomarkers in defining and predicting a) biologically adverse events; b) the progression of those events towards disease; and c) the potential for reversibility are explored. Biomarker applications to address high-to-low dose extrapolation and interindividual variability are covered under dose-response assessment. Several potential applications for specimen banking are proposed.
风险评估过程在介绍时重点关注危害识别和剂量反应部分。讨论了与这些部分相关的许多科学问题和不确定性,并评估了生物标志物和样本库在支持这些活动中的作用。在危害识别方面,探讨了生物标志物在定义和预测以下方面的用途:a)生物性不良事件;b)这些事件向疾病的进展;c)可逆性的可能性。在剂量反应评估中涵盖了用于解决高剂量到低剂量外推和个体间变异性的生物标志物应用。还提出了样本库的几种潜在应用。