中间效应生物标志物——直接浓度的替代品——用于监管效益分析的响应数据

D. Hattis
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引用次数: 0

摘要

人们认为需要获得广泛的特定化学品毒理学信息,这阻碍了评估危险空气污染物可能标准的风险和评估可能对公众健康的保护益处的努力。本文讨论了利用HAPs对早期效应生物标志物(如出生体重)的影响来预测罕见的量子效应的可能变化的机会,这将与减少暴露可能带来的监管效益的量化相关。在出生体重的例子中,即使是适度暴露在常见的空气污染物中,也会被视为对胎儿生长发育的有限资源产生一种税收。与致畸效应相反,动物胎儿生长受限的剂量反应关系通常接近线性,这表明发育中的胎儿可能通常没有未开发的“功能储备能力”,而传统毒理学范式认为,这种能力有望缓冲适度暴露于毒物的影响。鉴于这一机制观点,并部分得到所报告的吸烟与出生体重和婴儿死亡率之间平行剂量反应关系的支持,限制胎儿生长可能与在流行病学研究中更难以直接评估的所关注的数量末端效应的变化有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermediate Effect Biomarkers--Alternatives to Direct Concentration- Response Data for Regulatory Benefits Analyses
Perceived needs for extensive chemical-specific toxicological information have impeded efforts to assess risks and evaluate likely public health protection benefits of possible standards for hazardous air pollutants (HAPs). This paper discusses opportunities to use effects of HAPs on early effect biomarkers, such as birth weights, to predict likely changes in rare quantal effects of concern that would be relevant for the quantification of likely regulatory benefits from exposure reductions. In the birth weight example, even modest exposures to common air pollutants can be seen as producing a kind of tax on the limited resources available to the fetus to grow and develop. In contrast to teratogenic effects, dose response relationships for fetal growth restriction in animals are often nearly linear, suggesting that the developing fetus may not generally have untapped "functional reserve capacity" that is expected to buffer the effects of modest exposures to toxicants in the traditional toxicological paradigm. Given this mechanistic perspective, supported in part by parallel dose response relationships between reported cigarette smoking and both birth weight and infant mortality, restriction on fetal growth can be associated with changes in quantal end effects of concern that are more difficult to assess directly in epidemiological studies.
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