Department of Mathematics and Statistics, Louisiana Tech University, Ruston, Louisiana 71272-0046, USA.
Crit Rev Toxicol. 2011 Sep;41(8):637-50. doi: 10.3109/10408444.2011.566258. Epub 2011 Jun 30.
Under current guidelines, exposure guidelines for toxicants are determined by following one of two different tracks depending on whether the toxicant's mode of action (MOA) is believed to involve an exposure threshold. Although not denying the existence of thresholds, this paper points out problems with how the threshold concept and MOA is used in risk assessment. Thresholds are frequently described using imprecise terms that imply some unspecified increase in risk, which robs them of any meaning (any reasonable dose response will satisfy such a definition) and tacitly implies a value judgment about how large a risk is acceptable. MOA is generally used only to inform a threshold's existence and not its value. Often MOA is used only to conclude that the adverse effect requires an upstream cellular or biochemical response for which a threshold is simply assumed. Data to inform MOA often come from animals, which complicates evaluation of the role of human variation in genetic and environmental conditions, and the possible interaction of the toxicant with processes already producing background toxicity in humans. In response to these and other problems with the current two-track approach, this paper proposes a modified point of departure/safety factor approach to setting exposure guidelines for all toxicants. MOA and the severity of the toxic effect would be addressed using safety factors calculated from guidelines established by consensus and based on scientific judgment. The method normally would not involve quantifying low-dose risk, and would not require a threshold determination, although MOA information regarding the likelihood of a threshold could be used in setting safety factors.
根据现行指南,如果认为有毒物质的作用模式 (MOA) 涉及暴露阈值,则根据以下两种不同途径之一确定有毒物质的暴露指南。本文虽然不否认阈值的存在,但指出了在风险评估中使用阈值概念和 MOA 存在的问题。阈值经常使用不精确的术语来描述,这些术语暗示存在某种未指定的风险增加,从而使它们失去了任何意义(任何合理的剂量反应都将满足这种定义),并含蓄地暗示了对可接受风险大小的价值判断。MOA 通常仅用于告知阈值的存在,而不告知其值。通常,MOA 仅用于得出不良影响需要上游细胞或生化反应的结论,而阈值只是假设。用于告知 MOA 的数据通常来自动物,这增加了评估人类遗传和环境条件变化以及有毒物质与已经在人类中产生背景毒性的过程相互作用的可能性。针对当前双轨方法存在的这些和其他问题,本文提出了一种修改的起点/安全系数方法,用于为所有有毒物质制定暴露指南。使用从共识制定并基于科学判断的指南计算的安全系数来解决 MOA 和有毒作用的严重程度。该方法通常不会涉及量化低剂量风险,也不需要确定阈值,尽管关于阈值可能性的 MOA 信息可用于设置安全系数。