Felter Susan P, Daston George P, Euling Susan Y, Piersma Aldert H, Tassinari Melissa S
The Procter & Gamble Company , Cincinnati, OH , USA.
Crit Rev Toxicol. 2015 Mar;45(3):219-44. doi: 10.3109/10408444.2014.993919. Epub 2015 Feb 17.
Abstract Over the last couple of decades, the awareness of the potential health impacts associated with early-life exposures has increased. Global regulatory approaches to chemical risk assessment are intended to be protective for the diverse human population including all life stages. However, questions persist as to whether the current testing approaches and risk assessment methodologies are adequately protective for infants and children. Here, we review physiological and developmental differences that may result in differential sensitivity associated with early-life exposures. It is clear that sensitivity to chemical exposures during early-life can be similar, higher, or lower than that of adults, and can change quickly within a short developmental timeframe. Moreover, age-related exposure differences provide an important consideration for overall susceptibility. Differential sensitivity associated with a life stage can reflect the toxicokinetic handling of a xenobiotic exposure, the toxicodynamic response, or both. Each of these is illustrated with chemical-specific examples. The adequacy of current testing protocols, proposed new tools, and risk assessment methods for systemic noncancer endpoints are reviewed in light of the potential for differential risk to infants and young children.
摘要 在过去几十年中,人们对早期生活暴露所带来的潜在健康影响的认识有所提高。全球化学风险评估监管方法旨在保护包括所有生命阶段在内的多样化人群。然而,关于当前的测试方法和风险评估方法是否足以保护婴儿和儿童,仍存在疑问。在此,我们回顾了可能导致与早期生活暴露相关的不同敏感性的生理和发育差异。很明显,早期生活期间对化学暴露的敏感性可能与成年人相似、更高或更低,并且在较短的发育时间范围内可能迅速变化。此外,与年龄相关的暴露差异是总体易感性的一个重要考虑因素。与生命阶段相关的不同敏感性可能反映了对外源生物暴露的毒代动力学处理、毒效动力学反应或两者兼而有之。每个方面都用特定化学物质的例子进行了说明。鉴于婴儿和幼儿面临不同风险的可能性,我们对当前测试方案、新提出的工具以及全身性非癌症终点的风险评估方法的充分性进行了审查。