Minimal Risk Level Derivation for Cadmium: Acute and Intermediate Duration Exposures.

Obaid Faroon, Sam Keith, Moiz Mumtaz, Patricia Ruiz
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Abstract

The Agency for Toxic Substances and Disease Registry (ATSDR) lists cadmium as one of its priority hazardous substances. The agency conducted a comprehensive literature review of cadmium and used the information to develop a toxicological profile that identified the full range of health effects associated with exposure to cadmium. It included an assessment that identified screening levels, termed health guidance values or minimal risk levels (MRLs), below which adverse health effects are not expected. In this paper, we describe how MRLs for cadmium are derived. For the acute inhalation MRL, the traditional no observed adverse effect level or lowest observed adverse effect level (NOAEL/LOAEL) approach is used; for the oral intermediate MRL, the benchmark dose (BMD) approach is used. MRLs were developed for the most sensitive route-specific end points, other than mortality and cancer that were sufficiently supported and justified by the data. These included an acute duration (1-14 day exposure) inhalation MRL of 0.03 µg Cd/m3 for alveolar histiocytic infiltration and focal inflammation in alveolar septa and an intermediate duration (15-365 day exposure) oral MRL of 0.5 µg Cd/kg/day for decreased bone mineral density.

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镉的最小风险水平推导:急性和中期持续暴露。
有毒物质和疾病登记处(ATSDR)将镉列为其优先危险物质之一。该机构对镉进行了全面的文献审查,并利用这些信息制定了一份毒理学概况,确定了与接触镉有关的所有健康影响。其中包括一项评估,确定了被称为健康指导值或最低风险水平的筛查水平,低于这些水平预计不会对健康产生不利影响。在本文中,我们描述了镉的MRLs是如何得到的。对于急性吸入性MRL,采用传统的无观察到不良反应水平或最低观察到不良反应水平(NOAEL/LOAEL)方法;对于口服中间MRL,采用基准剂量(BMD)方法。MRLs是针对最敏感的特定途径的终点制定的,而不是死亡率和癌症,这些数据得到充分支持和证明。其中包括急性期(1-14天暴露)吸入MRL为0.03µg Cd/m3,导致肺泡组织细胞浸润和肺泡间隔局灶性炎症,中期(15-365天暴露)口服MRL为0.5µg Cd/kg/天,导致骨密度降低。
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