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剂量反应特征描述:I:基准剂量概念的批判性评估

Characterizing dose-response: I: Critical assessment of the benchmark dose concept.

作者信息

Murrell J A, Portier C J, Morris R W

机构信息

Analytical Sciences, Inc., Durham, North Carolina, USA.

出版信息

Risk Anal. 1998 Feb;18(1):13-26. doi: 10.1111/j.1539-6924.1998.tb00911.x.

DOI:10.1111/j.1539-6924.1998.tb00911.x
PMID:9523441
Abstract

We present a critical assessment of the benchmark dose (BMD) method introduced by Crump as an alternative method for setting a characteristic dose level for toxicant risk assessment. The no-observed-adverse-effect-level (NOAEL) method has been criticized because it does not use all of the data and because the characteristic dose level obtained depends on the dose levels and the statistical precision (sample sizes) of the study design. Defining the BMD in terms of a confidence bound on a point estimate results in a characteristic dose that also varies with the statistical precision and still depends on the study dose levels. Indiscriminate choice of benchmark response level may result in a BMD that reflects little about the dose-response behavior available from using all of the data. Another concern is that the definition of the BMD for the quantal response case is different for the continuous response case. Specifically, defining the BMD for continuous data using a ratio of increased effect divided by the background response results in an arbitrary dependence on the natural background for the endpoint being studied, making comparison among endpoints less meaningful and standards more arbitrary. We define a modified benchmark dose as a point estimate using the ratio of increased effect divided by the full adverse response range which enables consistent placement of the benchmark response level and provides a BMD with a more consistent relationship to the dose-response curve shape.

摘要

我们对Crump提出的基准剂量(BMD)方法进行了批判性评估,该方法作为设定毒物风险评估特征剂量水平的一种替代方法。未观察到不良反应水平(NOAEL)方法受到了批评,因为它没有使用所有数据,而且所获得的特征剂量水平取决于研究设计的剂量水平和统计精度(样本量)。根据点估计的置信区间来定义BMD会导致特征剂量也随统计精度而变化,并且仍然依赖于研究剂量水平。随意选择基准反应水平可能会导致一个BMD,它几乎无法反映使用所有数据所得到的剂量反应行为。另一个问题是,对于定量反应情况的BMD定义与连续反应情况不同。具体而言,使用效应增加量与背景反应的比值来定义连续数据的BMD会导致对所研究终点的自然背景产生任意依赖,使得不同终点之间的比较意义不大,标准也更加随意。我们将修正的基准剂量定义为使用效应增加量与完全不良反应范围的比值的点估计,这能够一致地确定基准反应水平,并提供一个与剂量反应曲线形状具有更一致关系的BMD。

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