Krewski D, Crump K S, Farmer J, Gaylor D W, Howe R, Portier C, Salsburg D, Sielken R L, Van Ryzin J
Fundam Appl Toxicol. 1983 May-Jun;3(3):140-60. doi: 10.1016/s0272-0590(83)80075-x.
The assessment of health risks due to low levels of exposure to potential environmental hazards based on the results of toxicological experiments necessarily involves extrapolation of results obtained at relatively high doses to the low dose region of interest. In this paper, different statistical extrapolation procedures which take into account both time-to-response and the presence of competing risks are compared using a large simulated data base. The study was designed to cover a range of plausible dose response models as well as to assess the effects of competing risks, background response, latency and experimental design on the performance of the different extrapolation procedures. It was found that point estimates of risk in the low dose region may differ from the actual risk by a factor of 1000 or more in certain situations, even when precise information on the time of occurrence of the particular lesion of interest is available. Although linearized upper confidence limits on risk can be highly conservative when the underlying dose response curve is sublinear in the low dose region, they were found not to exceed the actual risk in the low dose region by more than a factor of 10 in those cases where the underlying dose response curve was linear at low doses.
基于毒理学实验结果对低水平接触潜在环境危害所致健康风险进行评估时,必然要将在相对高剂量下获得的结果外推至感兴趣的低剂量区域。本文利用一个大型模拟数据库,比较了考虑到反应时间和竞争风险存在的不同统计外推程序。该研究旨在涵盖一系列合理的剂量反应模型,同时评估竞争风险、背景反应、潜伏期和实验设计对不同外推程序性能的影响。研究发现,在某些情况下,即使可获得关于感兴趣的特定病变发生时间的精确信息,低剂量区域风险的点估计值与实际风险仍可能相差1000倍或更多。尽管当基础剂量反应曲线在低剂量区域呈亚线性时,风险的线性化上置信限可能会非常保守,但在基础剂量反应曲线在低剂量下呈线性的那些情况下,发现它们在低剂量区域不超过实际风险的10倍。