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Estimating Noncancer Uncertainty Factors: Are Ratios NOAELs Informative?

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  • Kevin P. Brand
  • J Lorenz Rhomberg
  • John S. Evans

Abstract

The prominent role of animal bioassay evidence in environmental regulatory decisions compels a careful characterization of extrapolation uncertainties. In noncancer risk assessment, uncertainty factors are incorporated to account for each of several extrapolations required to convert a bioassay outcome into a putative subthreshold dose for humans. Measures of relative toxicity taken between different dosing regimens, different endpoints, or different species serve as a reference for establishing the uncertainty factors. Ratios of no observed adverse effect levels (NOAELs) have been used for this purpose; statistical summaries of such ratios across sets of chemicals are widely used to guide the setting of uncertainty factors. Given the poor statistical properties of NOAELs, the informativeness of these summary statistics is open to question. To evaluate this, we develop an approach to “calibrate” the ability of NOAEL ratios to reveal true properties of a specified distribution for relative toxicity. A priority of this analysis is to account for dependencies of NOAEL ratios on experimental design and other exogenous factors. Our analysis of NOAEL ratio summary statistics finds (1) that such dependencies are complex and produce pronounced systematic errors and (2) that sampling error associated with typical sample sizes (50 chemicals) is nonnegligible. These uncertainties strongly suggest that NOAEL ratio summary statistics cannot be taken at face value; conclusions based on such ratios reported in well over a dozen published papers should be reconsidered.

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  • Kevin P. Brand & J Lorenz Rhomberg & John S. Evans, 1999. "Estimating Noncancer Uncertainty Factors: Are Ratios NOAELs Informative?," Risk Analysis, John Wiley & Sons, vol. 19(2), pages 295-308, April.
  • Handle: RePEc:wly:riskan:v:19:y:1999:i:2:p:295-308
    DOI: 10.1111/j.1539-6924.1999.tb00406.x
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    References listed on IDEAS

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    1. Lorenz R. Rhomberg & Scott K. Wolff, 1998. "Empirical Scaling of Single Oral Lethal Doses Across Mammalian Species Based on a Large Database," Risk Analysis, John Wiley & Sons, vol. 18(6), pages 741-753, December.
    2. David A. Freedman & Lois Swirsky Gold & Thomas H. Slone, 1993. "How Tautological Are Interspecies Correlations of Carcinogenic Potencies?," Risk Analysis, John Wiley & Sons, vol. 13(3), pages 265-272, June.
    3. Jeffrey C. Swartout & Paul S. Price & Michael L. Dourson & Heather L. Carlson‐Lynch & Russell E. Keenan, 1998. "A Probabilistic Framework for the Reference Dose (Probabilistic RfD)," Risk Analysis, John Wiley & Sons, vol. 18(3), pages 271-282, June.
    4. Curtis C. Travis & Robin K. White, 1988. "Interspecific Scaling of Toxicity Data," Risk Analysis, John Wiley & Sons, vol. 8(1), pages 119-125, March.
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    1. Paul S. Price & Heli M. Hollnagel & Jack M. Zabik, 2009. "Characterizing the Noncancer Toxicity of Mixtures Using Concepts from the TTC and Quantitative Models of Uncertainty in Mixture Toxicity," Risk Analysis, John Wiley & Sons, vol. 29(11), pages 1534-1548, November.
    2. David Pennington & Pierre Crettaz & Annick Tauxe & Lorenz Rhomberg & Kevin Brand & Olivier Jolliet, 2002. "Assessing Human Health Response in Life Cycle Assessment Using ED10s and DALYs: Part 2—Noncancer Effects," Risk Analysis, John Wiley & Sons, vol. 22(5), pages 947-963, October.

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