Mathematical modelling and quantitative methods

被引:79
作者
Edler, L
Poirier, K
Dourson, M
Kleiner, J
Mileson, B
Nordmann, H
Renwick, A
Slob, W
Walton, K
Würtzen, G
机构
[1] ILSI Europe, B-1200 Brussels, Belgium
[2] German Canc Res Ctr, Deutsch Krebsforschungszentrum, Biostat Abt, D-69009 Heidelberg, Germany
[3] TERA, Toxicol Excellence Risk Assessment, Cincinnati, OH 45223 USA
[4] Technol Sci Grp Inc, Toxicol Ecotoxicol & Risk Assessment Div, Washington, DC 20036 USA
[5] Aiinomoto Switzerland AG, CH-6304 Zug, Switzerland
[6] Univ Southampton, Clin Pharmacol Grp, Southampton SO16 7PX, Hants, England
[7] Natl Inst Publ Hlth & Environm, RIVM, NL-3720 BA Bilthoven, Netherlands
[8] Coca Cola Nord & Balt, DK-2900 Copenhagen, Denmark
关键词
hazard characterisations; risk assessment; mathematical modelling; benchmark; probabilistic methods; toxicokinetic models; categorical regression;
D O I
10.1016/S0278-6915(01)00116-8
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The present review reports on the mathematical methods and statistical techniques presently available for hazard characterisation. The state of the art of mathematical modelling and quantitative methods used currently for regulatory decision-making in Europe and additional potential methods for risk assessment of chemicals in food and diet are described. Existing practices of JECFA. FDA. EPA. etc.. are examined for their similarities and differences. A framework is established for the development of new and improved quantitative methodologies. Areas for refinement. improvement and increase of efficiency of each method are identified in a gap analysis. Based on this critical evaluation, needs for future research are defined. It is concluded from our work that mathematical modelling of the dose response relationship would improve the risk assessment process, An adequate characterisation of the dose response relationship by mathematical modelling clearly requires the use of a sufficient number of dose groups to achieve a range of different response levels, This need not necessarily lead to an increase in the total number of animals in the study if an appropriate design is used. Chemical-specific data relating to the mode or mechanism of action and/or the toxicokinetics of the chemical should be used for dose response characterisation whenever possible. It is concluded that a single method of hazard characterisation would not be suitable for all kinds of risk assessments, and that a range of different approaches is necessary so that the method used is the most appropriate for the data available and for the risk characterisation issue. Future refinements to dose-response characterisation should incorporate more clearly the extent of uncertainty and variability in the resulting output. (C) 2002 ILSI. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:283 / 326
页数:44
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