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Model Averaging in Microbial Risk Assessment Using Fractional Polynomials

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  • Harriet Namata
  • Marc Aerts
  • Christel Faes
  • Peter Teunis

Abstract

The alleviation of food‐borne diseases caused by microbial pathogen remains a great concern in order to ensure the well‐being of the general public. The relation between the ingested dose of organisms and the associated infection risk can be studied using dose‐response models. Traditionally, a model selected according to a goodness‐of‐fit criterion has been used for making inferences. In this article, we propose a modified set of fractional polynomials as competitive dose‐response models in risk assessment. The article not only shows instances where it is not obvious to single out one best model but also illustrates that model averaging can best circumvent this dilemma. The set of candidate models is chosen based on biological plausibility and rationale and the risk at a dose common to all these models estimated using the selected models and by averaging over all models using Akaike's weights. In addition to including parameter estimation inaccuracy, like in the case of a single selected model, model averaging accounts for the uncertainty arising from other competitive models. This leads to a better and more honest estimation of standard errors and construction of confidence intervals for risk estimates. The approach is illustrated for risk estimation at low dose levels based on Salmonella typhi and Campylobacter jejuni data sets in humans. Simulation studies indicate that model averaging has reduced bias, better precision, and also attains coverage probabilities that are closer to the 95% nominal level compared to best‐fitting models according to Akaike information criterion.

Suggested Citation

  • Harriet Namata & Marc Aerts & Christel Faes & Peter Teunis, 2008. "Model Averaging in Microbial Risk Assessment Using Fractional Polynomials," Risk Analysis, John Wiley & Sons, vol. 28(4), pages 891-905, August.
  • Handle: RePEc:wly:riskan:v:28:y:2008:i:4:p:891-905
    DOI: 10.1111/j.1539-6924.2008.01063.x
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    References listed on IDEAS

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    1. A. John Bailer & Robert B. Noble & Matthew W. Wheeler, 2005. "Model Uncertainty and Risk Estimation for Experimental Studies of Quantal Responses," Risk Analysis, John Wiley & Sons, vol. 25(2), pages 291-299, April.
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    3. Patrick Royston & Douglas G. Altman, 1994. "Regression Using Fractional Polynomials of Continuous Covariates: Parsimonious Parametric Modelling," Journal of the Royal Statistical Society Series C, Royal Statistical Society, vol. 43(3), pages 429-453, September.
    4. Matthew W. Wheeler & A. John Bailer, 2007. "Properties of Model‐Averaged BMDLs: A Study of Model Averaging in Dichotomous Response Risk Estimation," Risk Analysis, John Wiley & Sons, vol. 27(3), pages 659-670, June.
    5. P. F. M. Teunis & A. H. Havelaar, 2000. "The Beta Poisson Dose‐Response Model Is Not a Single‐Hit Model," Risk Analysis, John Wiley & Sons, vol. 20(4), pages 513-520, August.
    6. Hojin Moon & Hyun‐Joo Kim & James J. Chen & Ralph L. Kodell, 2005. "Model Averaging Using the Kullback Information Criterion in Estimating Effective Doses for Microbial Infection and Illness," Risk Analysis, John Wiley & Sons, vol. 25(5), pages 1147-1159, October.
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    2. Steven B. Kim & Ralph L. Kodell & Hojin Moon, 2014. "A Diversity Index for Model Space Selection in the Estimation of Benchmark and Infectious Doses via Model Averaging," Risk Analysis, John Wiley & Sons, vol. 34(3), pages 453-464, March.
    3. Vegard Nilsen & John Wyller, 2016. "QMRA for Drinking Water: 1. Revisiting the Mathematical Structure of Single‐Hit Dose‐Response Models," Risk Analysis, John Wiley & Sons, vol. 36(1), pages 145-162, January.
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    5. Hojin Moon & Steven B. Kim & James J. Chen & Nysia I. George & Ralph L. Kodell, 2013. "Model Uncertainty and Model Averaging in the Estimation of Infectious Doses for Microbial Pathogens," Risk Analysis, John Wiley & Sons, vol. 33(2), pages 220-231, February.

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