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Incorporating regulatory guideline values in analysis of epidemiology data.
Gennings, Chris; Shu, Huan; Rudén, Christina; Öberg, Mattias; Lindh, Christian; Kiviranta, Hannu; Bornehag, Carl-Gustaf.
Afiliação
  • Gennings C; Dept of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: chris.gennings@mssm.edu.
  • Shu H; Stockholm University, Stockholm, Sweden.
  • Rudén C; Stockholm University, Stockholm, Sweden.
  • Öberg M; Swedish Toxicology Sciences Research Center (Swetox), Karolinska Institute, Södertälje, Sweden.
  • Lindh C; Lund University, Lund, Sweden.
  • Kiviranta H; National Institute of Health and Welfare, Helsinki, Finland.
  • Bornehag CG; Dept of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Dept of Health Sciences, Karlstad University, Karlstad, Sweden.
Environ Int ; 120: 535-543, 2018 11.
Article em En | MEDLINE | ID: mdl-30170308
ABSTRACT
Fundamental to regulatory guidelines is to identify chemicals that are implicated with adverse human health effects and inform public health risk assessors about "acceptable ranges" of such environmental exposures (e.g., from consumer products and pesticides). The process is made more difficult when accounting for complex human exposures to multiple environmental chemicals. Herein we propose a new class of nonlinear statistical models for human data that incorporate and evaluate regulatory guideline values into analyses of health effects of exposure to chemical mixtures using so-called 'desirability functions' (DFs). The DFs are incorporated into nonlinear regression models to allow for the simultaneous estimation of points of departure for risk assessment of combinations of individual substances that are parts of chemical mixtures detected in humans. These are, in contrast to published so-called biomonitoring equivalent (BE) values and human biomonitoring (HBM) values that link regulatory guideline values from in vivo studies of single chemicals to internal concentrations monitored in humans. We illustrate the strategy through the analysis of prenatal concentrations of mixtures of 11 chemicals with suspected endocrine disrupting properties and two health effects birth weight and language delay at 2.5 years. The strategy allows for the creation of a Mixture Desirability Function i.e., MDF, which is a uni-dimensional construct of the set of single chemical DFs; thus, it focuses the resulting inference to a single dimension for a more powerful one degree-of-freedom test of significance. Based on the application of this new method we conclude that the guideline values need to be lower than those for single chemicals when the chemicals are observed in combination to achieve a similar level of protection as was aimed for the individual chemicals. The proposed modeling may thus suggest data-driven uncertainty factors for single chemical risk assessment that takes environmental mixtures into account.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Substâncias Perigosas / Modelos Estatísticos / Misturas Complexas / Exposição Ambiental / Disruptores Endócrinos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Substâncias Perigosas / Modelos Estatísticos / Misturas Complexas / Exposição Ambiental / Disruptores Endócrinos Idioma: En Ano de publicação: 2018 Tipo de documento: Article