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Human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data

  • Yanying Ma
  • , Camilla Taxvig
  • , Andrea Rodríguez-Carrillo
  • , Vicente Mustieles
  • , Lena Reiber
  • , Anja Kiesow
  • , Nathalie Michelle Löbl
  • , Mariana F. Fernández
  • , Tina Vicky Alstrup Hansen
  • , Maria João Valente
  • , Marike Kolossa-Gehring
  • , Madlen David
  • , Anne Marie Vinggaard*
  • *Corresponding author for this work
  • University of Granada
  • German Environment Agency

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

Background: Scientific evidence for underestimated toxicity from unintentional exposure to chemical mixtures is mounting. Yet, harmonized approaches on how to assess the actual risk of mixtures is lacking. As part of the European Joint programme ‘Human Biomonitoring for Europe’ we explored a novel methodology for mixture risk assessment of chemicals affecting male reproductive function.

Methodology:
We explored a methodology for chemical mixture risk assessment based on human in vitro data combined with human exposure data, thereby circumventing the drawbacks of using hazard data from rodents and estimated exposure intake levels. Human androgen receptor (hAR) antagonism was selected as the most important molecular initiating event linked to adverse outcomes on male reproductive health.

Results:
Our work identified 231 chemicals able to interfere with hAR activity. Among these were 61 finally identified as having both reliable hAR antagonist and human biomonitoring data. Calculation of risk quotients indicated that PCBs (118, 138, 157), phthalates (BBP, DBP, DIBP), benzophenone-3, PFOS, methylparaben, triclosan, some pesticides (i.e cypermethrin, β-endosulfan, methylparathion, p,p-DDE), and a PAH metabolite (1-hydroxypyrene) contributed to the mixture effect. The major chemical mixture drivers were PCB 118, BBP, PFOS, DBP, and the UV filter benzophenone-3, together contributing with 75% of the total mixture effect that was primarily driven by high exposure values

Conclusions:
This viable way forward for mixture risk assessment of chemicals has the advantages of 1) being a more comprehensive mixture risk assessment also covering data-poor chemicals, and 2) including human data only. However, the approach is subjected to uncertainties in terms of in vitro to in vivo extrapolation, it is not ready for decision making, and needs further development. Still, the results indicate a concern for adverse effects on reproductive function in highly exposed boys, especially when considering additional exposure to data-poor chemicals and chemicals acting by other mechanisms of action.
Original languageEnglish
Article number107815
JournalEnvironment International
Volume173
Number of pages14
ISSN0160-4120
DOIs
Publication statusPublished - 2023

Bibliographical note

The authors thank the European Union’s Horizon 2020 research and innovation programme HBM4EU under Grant Agreement No. 733032 and the Green Deal project PANORAMIX Grant Agreement No. 101036631 for its financial support.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Chemical mixture risk assessment
  • Human risk
  • Antiandrogenic chemicals
  • Human biomonitoring data
  • Androgen receptor antagonism

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