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

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 m...

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Autores principales: Ma, Yanying, Taxvig, Camilla, Rodríguez-Carrillo, Andrea, Mustieles, Vicente, Reiber, Lena, Kiesow, Anja, Löbl, Nathalie Michelle, Fernández, Mariana F., Hansen, Tina Vicky Alstrup, Valente, Maria João, Kolossa-Gehring, Marike, David, Madlen, Vinggaard, Anne Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030311/
https://www.ncbi.nlm.nih.gov/pubmed/36822008
http://dx.doi.org/10.1016/j.envint.2023.107815
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author Ma, Yanying
Taxvig, Camilla
Rodríguez-Carrillo, Andrea
Mustieles, Vicente
Reiber, Lena
Kiesow, Anja
Löbl, Nathalie Michelle
Fernández, Mariana F.
Hansen, Tina Vicky Alstrup
Valente, Maria João
Kolossa-Gehring, Marike
David, Madlen
Vinggaard, Anne Marie
author_facet Ma, Yanying
Taxvig, Camilla
Rodríguez-Carrillo, Andrea
Mustieles, Vicente
Reiber, Lena
Kiesow, Anja
Löbl, Nathalie Michelle
Fernández, Mariana F.
Hansen, Tina Vicky Alstrup
Valente, Maria João
Kolossa-Gehring, Marike
David, Madlen
Vinggaard, Anne Marie
author_sort Ma, Yanying
collection PubMed
description 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.
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spelling pubmed-100303112023-03-23 Human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data Ma, Yanying Taxvig, Camilla Rodríguez-Carrillo, Andrea Mustieles, Vicente Reiber, Lena Kiesow, Anja Löbl, Nathalie Michelle Fernández, Mariana F. Hansen, Tina Vicky Alstrup Valente, Maria João Kolossa-Gehring, Marike David, Madlen Vinggaard, Anne Marie Environ Int Full Length Article 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. Elsevier Science 2023-03 /pmc/articles/PMC10030311/ /pubmed/36822008 http://dx.doi.org/10.1016/j.envint.2023.107815 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Ma, Yanying
Taxvig, Camilla
Rodríguez-Carrillo, Andrea
Mustieles, Vicente
Reiber, Lena
Kiesow, Anja
Löbl, Nathalie Michelle
Fernández, Mariana F.
Hansen, Tina Vicky Alstrup
Valente, Maria João
Kolossa-Gehring, Marike
David, Madlen
Vinggaard, Anne Marie
Human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data
title Human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data
title_full Human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data
title_fullStr Human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data
title_full_unstemmed Human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data
title_short Human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data
title_sort human risk associated with exposure to mixtures of antiandrogenic chemicals evaluated using in vitro hazard and human biomonitoring data
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030311/
https://www.ncbi.nlm.nih.gov/pubmed/36822008
http://dx.doi.org/10.1016/j.envint.2023.107815
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