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Assessment of the endocrine disrupting properties of bisphenol AF: a case study applying the European regulatory criteria and guidance
BACKGROUND: Scientific criteria to identify endocrine disruptors (ED) was recently implemented for plant protection products (PPP) and biocidal products (BP). A guidance document has been published by ECHA and EFSA in the context of ED criteria for PPPs and BPs. METHODS: In the present work, a case...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070297/ https://www.ncbi.nlm.nih.gov/pubmed/33894771 http://dx.doi.org/10.1186/s12940-021-00731-0 |
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author | Escrivá, Laura Zilliacus, Johanna Hessel, Ellen Beronius, Anna |
author_facet | Escrivá, Laura Zilliacus, Johanna Hessel, Ellen Beronius, Anna |
author_sort | Escrivá, Laura |
collection | PubMed |
description | BACKGROUND: Scientific criteria to identify endocrine disruptors (ED) was recently implemented for plant protection products (PPP) and biocidal products (BP). A guidance document has been published by ECHA and EFSA in the context of ED criteria for PPPs and BPs. METHODS: In the present work, a case study was performed on Bisphenol AF (BPAF) to explore the application of the EU criteria and EFSA/ECHA guidance document for the ED assessment of a non-pesticide chemical regulated under REACH. A data dossier was built by a systematic literature search (Web of Science, Pubmed, Embase; n = 511), title/abstract screening (n = 124) and full text examination (n = 88). All the information was extracted and systematically reported for 309 parameters (100 for adversity; 209 for endocrine activity). The reliability of studies was assessed (SciRAP tool). RESULTS: Data were synthesized into 96 lines of evidence for adversity (n = 57), and endocrine activity (n = 39); and assessed by weight of evidence methodology. The initial analysis of the evidence indicated EATS-mediated adversity in mammals, therefore a mode of action (MoA) was postulated for both male and female adult exposure. Female MoA included estrogen receptor activation and altered steroidogenesis leading to ovarian dysfunction, altered estrous cycling and impaired female fertility. Male MoA was initiated by androgen receptor inhibition and altered steroidogenesis leading to dysfunction of male reproductive organs and impaired male fertility. CONCLUSIONS: The overall conclusion of the ED assessment indicated that BPAF meets the ED criteria for human health. The steps described in the ED guidance document were successfully completed, resulting in a thorough, structured and transparent identification of BPAF as an ED. Advantages and limitations of applying the ED criteria and guidance for a REACH chemical are discussed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12940-021-00731-0. |
format | Online Article Text |
id | pubmed-8070297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80702972021-04-26 Assessment of the endocrine disrupting properties of bisphenol AF: a case study applying the European regulatory criteria and guidance Escrivá, Laura Zilliacus, Johanna Hessel, Ellen Beronius, Anna Environ Health Research BACKGROUND: Scientific criteria to identify endocrine disruptors (ED) was recently implemented for plant protection products (PPP) and biocidal products (BP). A guidance document has been published by ECHA and EFSA in the context of ED criteria for PPPs and BPs. METHODS: In the present work, a case study was performed on Bisphenol AF (BPAF) to explore the application of the EU criteria and EFSA/ECHA guidance document for the ED assessment of a non-pesticide chemical regulated under REACH. A data dossier was built by a systematic literature search (Web of Science, Pubmed, Embase; n = 511), title/abstract screening (n = 124) and full text examination (n = 88). All the information was extracted and systematically reported for 309 parameters (100 for adversity; 209 for endocrine activity). The reliability of studies was assessed (SciRAP tool). RESULTS: Data were synthesized into 96 lines of evidence for adversity (n = 57), and endocrine activity (n = 39); and assessed by weight of evidence methodology. The initial analysis of the evidence indicated EATS-mediated adversity in mammals, therefore a mode of action (MoA) was postulated for both male and female adult exposure. Female MoA included estrogen receptor activation and altered steroidogenesis leading to ovarian dysfunction, altered estrous cycling and impaired female fertility. Male MoA was initiated by androgen receptor inhibition and altered steroidogenesis leading to dysfunction of male reproductive organs and impaired male fertility. CONCLUSIONS: The overall conclusion of the ED assessment indicated that BPAF meets the ED criteria for human health. The steps described in the ED guidance document were successfully completed, resulting in a thorough, structured and transparent identification of BPAF as an ED. Advantages and limitations of applying the ED criteria and guidance for a REACH chemical are discussed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12940-021-00731-0. BioMed Central 2021-04-24 /pmc/articles/PMC8070297/ /pubmed/33894771 http://dx.doi.org/10.1186/s12940-021-00731-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Escrivá, Laura Zilliacus, Johanna Hessel, Ellen Beronius, Anna Assessment of the endocrine disrupting properties of bisphenol AF: a case study applying the European regulatory criteria and guidance |
title | Assessment of the endocrine disrupting properties of bisphenol AF: a case study applying the European regulatory criteria and guidance |
title_full | Assessment of the endocrine disrupting properties of bisphenol AF: a case study applying the European regulatory criteria and guidance |
title_fullStr | Assessment of the endocrine disrupting properties of bisphenol AF: a case study applying the European regulatory criteria and guidance |
title_full_unstemmed | Assessment of the endocrine disrupting properties of bisphenol AF: a case study applying the European regulatory criteria and guidance |
title_short | Assessment of the endocrine disrupting properties of bisphenol AF: a case study applying the European regulatory criteria and guidance |
title_sort | assessment of the endocrine disrupting properties of bisphenol af: a case study applying the european regulatory criteria and guidance |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070297/ https://www.ncbi.nlm.nih.gov/pubmed/33894771 http://dx.doi.org/10.1186/s12940-021-00731-0 |
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