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Implementation of the evidence‐based risk assessment for the re‐evaluation of Bisphenol A: preparatory work on cross‐sectional studies.

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Disclaimer: The present document has been produced and adopted by the bodies identified above as author. This task has been carried out exclusively by the author in the context of a contract between the European Food Safety Authority and the author, awarded following a tender procedure. The present document is published complying with the transparency principle to which the Authority is subject. It may not be considered as an output adopted by the Authority. The European Food Safety Authority reserves its rights, view and position as regards the issues addressed and the conclusions reached in the present document, without prejudice to the rights of the author.

Abstract

EFSA is implementing evidence‐based risk assessments for the re‐evaluation of the safety of bisphenol A (BPA) for human health. The aim of this work was to carry out some preparatory work for the working group on BPA re‐evaluation, with particular reference to the preparation of individual summary tables of human studies with cross‐sectional design, and a narrative and factual summary of the above studies when grouped by health outcome category and by effect/endpoint. The first stage of the work was conducted using DistillerSR, the web‐based systematic review software used by EFSA which enabled direct access/download to the published documents and provided an on‐line template for data extraction and reporting. A total of 161 published articles were considered and data extracted from these into the online templates. Using these data, with additional reference back to the published articles, a narrative report was produced that sub‐divided the studies into seven key toxicological areas: reproduction, neurotoxicity, immune system toxicity, metabolic effects, cardiovascular effects, carcinogenicity and general toxicity.