Weight of the Evidence Evaluation of Low-Dose Reproductive and Developmental Effects of Bisphenol A

$61.20 plus tax (Refund Policy)

Buy Article:

Abstract:

A panel convened by the Harvard Center for Risk Analysis (HCRA) evaluated the weight of evidence for potential developmental and reproductive toxicity of bisphenol A (BPA, CASRN 80-05-7) in animals at doses well below the Lowest Observed Adverse Effect Level (LOAEL) of 50 mg/kg-day previously identified by the U.S. Environmental Protection Agency (US EPA) and even US EPA's reference dose (RfD) of 0.05 mg/kg-day. The effects are hypothesized to occur through an endocrine-modulating mode of action, specifically through estrogen receptors. The panel focused on potential male reproductive effects but also examined other endpoints possibly associated with hormone-like effects. The review considered studies published through April 2002. A formal deliberation framework focused on consistency, generalizability, and biological plausibility. The panel found no consistent affirmative evidence of low-dose BPA effects for any endpoint. Inconsistent responses across rodent species and strains made generalizability of low-dose BPA effects questionable. Lack of adverse effects in two multiple-generation reproductive and developmental studies casts doubt on suggestions of significant physiological or functional impairment. The panel was concerned about generalization of non-oral administration results to oral exposures. Differences in the pattern of BPA responses compared to estradiol or diethylstilbestrol (DES) cast doubt on estrogenicity as a low-dose mechanism of action for BPA. Finally, there is indirect evidence that humans may be lesssensitive to possible estrogenic effects from BPA exposure due to pharmacodynamic factors. The panel recommended replication of existing studies under carefully controlled conditions and further study of BPA's pharmacokinetics and pharmacodynamics. The study was funded by a grant from the American Plastics Council.

Keywords: bisphenol A; developmental toxicity; endocrine disruption; reproductive toxicity; weight of evidence

Document Type: Research Article

DOI: http://dx.doi.org/10.1080/10807030490513883

Affiliations: 1: Harvard Center for Risk Analysis Harvard School of Public Health, Boston, Massachussets, USA 2: Department of Anatomy University of California, San Francisco, California, USA 3: Quintiles, Inc. 4: ToxPath, Inc. 5: Gradient Corporation 6: Department of Pharmacology/Toxicology University of Arizona 7: Center for Research for Mothers and Children National Institute of Child Health and Human Development, Bethesda, Maryland, USA

Publication date: October 1, 2004

Related content

Share Content

Access Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content
Cookie Policy
X
Cookie Policy
ingentaconnect website makes use of cookies so as to keep track of data that you have filled in. I am Happy with this Find out more