Literature DB >> 25304273

Evidence that bisphenol A (BPA) can be accurately measured without contamination in human serum and urine, and that BPA causes numerous hazards from multiple routes of exposure.

Frederick S vom Saal1, Wade V Welshons2.   

Abstract

There is extensive evidence that bisphenol A (BPA) is related to a wide range of adverse health effects based on both human and experimental animal studies. However, a number of regulatory agencies have ignored all hazard findings. Reports of high levels of unconjugated (bioactive) serum BPA in dozens of human biomonitoring studies have also been rejected based on the prediction that the findings are due to assay contamination and that virtually all ingested BPA is rapidly converted to inactive metabolites. NIH and industry-sponsored round robin studies have demonstrated that serum BPA can be accurately assayed without contamination, while the FDA lab has acknowledged uncontrolled assay contamination. In reviewing the published BPA biomonitoring data, we find that assay contamination is, in fact, well controlled in most labs, and cannot be used as the basis for discounting evidence that significant and virtually continuous exposure to BPA must be occurring from multiple sources.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Biomonitoring; Bisphenol A; Contamination; Endocrine disrupting chemicals; Pharmacokinetics

Mesh:

Substances:

Year:  2014        PMID: 25304273      PMCID: PMC4805123          DOI: 10.1016/j.mce.2014.09.028

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  103 in total

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4.  Sensitive method for the determination of bisphenol-A in serum using two systems of high-performance liquid chromatography.

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Review 6.  Human exposure to bisphenol A (BPA).

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Review 9.  Large effects from small exposures. I. Mechanisms for endocrine-disrupting chemicals with estrogenic activity.

Authors:  Wade V Welshons; Kristina A Thayer; Barbara M Judy; Julia A Taylor; Edward M Curran; Frederick S vom Saal
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10.  Relative binding affinity-serum modified access (RBA-SMA) assay predicts the relative in vivo bioactivity of the xenoestrogens bisphenol A and octylphenol.

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Review 6.  Bisphenol A exposure pathways in early childhood: Reviewing the need for improved risk assessment models.

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7.  In utero bisphenol A concentration, metabolism, and global DNA methylation across matched placenta, kidney, and liver in the human fetus.

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