Evidence map›Paper›PMID 31756437›Full record

ArticleReproductive toxicology (Elmsford, N.Y.)2020

Fetal bisphenol A and ethinylestradiol exposure alters male rat urogenital tract morphology at birth: Confirmation of prior low-dose findings in CLARITY-BPA.

Kristen S Uchtmann, Julia A Taylor, Barry G Timms, Richard W Stahlhut, Emily A Ricke, Mark R Ellersieck, Frederick S Vom Saal, William A Ricke

Open access · greenAbstract read
In one paragraph

Article in Reproductive toxicology (Elmsford, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Kristen S UchtmannDepartment of Urology, University of Wisconsin, Madison, WI 53705 USA; George M. O'Brien Center of Research Excellence, University of Wisconsin, Madison, WI 53705 USA.
Julia A TaylorDivision of Biological Sciences, University of Missouri, Columbia, MO 65211 USA.
Barry G TimmsDivision of Basic Biological Sciences, University of South Dakota, Vermillion, SD 57069 USA.
Richard W StahlhutDivision of Biological Sciences, University of Missouri, Columbia, MO 65211 USA.
Emily A RickeDepartment of Urology, University of Wisconsin, Madison, WI 53705 USA; George M. O'Brien Center of Research Excellence, University of Wisconsin, Madison, WI 53705 USA.
Mark R EllersieckDepartment of Statistics, University of Missouri, Columbia, MO 65211 USA.
Frederick S Vom SaalDivision of Biological Sciences, University of Missouri, Columbia, MO 65211 USA.
William A RickeDepartment of Urology, University of Wisconsin, Madison, WI 53705 USA; University of Wisconsin Carbone Cancer Center, University of Wisconsin, Madison, WI 53705 USA; Molecular & Environmental Toxicology Center, University of Wisconsin, Madison, WI 53705 USA; George M. O'Brien Center of Research Excellence, University of Wisconsin, Madison, WI 53705 USA. Electronic address: rickew@urology.wisc.edu.
University of Missouri · USUniversity of Wisconsin–Madison · USUniversity of South Dakota · USUniversity of Wisconsin Carbone Cancer Center · US

Funding

Role of Beta-Catenin in Urinary DysfunctionU54DK104310 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI RICKE, WILLIAM A · 2014 to 2023
$12.8M
BPA: Cellular and epigenetic effects on the urethraU01ES020952 · NIEHS · UNIVERSITY OF MISSOURI-COLUMBIA · PI VOM SAAL, FREDERICK S · 2011 to 2014
$750k
NIDDK NIH HHS U54 DK104310NIEHS NIH HHS U01 ES020952
6 · The paper itself

Abstract

Bisphenol A (BPA) is a contaminant in virtually all Americans. To examine BPA's adverse effects, the FDA-NCTR, NIEHS, and 14 groups of academic scientists formed a consortium: CLARITY-BPA. The purpose of our study was to investigate the effects of a wide range of doses of BPA on fetal development of the NCTR CD-SD male rat urogenital sinus (UGS). Pregnant rats were administered BPA or positive control ethinylestradiol (EE2) daily, via oral gavage, from gestational day 6 through parturition. Tissues were collected on postnatal day 1 and the UGS was analyzed using computer-assisted 3-D reconstruction. Importantly, only low doses of BPA, as well as EE2, significantly changed birth weight and UGS morphology, including an increased size of the colliculus and decreased size of the urethra, consistent with prior reported BPA and EE2 effects. Our findings provide further evidence that BPA mediates nonmonotonic developmental effects on the fetal urogenital sinus.

Indexed as

AnimalsBenzhydryl CompoundsBisphenol A CompoundsEndocrine DisruptorsEstrogensEthinyl EstradiolFemaleFetal DevelopmentFetusHumansMaleMaternal-Fetal ExchangePhenolsPregnancyRats, Sprague-DawleyUrogenital AbnormalitiesBenzhydryl Compoundsbisphenol ABisphenol A CompoundsEndocrine DisruptorsEstrogensEthinyl EstradiolPhenolsBisphenol-ACLARITY-BPAEndocrine disruptionRodentsUrogenital sinus

Identifiers

PMID31756437
PMCPMC7339120
OpenAlexW2989583975

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.