Evidence map›Paper›PMID 32438830›Full record

ArticleEnvironmental health perspectives2020

A Combined Morphometric and Statistical Approach to Assess Nonmonotonicity in the Developing Mammary Gland of Rats in the CLARITY-BPA Study.

Maël Montévil, Nicole Acevedo, Cheryl M Schaeberle, Manushree Bharadwaj, Suzanne E Fenton, Ana M Soto

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 41 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

6 authors at 2 institutions in 2 countries.

Maël MontévilDepartment of Integrative Physiology and Pathobiology, Tufts University School of Medicine, Boston Massachusetts, USA.
Nicole AcevedoDepartment of Integrative Physiology and Pathobiology, Tufts University School of Medicine, Boston Massachusetts, USA.
Cheryl M SchaeberleDepartment of Integrative Physiology and Pathobiology, Tufts University School of Medicine, Boston Massachusetts, USA.
Manushree BharadwajNational Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina, USA.
Suzanne E FentonNational Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina, USA.
Ana M SotoDepartment of Integrative Physiology and Pathobiology, Tufts University School of Medicine, Boston Massachusetts, USA.
Tufts University · USNational Institutes of Health · US

Funding

BPA as a Developmental CarcinogenU01ES020888 · NIEHS · TUFTS UNIVERSITY BOSTON · PI SOTO, ANA · 2011 to 2014
$909k
NIEHS NIH HHS U01 ES020888
6 · The paper itself

Abstract

backgroundThe Consortium Linking Academic and Regulatory Insights on Bisphenol-A (CLARITY-BPA) is a rare collaboration of guideline-compliant (core) studies and academic hypothesis-based studies to assess the effects of bisphenol A (BPA).

objectivesWe aimed to

methodsSprague-Dawley rats were exposed to BPA, vehicle, or positive control [ethinyl estradiol (EE2)] by oral gavage beginning on gestational day (GD)6 and continuing with direct dosing of the pups after birth. There were two studies: subchronic and chronic. The latter used two exposure regimes, one stopping at postnatal day (PND)21 (stop-dose) the other continuing until tissue harvest (continuous). Glands were harvested at multiple time points; whole mounts and histological specimens were analyzed blinded to treatment.

resultsThe subchronic study's semiquantitative analysis revealed no significant differences between control and BPA dose groups at PND21, whereas at PND90 there were significant differences between control and the lowest BPA dose and between control and the lowest EE2 dose in animals in estrus. Quantitative, automatized analysis of the chronic PND21 specimens displayed nonmonotonic BPA effects, with a breaking point between the 25 and

conclusionsBoth the semiquantitative and the quantitative methods revealed nonmonotonic effects of BPA. The quantitative unsupervised analysis used

Indexed as

AnimalsBenzhydryl CompoundsBisphenol A CompoundsEthinyl EstradiolFemaleHazardous SubstancesMammary Glands, AnimalPhenolsPregnancyRatsRats, Sprague-DawleyBenzhydryl Compoundsbisphenol ABisphenol A CompoundsEthinyl EstradiolHazardous SubstancesPhenols

Identifiers

PMID32438830
PMCPMC7263454
OpenAlexW3027149273

What OpenQuestion holds

Textmetadata
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.