Evidence map›Paper›PMID 29427786›Full record

ArticleToxicology2018

CLARITY-BPA: Effects of chronic bisphenol A exposure on the immune system: Part 2 - Characterization of lymphoproliferative and immune effector responses by splenic leukocytes.

Jinpeng Li, Anthony Bach, Robert B Crawford, Ashwini S Phadnis-Moghe, Weimin Chen, Shawna D'Ingillo, Natalia Kovalova, Jose E Suarez-Martinez, Jiajun Zhou, Barbara L F Kaplan and 1 more

Open access · greenAbstract read
In one paragraph

Article in Toxicology, 2018. 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
2.6field-weighted citation impact, top 12% 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, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Bibliometric Analysis of the Toxicity of Bisphenol A.International journal of environmental research and public health · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Long-term Immunotoxic Effects of Oral Prenatal and Neonatal Atrazine Exposure.Toxicological sciences : an official journal of the Society of Toxicology · 2019
    Article
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

11 authors at 1 institution in 1 country.

Jinpeng LiInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Anthony BachInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Robert B CrawfordInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Ashwini S Phadnis-MogheInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Weimin ChenInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Shawna D'IngilloInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Natalia KovalovaInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Jose E Suarez-MartinezInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Jiajun ZhouInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Barbara L F KaplanInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States.
Norbert E KaminskiInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, United States; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, 48824, United States. Electronic address: kamins11@msu.edu.
Michigan State University · US

Funding

Integrative Training in the Pharmacological SciencesT32GM092715 · NIGMS · MICHIGAN STATE UNIVERSITY · PI NEUBIG, RICHARD R · 2011 to 2020
$1.5M
Immunotoxicology of Chronic Exposure to Estrogenic Bisphenol-AU01ES020885 · NIEHS · MICHIGAN STATE UNIVERSITY · PI KAMINSKI, NORBERT E · 2011 to 2014
$778k
NIEHS NIH HHS U01 ES020885NIGMS NIH HHS T32 GM092715
6 · The paper itself

Abstract

Bisphenol A (BPA) is commonly used in the manufacturing of a wide range of consumer products, including polycarbonate plastics, epoxy resin that lines beverage and food cans, and some dental sealants. Consumption of food and beverages containing BPA represents the primary route of human BPA exposure, which is virtually ubiquitous. An increasing number of studies have evaluated the effects of BPA on immune responses in laboratory animals that have reported a variety of effects some of which have been contradictory. To address the divergent findings surrounding BPA exposure, a comprehensive chronic treatment study of BPA was conducted in Sprague-Dawley rats, termed the Consortium Linking Academic and Regulatory Insights on Toxicity of BPA (CLARITY-BPA). As a participant in the CLARITY-BPA project, our studies evaluated the effects of BPA on a broad range of immune function endpoints using spleen cells isolated from BPA or vehicle treated rats. This comprehensive assessment included measurements of lymphoproliferation in response to mitogenic stimuli, immunoglobulin production by B cells, and cellular activation of T cells, NK cells, monocytes, granulocytes, macrophages and dendritic cells. In total, 630 different measurements in BPA treated rats were performed of which 35 measurements were statistically different from vehicle controls. The most substantive alteration associated with BPA treatment was the augmentation of lymphoproliferation in response to pokeweed mitogen stimulations in 1 year old male rats, which was also observed in the reference estrogen ethinyl estradiol treated groups. With the exception of the aforementioned, the statistically significant changes associated with BPA treatment were mostly sporadic and not dose-dependent with only one out of five BPA dose groups showing a statistical difference. In addition, the observed BPA-associated alterations were mostly moderate in magnitude and showed no persistent trend over the one-year time period. Based on these findings, we conclude that the observed BPA-mediated changes observed in this study are unlikely to alter immune competence in adult rats.

Indexed as

AnimalsBenzhydryl CompoundsBisphenol A CompoundsB-LymphocytesCell ProliferationCells, CulturedEndocrine DisruptorsImmunoglobulin MKiller Cells, NaturalLeukocyte CountLeukocytesLymphocyte CountLymphocytesMaleMyeloid CellsPhenolsBenzhydryl Compoundsbisphenol ABisphenol A CompoundsEndocrine DisruptorsImmunoglobulin MPhenolsBisphenol ABPACLARITY-BPAImmune systemImmunotoxicity

Identifiers

PMID29427786
PMCPMC5845800
OpenAlexW2789446348

What OpenQuestion holds

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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.