Evidence map›Paper›PMID 32114652›Full record

ReviewCurrent hypertension reports2020

Estrogen and Bisphenol A in Hypertension.

Zena Wehbe, Suzanne A Nasser, Ahmed El-Yazbi, Salam Nasreddine, Ali H Eid

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current hypertension reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
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  7. Article
  8. The pharmaco-epigenetics of hypertension: a focus on microRNA.Molecular and cellular biochemistry · 2024
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
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  19. Estrogen normalizes maternal HFD-induced vascular dysfunction in offspring by regulating ATR.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Article
  20. 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

5 authors at 4 institutions in 2 countries.

Zena WehbeDepartment of Biology, American University of Beirut, Beirut, Lebanon.
Suzanne A NasserDepartment of Pharmacology and Therapeutics, Beirut Arab University, Beirut, Lebanon.
Ahmed El-YazbiDepartment of Pharmacology and Toxicology, Faculty of Medicine, American University of Beirut, Bliss Street, Riad El Solh, PO Box 11-0236, Beirut, 1107-2020, Lebanon.
Salam NasreddineBiology Department, Faculty of Sciences-Section I, Groupe Anti-cancer therapeutic approaches (ATAC), Laboratory Rammal Rammal, Lebanese University, Beirut, Lebanon.
Ali H EidDepartment of Pharmacology and Toxicology, Faculty of Medicine, American University of Beirut, Bliss Street, Riad El Solh, PO Box 11-0236, Beirut, 1107-2020, Lebanon. ae81@aub.edu.lb.
American University of Beirut · LBAlexandria University · EGBeirut Arab University · LBLebanese University · LB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewCardiovascular disease (CVD) is a non-subsiding disease that remains a leading cause of morbidity and mortality. CVD has been associated with endocrine disruptors, such as bisphenol A (BPA). This review critically summarizes existing findings on BPA and hypertension, with particular attention to genomic, non-genomic, molecular, and cellular mechanisms of action that render BPA as a cardiovascular estrogenic disruptor. RECENT

findingsOwing to its similar estrogenic structure, BPA has been shown to affect various phenotypes that are regulated by the natural hormone, estrogen. Indeed, BPA has been shown to interact with estrogen receptors, located both in the cell membrane and in the cytoplasm/nucleus. Given that estrogen plays an important role in cardiovascular physiology, a contributing role for BPA in CVD would not be unexpected. Existing literature, though limited, established BPA as a source of disruption in cardiovascular health, particularly hypertension. However, effects of BPA are largely dependent on the dose, patient gender, tissue, and developmental stage of the exposed tissue/organ. Accumulating evidence argues for an adverse effect of BPA on blood pressure, with this effect being gender, dose, and time specific. Thus, comprehensive studies which take these factors and other parameters, like epigenetic factors, into account are warranted before a thorough understanding is at hand.

Indexed as

Benzhydryl CompoundsEstrogensHypertensionPhenolsBisphenol A CompoundsHumansBenzhydryl Compoundsbisphenol ABisphenol A CompoundsEstrogensPhenolsBisphenol ACardiovascular diseaseEnvironmental pollutionEstrogenHypertensionToxicology

Identifiers

PMID32114652
OpenAlexW3007332788

What Socratic 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 Socratic graph.