Evidence map›Paper›PMID 31485760›Full record

ReviewCurrent hypertension reports2019

Mineralocorticoid Receptor and Endothelial Dysfunction in Hypertension.

Jessica L Faulkner, Eric J Belin de Chantemèle

Open access · greenAbstract readReview
In one paragraph

Review in Current hypertension reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
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  9. Article
  10. Review
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  12. Is fluid retention a cardiovascular risk factor?Clinical hemorheology and microcirculation · 2024
    Review
  13. Review
  14. Sex differences in autonomic responses to stress: implications for cardiometabolic physiology.American journal of physiology. Endocrinology and metabolism · 2022
    Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  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

2 authors at 1 institution in 1 country.

Jessica L FaulknerVascular Biology Center, Department of Medicine (Cardiology), Medical College of Georgia, Augusta University, 1460 Laney Walker Blvd., Augusta, GA, 30912, USA.
Eric J Belin de ChantemèleVascular Biology Center, Department of Medicine (Cardiology), Medical College of Georgia, Augusta University, 1460 Laney Walker Blvd., Augusta, GA, 30912, USA. ebelindechanteme@augusta.edu.
Augusta University · US

Funding

Leptin in HIV associated vascular diseasesR01HL147639 · NHLBI · AUGUSTA UNIVERSITY · PI BELIN DE CHANTEMELE, ERIC J · 2020 to 2023
$2.0M
Aldosterone Contribution to Leptin-mediated Hypertension in Obese FemalesR01HL130301 · NHLBI · AUGUSTA UNIVERSITY · PI BELIN DE CHANTEMELE, ERIC J · 2016 to 2020
$1.9M
A novel role for endothelial mineralocorticoid receptors in obesity-associated cardiovascular disease in femalesK99HL146948 · NHLBI · AUGUSTA UNIVERSITY · PI FAULKNER, JESSICA L. · 2019 to 2020
$220k
Endothelial Mineralocorticoid Receptors: Novel Mechanism for Sex-Discrepancies in Vascular Disorders Associated with ObesityF32HL136191 · NHLBI · AUGUSTA UNIVERSITY · PI FAULKNER, JESSICA L. · 2017 to 2018
$111k
NHLBI NIH HHS F32 HL136191NHLBI NIH HHS K99 HL146948NHLBI NIH HHS R01 HL130301NHLBI NIH HHS R01 HL147639
6 · The paper itself

Abstract

purpose of reviewTo review the latest reports of the contributions of the endothelial mineralocorticoid receptor to endothelial dysfunction and hypertension to begin to determine the clinical potential for this pathway for hypertension treatment. RECENT

findingsEndothelial mineralocorticoid receptor expression is sex-specifically increased in female mice and humans compared with males. Moreover, the expression of endothelial mineralocorticoid receptors is increased by endothelial progesterone receptor activation and naturally occurring fluctuations in progesterone levels (estrous, pregnancy) predict endothelial mineralocorticoid receptor expression levels in female mice. These data follow many previous reports that have indicated that endothelial mineralocorticoid receptor deletion is protective in the development of obesity- and diabetes-associated endothelial dysfunction in female mouse models. These studies have more recently been followed up by reports indicating that both intact endothelial mineralocorticoid receptor and progesterone receptor expression are required for obesity-associated, leptin-mediated endothelial dysfunction in female mice. In addition, the intra-endothelial signaling pathway for endothelial mineralocorticoid receptors to induce dysfunction requires the intact expression of α-epithelial sodium channels (αENaC) in endothelial cells in females. Endothelial mineralocorticoid receptors are sex-specifically upregulated in the vasculature of females, a sex difference which is driven by endothelial progesterone receptor activation, and increased activity of these endothelial mineralocorticoid receptors is a crucial mediator of endothelial dysfunction, and potentially hypertension, in obese female experimental models.

Indexed as

AldosteroneAnimalsDisease Models, AnimalEndothelial CellsEndothelium, VascularEpithelial Sodium ChannelsFemaleHumansHypertensionLeptinMaleMiceMineralocorticoid Receptor AntagonistsObesityReceptors, MineralocorticoidReceptors, ProgesteroneAldosteroneEpithelial Sodium ChannelsLeptinMineralocorticoid Receptor AntagonistsReceptors, MineralocorticoidReceptors, ProgesteroneEndothelial dysfunctionEndothelial MRHypertensionObesityProgesteroneSex differences

Identifiers

PMID31485760
PMCPMC6878110
OpenAlexW2971498957

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.