Evidence mapPaperPMID 37610001Full record

ReviewJournal of molecular endocrinology2023

Vascular endothelial mineralocorticoid receptors and epithelial sodium channels in metabolic syndrome and related cardiovascular disease.

Guanghong Jia, Michael A Hill, James R Sowers

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of molecular endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Observational
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Emerging Role of Leptin in Vascular and Placental Dysfunction in Preeclampsia.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  13. miR-92a aggravates metabolic syndrome via KLF2/miR-483 axis.Journal of diabetes investigation · 2025
    Article
  14. Review
  15. Review
  16. The mineralocorticoid receptor in diabetic kidney disease.American journal of physiology. Renal physiology · 2024
    Review
  17. Review
  18. Diabetic Vasculopathy: Molecular Mechanisms and Clinical Insights.International journal of molecular sciences · 2024
    Review
  19. Impact ofFrontiers in gastroenterology (Lausanne, Switzerland) · 2024
    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

3 authors at 1 institution in 1 country.

Guanghong JiaDepartment of Medicine-Endocrinology and Metabolism, University of Missouri School of Medicine, Columbia, Missouri, USA.ORCID 0000-0003-0018-5925
Michael A HillDalton Cardiovascular Research Center, University of Missouri, Columbia, Missouri, USA.
James R SowersDepartment of Medicine-Endocrinology and Metabolism, University of Missouri School of Medicine, Columbia, Missouri, USA.
University of Missouri · US

Funding

Endothelial mineralocorticoid receptors in diet-induced skeletal muscle insulin resistanceR01DK124329 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · 2022 to 2025
$1.5M
ANG II OPPOSES INS MEDIATED VASORELAXATION &GLU UTILZAR01HL073101 · UNIVERSITY OF MISSOURI-COLUMBIA · 2004 to 2005
$586k
NHLBI NIH HHS R01 HL073101NHLBI NIH HHS R01 HL085119NHLBI NIH HHS R01 HL107910NIDDK NIH HHS R01 DK124329
6 · The paper itself

Abstract

Metabolic syndrome is a group of risk factors that increase the risk of developing metabolic and cardiovascular disease (CVD) and include obesity, dyslipidemia, insulin resistance, atherosclerosis, hypertension, coronary artery disease, and heart failure. Recent research indicates that excessive production of aldosterone and associated activation of mineralocorticoid receptors (MR) impair insulin metabolic signaling, promote insulin resistance, and increase the risk of developing metabolic syndrome and CVD. Moreover, activation of specific epithelial sodium channels (ENaC) in endothelial cells (EnNaC), which are downstream targets of endothelial-specific MR (ECMR) signaling, are also believed to play a crucial role in the development of metabolic syndrome and CVD. These adverse effects of ECMR/EnNaC activation are mediated by increased oxidative stress, inflammation, and lipid metabolic disorders. It is worth noting that ECMR/EnNaC activation and the pathophysiology underlying metabolic syndrome and CVD appears to exhibit sexual dimorphism. Targeting ECMR/EnNaC signaling may have a beneficial effect in preventing insulin resistance, diabetes, metabolic syndrome, and related CVD. This review aims to examine our current understanding of the relationship between MR activation and increased metabolic syndrome and CVD, with particular emphasis placed on the role for endothelial-specific ECMR/EnNaC signaling in these pathological processes.

Indexed as

Cardiovascular DiseasesInsulin ResistanceMetabolic SyndromeEndothelial CellsEpithelial Sodium ChannelsHumansReceptors, MineralocorticoidEpithelial Sodium ChannelsReceptors, Mineralocorticoidendothelial cellsepithelial sodium channelsmetabolic syndromemineralocorticoid receptors

Identifiers

PMID37610001
PMCPMC10502958
OpenAlexW4386084825

What Socratic holds

Textmetadata
LicenceCC BY
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.