Evidence map›Paper›PMID 30678859›Full record

ReviewVitamins and hormones2019

Leptin and Aldosterone.

Jessica L Faulkner, Eric J Belin de Chantemèle

Open access · greenAbstract readReview
In one paragraph

Review in Vitamins and hormones, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Unmasking Hormonal Mechanisms of Hypertension in Obesity.JACC. Basic to translational science · 2026
    Article
  4. Review
  5. Emerging Role of Leptin in Vascular and Placental Dysfunction in Preeclampsia.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Aldosterone breakthrough as a clue to the physiological importance of paracrine regulation of aldosterone secretion.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Article
  10. Article
  11. Review
  12. Review
  13. Chronic CNS-mediated cardiometabolic actions of leptin: potential role of sex differences.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  14. Review
  15. Review
  16. Review
  17. Review
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, Medical College of Georgia at Augusta University, Augusta, GA, United States.
Eric J Belin de ChantemèleVascular Biology Center, Medical College of Georgia at Augusta University, Augusta, GA, United States. Electronic address: ebelindechanteme@augusta.edu.
Augusta University · US

Funding

Aldosterone Contribution to Leptin-mediated Hypertension in Obese FemalesR01HL130301 · NHLBI · AUGUSTA UNIVERSITY · PI BELIN DE CHANTEMELE, ERIC J · 2016 to 2020
$1.9M
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 R01 HL130301
6 · The paper itself

Abstract

The prominence of obesity in the clinical population as well as the strong association of cardiovascular risk factors with obesity has prompted the investigation of the adipose tissue and its physiological contribution to cardiovascular health. A notable finding in these investigations was the discovery of the adipocyte-derived hormone leptin. Leptin is secreted from the adipose tissue, increases in linear fashion in the circulation with increased body mass and is implicated in the development of cardiovascular disease in obesity, notably via pro-hypertensive mechanisms. Leptin stimulates the activation of the sympathetic nervous system in male patients and mice, which has been implicated as the pro-hypertensive pathway for leptin in obesity. However, obese premenopausal females do not exhibit increased sympathetic activation in response to hyperleptinemia in obesity, indicating a sex-discrepancy in mechanisms of obesity-associated hypertension. Our lab recently demonstrated that leptin also induces the adrenal production of aldosterone in a direct fashion and that this pathway leads to the hyperaldosteronemia that is characteristic of obesity. We have also published data that indicate that the implications of leptin-induced aldosterone are of particular impact in obese females. Leptin-mediated hypertension and endothelial dysfunction, a significant predictor of hypertension clinically, require activation of the mineralocorticoid receptor in female mice. The clinical potential of this pathway remains under investigation; however, existing data indicate that a sex discrepancy exists in mechanisms of leptin-mediated hypertension between males and females and that leptin-stimulated aldosterone plays a significant role in females.

Indexed as

AldosteroneAnimalsFemaleGene Expression RegulationHumansHypertensionLeptinMaleObesitySex FactorsAldosteroneLeptinAldosteroneEndothelial dysfunctionHypertensionLeptinMineralocorticoid receptorSex differences

Identifiers

PMID30678859
PMCPMC9631097
OpenAlexW2902085023

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.