Evidence map›Paper›PMID 39319458›Full record

ArticleHypertension (Dallas, Tex. : 1979)2024

ENaCγ in Urinary Extracellular Vesicles as an Indicator of MR Signaling in Primary Aldosteronism.

Yuto Hayama, Emiko Kuribayashi-Okuma, Norihiko Fujii, Fumika Ochiai-Homma, Osamu Yamazaki, Yuya Tsurutani, Tetsuo Nishikawa, Shigeru Shibata

Abstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. How potassium intake regulates sodium excretion in the kidney? Aldosterone-independent pathway in human.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    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

8 authors.

Yuto HayamaDivision of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan (Y.H., E.K.-O., F.O.-H., O.Y., S.S.).
Emiko Kuribayashi-OkumaDivision of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan (Y.H., E.K.-O., F.O.-H., O.Y., S.S.).
Norihiko FujiiRadioisotope Research Center (N.F.), Teikyo University, Japan.
Fumika Ochiai-HommaDivision of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan (Y.H., E.K.-O., F.O.-H., O.Y., S.S.).
Osamu YamazakiDivision of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan (Y.H., E.K.-O., F.O.-H., O.Y., S.S.).ORCID 0000-0002-4251-403X
Yuya TsurutaniEndocrionology and Diabetes Center, Yokohama Rosai Hospital, Japan (Y.T., T.N.).ORCID 0000-0001-5831-3286
Tetsuo NishikawaEndocrionology and Diabetes Center, Yokohama Rosai Hospital, Japan (Y.T., T.N.).ORCID 0000-0002-8271-7368
Shigeru ShibataDivision of Nephrology, Department of Internal Medicine, Teikyo University School of Medicine, Japan (Y.H., E.K.-O., F.O.-H., O.Y., S.S.).ORCID 0000-0002-6868-0626

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAldosterone and the MR (mineralocorticoid receptor) are important therapeutic targets for hypertension and cardiovascular diseases. However, biomarkers of tissue MR signaling are not fully established. Extracellular vesicles released from eukaryotic cells can provide information on tissue signaling. Using samples from patients with primary aldosteronism (PA), we explored the potential of urinary extracellular vesicles (uEVs) as a noninvasive indicator of MR signaling to guide treatment.

methodsWe analyzed proteins contained in PA uEVs by liquid chromatography tandem mass spectrometry. We narrowed down candidate biomarkers by referring to an existing database of urinary exosomes. The results were validated through Western blot analysis involving 63 patients with PA and 11 healthy volunteers.

resultsWe identified a total of 1940 proteins in PA uEVs. Comparative analysis with the existing database narrowed down the pathways enriched in PA uEVs, which were related to diabetic complications, Rac1 signaling, and aldosterone-regulated sodium reabsorption. A closer look at the identified proteins revealed ENaCγ (epithelial Na

conclusionsThis study provides a list of proteins contained in PA uEVs and suggests that ENaCγ in uEVs is a promising biomarker for renal MR signaling.

Indexed as

AldosteroneBiomarkersEpithelial Sodium ChannelsExtracellular VesiclesHyperaldosteronismReceptors, MineralocorticoidSignal TransductionAdultChromatography, LiquidFemaleHumansMaleMiddle AgedTandem Mass SpectrometryAldosteroneBiomarkersEpithelial Sodium ChannelsReceptors, MineralocorticoidSCNN1G protein, humanbiomarkerseukaryotic cellsexosomeshormonespeptidesreceptors, cytoplasmic and nuclearsodium

Identifiers

PMID39319458
PMCPMC11578056

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Registered trials

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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.