Evidence map›Paper›PMID 36219773›Full record

ArticleEuropean heart journal2022

Aldosterone in chronic kidney disease and renal outcomes.

Ashish Verma, Anand Vaidya, Sonu Subudhi, Sushrut S Waikar

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in European heart journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 101 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Renalase stimulates aldosterone production via PMCA4b/cAMP in NCI-H295R cells.Journal of enzyme inhibition and medicinal chemistry · 2026
    Article
  5. Article
  6. Salt and chronic kidney disease.Nature reviews. Nephrology · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Primary aldosteronism.Nature reviews. Disease primers · 2026
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Mineralocorticoid Receptor Antagonists in Dialysis.American journal of nephrology · 2026
    Review
  17. Review
  18. Article
  19. Diabetic kidney disease, biomarkers, and finerenone.Diabetes, obesity & metabolism · 2026
    Review
  20. Review

2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Ashish VermaSection of Nephrology, Department of Medicine, Boston University School of Medicine and Boston Medical Center, Renal Section, Evans Biomedical Research Center, 650 Albany Street, X504, Boston, MA 02118, USA.ORCID 0000-0001-9497-6327
Anand VaidyaCenter for Adrenal Disorders, Division of Endocrinology, Diabetes, and Hypertension, Brigham and Women's Hospital, Boston, MA 02115, USA.ORCID 0000-0002-0314-9252
Sonu SubudhiDepartment of Radiation Oncology, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID 0000-0002-5937-1880
Sushrut S WaikarSection of Nephrology, Department of Medicine, Boston University School of Medicine and Boston Medical Center, Renal Section, Evans Biomedical Research Center, 650 Albany Street, X504, Boston, MA 02118, USA.ORCID 0000-0003-4004-326X
Boston University · USBrigham and Women's Hospital · USMassachusetts General Hospital · US

Funding

Unrecognized Primary Aldosteronism as a Pathogenic Mechanism for Chronic Kidney Disease in DiabetesR01DK115392 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI Anand Vaidya · 2018 to 2026
$6.0M
The Role of G Proteins in Insulin ActionR01DK061618 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SALTIEL, ALAN R. · 2002 to 2016
$5.1M
Aldosterone, the Mineralocorticoid Receptor, and Cardiovascular Disease in ObesityR01HL153004 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI VAIDYA, ANAND · 2020 to 2024
$4.4M
Primary Aldosteronism Subtypes: Pathophysiology and Steroid SignaturesR01HL155834 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TURCU, ADINA F · 2021 to 2025
$3.5M
Harvard Chronic Kidney Disease Research Biopsy CenterUH3DK114915 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI ROSAS, SYLVIA E, WAIKAR, SUSHRUT S. · 2019 to 2021
$900k
The Boston University Kidney and Medical Engineering Program (BU-KIDMEP)R25DK128858 · NIDDK · BOSTON MEDICAL CENTER · PI CHITALIA, VIPUL C, WAIKAR, SUSHRUT S. · 2021 to 2025
$637k
Metabolomics and Renal Functional ReserveR21DK119751 · NIDDK · BOSTON MEDICAL CENTER · PI WAIKAR, SUSHRUT S. · 2019 to 2020
$503k
NHLBI NIH HHS R01 HL153004NHLBI NIH HHS R01 HL155834NIDDK NIH HHS R01 DK061618NIDDK NIH HHS R01 DK115392NIDDK NIH HHS R21 DK119751NIDDK NIH HHS R25 DK128858NIDDK NIH HHS UH3 DK114915
6 · The paper itself

Abstract

aimsRandomized controlled trials have demonstrated the efficacy of mineralocorticoid receptor (MR) antagonism in delaying chronic kidney disease (CKD) progression in diabetes; however, they have not investigated the role of aldosterone or whether these beneficial effects could be achieved in individuals without diabetes. METHODS AND

resultsThe association between serum aldosterone concentrations and kidney disease progression was investigated among 3680 participants in the Chronic Renal Insufficiency Cohort. The primary outcome was CKD progression [defined as the composite of 50% decline in estimated glomerular filtration rate (eGFR) or end-stage kidney disease, whichever occurred first]. The associations between serum aldosterone and kidney disease outcomes were assessed using Cox proportional hazard models. At baseline, higher aldosterone concentrations were associated with a lower eGFR, lower serum potassium, greater urinary potassium, and protein excretion. Over a median follow-up of 9.6 years, 1412 participants developed CKD progression. In adjusted models, each doubling of serum aldosterone was associated with a 11% increased risk of CKD progression [hazard ratio (HR) 1.11, 95% confidence interval (CI) 1.04-1.18]. Individuals with the highest quartile of serum aldosterone had a 45% increased risk of CKD progression (HR 1.45, 95% CI 1.22-1.73) compared with the lowest quartile. The risk for CKD progression was similar regardless of whether patients had concomitant diabetes (P-interaction = 0.10).

conclusionHigher serum aldosterone levels among individuals with CKD are independently associated with an increased risk for kidney disease progression, irrespective of concomitant diabetes. These findings provide mechanistic support for MR antagonists in delaying CKD progression and suggest that they may also have a role in those without diabetes.

Indexed as

Diabetes MellitusRenal Insufficiency, ChronicAldosteroneDisease ProgressionGlomerular Filtration RateHumansKidneyMineralocorticoid Receptor AntagonistsPotassiumReceptors, MineralocorticoidRisk FactorsAldosteroneMineralocorticoid Receptor AntagonistsPotassiumReceptors, MineralocorticoidAldosteroneChronic kidney diseaseCRICDiabetesEnd-stage kidney disease

Identifiers

PMID36219773
PMCPMC10147385
OpenAlexW4304757244

What OpenQuestion holds

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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.