Evidence map›Paper›PMID 31926854›Full record

Trial reportJACC. Heart failure2020

Mineralocorticoid Receptor Antagonists, Blood Pressure, and Outcomes in Heart Failure With Reduced Ejection Fraction.

Matteo Serenelli, Alice Jackson, Pooja Dewan, Pardeep S Jhund, Mark C Petrie, Patrick Rossignol, Gianluca Campo, Bertram Pitt, Faiez Zannad, João Pedro Ferreira and 1 more

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JACC. Heart failure, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
6.4field-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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Observational
  4. Review
  5. Review
  6. Article
  7. Heart Failure with Preserved Ejection Fraction: Challenges and Current Approaches.Research in heart yield and translational medicine · 2026
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Adverse Effects of Aldosterone: Beyond Blood Pressure.Journal of the American Heart Association · 2024
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 4 countries.

Matteo SerenelliBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom; Cardiovascular Centre of Ferrara University, Ferrara University, Ferrara, Italy.
Alice JacksonBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.
Pooja DewanBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.
Pardeep S JhundBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.
Mark C PetrieBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.
Patrick RossignolCentre d'Investigations Cliniques Plurithématique 1433, Université de Lorraine INSERM, CHRU de Nancy, F-CRIN INI-CRCT, Nancy France.
Gianluca CampoCardiovascular Centre of Ferrara University, Ferrara University, Ferrara, Italy; Gruppo Villa Maria Care & Research, Maria Cecilia Hospital, Cotignola (RA), Italy.
Bertram PittDepartment of Internal Medicine-Cardiology, University of Michigan School of Medicine, Ann Arbor, Michigan.
Faiez ZannadCentre d'Investigations Cliniques Plurithématique 1433, Université de Lorraine INSERM, CHRU de Nancy, F-CRIN INI-CRCT, Nancy France.
João Pedro FerreiraBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom; Centre d'Investigations Cliniques Plurithématique 1433, Université de Lorraine INSERM, CHRU de Nancy, F-CRIN INI-CRCT, Nancy France.
John J V McMurrayBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom. Electronic address: john.mcmurray@glasgow.ac.uk.
British Heart Foundation · GBCentre d'Investigation Clinique Pierre Drouin · FRFrench Clinical Research Infrastructure Network · FRMaria Cecilia Hospital · ITMichigan Medicine · USUniversité de Lorraine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe purpose of this study was to investigate the effects of mineralocorticoid receptor antagonists (MRAs) on systolic blood pressure (SBP) and outcomes according to baseline SBP in patients with heart failure with reduced ejection fraction (HFrEF).

backgroundMRAs are greatly underused in patients with HFrEF, often because of fear of adverse events. Concern about hypotension has been raised by the demonstration that MRAs are particularly effective treatment for resistant hypertension.

methodsThe effect of MRA therapy was studied in 4,396 patients with HFrEF randomized in the RALES (Randomized Aldactone Evaluation Study) and EMPHASIS-HF (Eplerenone in Mild Patients Hospitalization and Survival Study in Heart Failure) trials.

resultsMean SBP change from baseline to 6 months was +1.4 ± 18.1 mm Hg in the placebo group and -1.2 ± 17.9 mm Hg in the MRA group. The between-treatment difference was 2.6 mm Hg (95% confidence interval [CI]: 1.5 to 3.6; p < 0.001). All outcomes were reduced by MRA therapy overall, with consistent effects across SBP categories (e.g., all-cause mortality, overall hazard ratio [HR] of 0.72; 95% CI: 0.64 to 0.82; p < 0.001; SBP ≤105 mm Hg; HR: 0.72; 95% CI: 0.56 to 0.94; SBP >105 to ≤115 mm Hg; HR: 0.78; 95% CI: 0.60 to 1.02; SBP >115 to ≤125 mm Hg; HR: 0.71; 95% CI: 0.53 to 0.94; SBP >125 to ≤135 mm Hg; HR: 0.79; 95% CI: 0.57 to 1.10; and SBP > 135 mm Hg; HR: 0.67; 95% CI: 0.50 to 0.90; p for interaction = 0.95). Hypotension was infrequent and not more common with MRA therapy than with placebo, overall (4.6% vs. 3.9%; p = 0.25) or in any SBP category.

conclusionsMRA treatment had little effect on SBP in patients with HFrEF, and the clinical benefits were not modified by baseline SBP. MRA treatment infrequently caused hypotension, even when the baseline SBP was low. The treatment discontinuation rates between MRA and placebo therapy were similar. Low SBP is not a reason to withhold MRA therapy in patients with HFrEF.

Indexed as

AgedBlood PressureEplerenoneFemaleHeart FailureHumansMaleMineralocorticoid Receptor AntagonistsSpironolactoneStroke VolumeTreatment OutcomeEplerenoneMineralocorticoid Receptor AntagonistsSpironolactonealdosteroneblood pressureejection fractioneplerenoneheart failuremineralocorticoid receptorspironolactone

Identifiers

PMID31926854
PMCPMC7086149
OpenAlexW2999355589

What OpenQuestion holds

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LicenceCC BY
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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.