Evidence map›Paper›PMID 34222720›Full record

ArticleJACC. Basic to translational science2021

STOP-HF Trial: Higher Endogenous BNP and Cardiovascular Protection in Subjects at Risk for Heart Failure.

Valentina Cannone, Mark Ledwidge, Chris Watson, Paul M McKie, John C Burnett, Kenneth McDonald

Open access · goldAbstract read
In one paragraph

Article in JACC. Basic to translational science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The Genetic Polymorphisms ofInternational journal of molecular sciences · 2025
    Article
  5. Sex-based differences in metabolic protection by the ANP genetic variant rs5068 in the general population.American journal of physiology. Heart and circulatory physiology · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. BNP and Precision Medicine: Tip of an Iceberg.JACC. Basic to translational science · 2021
    Article
  11. 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

6 authors at 3 institutions in 4 countries.

Valentina CannoneCardiorenal Research Laboratory, Division of Circulatory Failure, Department of Cardiovascular Disease, Mayo Clinic, Rochester, Minnesota, USA.
Mark LedwidgeSTOP-HF Unit, St Vincent's University Healthcare Group, Dublin, Ireland.
Chris WatsonUCD Conway Institute, School of Medicine, University College Dublin, Dublin, Ireland.
Paul M McKieCardiorenal Research Laboratory, Division of Circulatory Failure, Department of Cardiovascular Disease, Mayo Clinic, Rochester, Minnesota, USA.
John C BurnettCardiorenal Research Laboratory, Division of Circulatory Failure, Department of Cardiovascular Disease, Mayo Clinic, Rochester, Minnesota, USA.
Kenneth McDonaldSTOP-HF Unit, St Vincent's University Healthcare Group, Dublin, Ireland.
University College Dublin · IEMayo Clinic · USUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B-type natriuretic peptide (BNP) possesses blood-pressure-lowering, antifibrotic, and aldosterone-suppressing properties. In Stage A and B heart failure, the carriers of the minor C allele of the BNP genetic variant rs198389 have higher circulating levels of BNP and are at decreased risk of hypertension, new-onset left ventricular systolic dysfunction, and hospitalization for major adverse cardiovascular events. Future studies are warranted to investigate the role of BNP genetic testing and BNP-based therapy in the prevention of heart failure.

Indexed as

BNP, B-type natriuretic peptideB-type natriuretic peptideheart failureHF, heart failureLVSD, left ventricular systolic dysfunctionpGC-A, particulate guanylyl cyclase A receptorRAAS, renin-angiotensin-aldosterone systemrs198389single nucleotide polymorphismSNP, single nucleotide polymorphismSTOP-HF Trial

Identifiers

PMID34222720
PMCPMC8246026
OpenAlexW3168479654

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.