Evidence map›Paper›PMID 41356890›Full record

ArticleCureus2025

The Role of Myocardial Fibrosis and Bioenergetic Dysfunction in Heart Failure Prognosis: A Study Protocol.

Mário Barbosa, Ana Melicio, Ana Matias, Mafalda Santos, João M Lopes, Laura Aguiar, Joana Ferreira, Ângela Inácio, Manuel Bicho, Luiz M Falcão

Abstract read
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Mário BarbosaDepartment of Internal Medicine, Hospital Lusíadas Lisboa, Lisbon, PRT.
Ana MelicioDepartment of Internal Medicine, Santa Maria Local Health Unit, Lisbon, PRT.
Ana MatiasGenetics Laboratory, Faculty of Medicine of the University of Lisbon, Lisbon, PRT.
Mafalda SantosGenetics Laboratory, Faculty of Medicine of the University of Lisbon, Lisbon, PRT.
João M LopesDepartment of Internal Medicine, Santa Maria Local Health Unit, Lisbon, PRT.
Laura AguiarInstitute of Environmental Health, Associated Earth Laboratory, Faculty of Medicine of the University of Lisbon, Lisbon, PRT.
Joana FerreiraInstitute of Environmental Health, Associated Earth Laboratory, Faculty of Medicine of the University of Lisbon, Lisbon, PRT.
Ângela InácioGenetics Laboratory, Faculty of Medicine of the University of Lisbon, Lisbon, PRT.
Manuel BichoGenetics Laboratory, Faculty of Medicine of the University of Lisbon, Lisbon, PRT.
Luiz M FalcãoDepartment of Genetics, Bento da Rocha Cabral Scientific Research Institute, Lisbon, PRT.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction The blockage of the renin-angiotensin-aldosterone and sympathetic nervous systems is fundamental in heart failure (HF) treatment; nonetheless, other mechanisms related to myocardial fibrosis and bioenergetic dysfunction also have a relevant role in the genesis and progression of this syndrome. We aim to stratify the short-term outcome of patients hospitalized with acute decompensated heart failure (ADHF) in New York Heart Association (NYHA) class III or IV based on myocardial fibrosis biomarkers galectin-3 (Gal-3), suppression of tumorigenicity 2 (ST2) and growth differentiation factor15 (GDF-15), and bioenergetic dysfunction markers (absolute iron deficiency and functional iron deficiency). Secondary endpoints were evaluation of short-term prognosis through early HF readmission and all-cause mortality (up to 90 days after hospital discharge), annual heart failure readmission and all-cause mortality, and annual risk for major adverse cardiovascular events (MACE), namely fatal and non-fatal stroke and fatal and non-fatal myocardial infarction, and cardiorenal syndrome.  Material and methods This cohort prospective observational unicentric study had two arms (left ventricular ejection fraction (LVEF)> 40% and ≤ 40%). A total of 128 participants were included, with 64 per group. Gal-3, ST2, and GDF-15 will be assessed in vitroin serum and plasma, and iron kinetics will be evaluated in plasma. Kaplan-Meier survival estimates will be calculated for each endpoint. A univariate Cox propor-tional hazards model will be performed to achieve hazard ratios and 95% confidence intervals for each variable. Results We expect to establish a relation between high values of fibrosis biomarkers, absolute and functional iron deficiency, and impaired short-term outcome in patients admitted due to ADHF. Conclusions This study may yield knowledge regarding the role of myocardial fibrosis and bioenergetic dysfunction in HF short-term prognosis.

Indexed as

bioenergetic dysfunctiongalectin-3gdf-15heart failurest2

Identifiers

PMID41356890
PMCPMC12680110

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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.