Evidence map›Paper›PMID 39654426›Full record

ArticleEuropean journal of heart failure2025

Machine learning approach to identify phenotypes in patients with ischaemic heart failure with reduced ejection fraction.

Luca Monzo, Emmanuel Bresso, Kenneth Dickstein, Bertram Pitt, John G F Cleland, Stefan D Anker, Carolyn S P Lam, Mandeep R Mehra, Dirk J van Veldhuisen, Barry Greenberg and 2 more

Abstract read
In one paragraph

Article in European journal of heart failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

12 authors.

Luca MonzoUniversité de Lorraine, INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Inserm U1116, CHRU de Nancy and F-CRIN INI-CRCT, Nancy, France.ORCID https://orcid.org/0000-0003-2958-943X
Emmanuel BressoUniversité de Lorraine, INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Inserm U1116, CHRU de Nancy and F-CRIN INI-CRCT, Nancy, France.
Kenneth DicksteinDepartment of Cardiology, University of Bergan, Stavanger University Hospital, Stavanger, Norway.
Bertram PittDivision of Cardiology, Department of Medicine, University of Michigan, Ann Arbor, MI, USA.
John G F ClelandRobertson Centre for Biostatistics and Clinical Trials, University of Glasgow, Glasgow, UK.
Stefan D AnkerBerlin-Brandenburg Center for Regenerative Therapies, Berlin, Germany.
Carolyn S P LamNational Heart Centre Singapore, Duke-National University of Singapore, Singapore, Singapore.
Mandeep R MehraHeart and Vascular Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Dirk J van VeldhuisenDepartment of Cardiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Barry GreenbergCardiology Division, Department of Medicine, University of California San Diego, La Jolla, CA, USA.
Faiez Zannad *Université de Lorraine, INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Inserm U1116, CHRU de Nancy and F-CRIN INI-CRCT, Nancy, France.
Nicolas Girerd *Université de Lorraine, INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Inserm U1116, CHRU de Nancy and F-CRIN INI-CRCT, Nancy, France.

Funding

Contrat de Plan Etat Région LorraineFonds Européen de Développement Régional
6 · The paper itself

Abstract

aimsPatients experiencing ischaemic heart failure with reduced ejection fraction (HFrEF) represent a diverse group. We hypothesize that machine learning clustering can help separate distinctive patient phenotypes, paving the way for personalized management. METHODS AND

resultsA total of 8591 ischaemic HFrEF patients pooled from the EPHESUS and CAPRICORN trials (64 ± 12 years; 28% women) were included in this analysis. Clusters were identified using both clinical and biological variables. Association between clusters and the composite of (i) heart failure hospitalization or all-cause death, (ii) cardiovascular (CV) hospitalization or all-cause death, and (iii) major adverse CV events was assessed. The derived algorithm was applied in the COMMANDER-HF trial (n = 5022) for external validation. Five clinical distinctive clusters were identified: Cluster 1 (n = 2161) with the older patients, higher prevalence of atrial fibrillation and previous CV events; Cluster 2 (n = 1376) with the higher prevalence of older hypertensive women and smoking habit; Cluster 3 (n = 1157) with the higher prevalence of diabetes and peripheral artery disease; Cluster 4 (n = 2073) with relatively younger patients, mostly men and with the higher left ventricular ejection fraction; Cluster 5 (n = 1824) with the younger patients and lower CV events burden. Cluster membership was efficiently predicted by a random forest algorithm. Clusters were significantly associated with outcomes in derivation and validation datasets, with Cluster 1 having the highest risk, and Cluster 4 the lowest. Mineralocorticoid receptor antagonist benefit on CV hospitalization or all-cause death was magnified in clusters with the lowest risk of events (Clusters 2 and 4).

conclusionsClustering reveals distinct risk subgroups in the heterogeneous array of ischaemic HFrEF patients. This classification, accessible online, could enhance future outcome predictions for ischaemic HFrEF cases.

Indexed as

Heart FailureMachine LearningMyocardial IschemiaStroke VolumeVentricular Function, LeftAgedFemaleHospitalizationHumansMaleMiddle AgedPhenotypeClinical outcomesClusteringHFrEFIschaemic heart diseaseMachine learning

Identifiers

PMID39654426
PMCPMC12803694

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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.