Evidence map›Paper›PMID 41058565›Full record

ArticleCirculation. Heart failure2026

Phenomapping in Heart Failure With Reduced Ejection Fraction to Identify Subpopulations With High Residual Risk: A VICTORIA Substudy.

Palak Shah, Yinggan Zheng, Burkert Pieske, Vojtech Melenovsky, Carolyn S P Lam, Karen Sliwa, Javed Butler, Justin A Ezekowitz, Christopher R deFilippi, Christopher M O'Connor and 7 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Circulation. Heart failure, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02861534 (A Randomized Parallel-Group, Placebo-Controlled, Double-Blind, Event-Driven, Multi-Center Pivotal Phase III Clinical Outcome Trial of Efficacy and Safety of the Oral sGC Stimulator Vericiguat in Subjects With Heart Failure With Reduced Ejection Fraction), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT02861534 phase3completednot on this map

A Randomized Parallel-Group, Placebo-Controlled, Double-Blind, Event-Driven, Multi-Center Pivotal Phase III Clinical Outcome Trial of Efficacy and Safety of the Oral sGC Stimulator Vericiguat in Subjects With Heart Failure With Reduced Ejection Fraction (HFrEF) - VerICiguaT GlObal Study in Subjects With Heart Failure With Reduced EjectIon FrAction (VICTORIA)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2016 to 2019Enrolled5,050ConditionsHeart Failure, Chronic Heart Failure With Reduced Ejection FractionArmsVericiguat, Placebo for vericiguat
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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

17 authors.

Palak ShahInova Schar Heart and Vascular, Falls Church, VA (P.S., C.R.d.F., C.M.O.).ORCID 0000-0001-8175-168X
Yinggan ZhengUniversity of Alberta, Canadian VIGOUR Centre, Edmonton, AB, Canada (Y.Z., J.A.E., R.K.S., C.M.W., P.W.A.).ORCID 0009-0009-2246-3683
Burkert PieskeUniversity Medicine Rostock, Germany (B.P.).
Vojtech MelenovskyDepartment of Cardiology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic (V.M.).ORCID 0000-0001-8921-7078
Carolyn S P LamNational Heart Centre Singapore, Duke-National University of Singapore (C.S.P.L.).ORCID 0000-0003-1903-0018
Karen SliwaCape Heart Institute, Faculty of Health Sciences, University of Cape Town, South Africa (K.S.).ORCID 0000-0002-8272-0911
Javed ButlerBaylor Scott and White Research Institute, Dallas, TX (J.B.).ORCID 0000-0001-7683-4720
Justin A EzekowitzUniversity of Alberta, Canadian VIGOUR Centre, Edmonton, AB, Canada (Y.Z., J.A.E., R.K.S., C.M.W., P.W.A.).ORCID 0000-0002-2724-4086
Christopher R deFilippiInova Schar Heart and Vascular, Falls Church, VA (P.S., C.R.d.F., C.M.O.).ORCID 0000-0002-0660-4943
Christopher M O'ConnorInova Schar Heart and Vascular, Falls Church, VA (P.S., C.R.d.F., C.M.O.).
Roopinder K SandhuUniversity of Alberta, Canadian VIGOUR Centre, Edmonton, AB, Canada (Y.Z., J.A.E., R.K.S., C.M.W., P.W.A.).ORCID 0000-0002-2629-3476
Lothar RoessigBayer AG, Wuppertal, Germany (L.R.).
Jasper TrompSaw Swee Hock School of Public Health National University of Singapore (J.T.).ORCID 0000-0001-6043-0713
Cynthia M WesterhoutUniversity of Alberta, Canadian VIGOUR Centre, Edmonton, AB, Canada (Y.Z., J.A.E., R.K.S., C.M.W., P.W.A.).ORCID 0000-0003-1082-5981
Adriaan A VoorsUniversity of Groningen, University Medical Centre Groningen, the Netherlands (A.A.V.).ORCID 0000-0002-5417-4415
Paul W ArmstrongUniversity of Alberta, Canadian VIGOUR Centre, Edmonton, AB, Canada (Y.Z., J.A.E., R.K.S., C.M.W., P.W.A.).ORCID 0000-0002-0460-3445
VICTORIA Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with heart failure and reduced ejection fraction (HFrEF) have a high residual risk for heart failure hospitalizations and cardiovascular death. We aimed to use multimodality data to identify unique HFrEF subgroups with high residual risk.

methodsIn this VICTORIA substudy (Vericiguat Global Study in Subjects With Heart Failure With Reduced Ejection Fraction), clinical, electrocardiographic, echocardiographic, quantitative biomarker, and targeted proteomics data were collected. Agglomerative hierarchical clustering was performed using 105 variables to define HFrEF phenogroups. Cox regression estimated the relationship between the HFrEF phenogroups and the primary composite outcome of cardiovascular death or heart failure hospitalization. External validation of the phenogroups was performed in the BIOSTAT-CHF cohort (Biology Study to Tailored Treatment in Chronic Heart Failure). Multinomial logistic regression identified the most important variables in defining the HFrEF phenogroups.

resultsThere were 564 participants; after clustering, the optimal number of HFrEF phenogroups was 3. Phenogroup 1 was young, well-treated with guideline-directed medical therapy, and least likely to have an implantable cardioverter defibrillator. Phenogroup 2 had the highest prevalence of atrial fibrillation and pathological Q-waves on electrocardiography. Phenogroup 3 was older, had more biventricular dysfunction, and had advanced renal disease. A stepwise increase in the risk of the primary composite outcome was observed from HFrEF phenogroup 1 to 3 (hazard ratio, 7.0 [95% CI, 4.1-12.0];

conclusionsWe identified and externally validated unique HFrEF subpopulations with shared biological characteristics that differentiated residual risk for cardiovascular death or heart failure hospitalization. GDF-15 was the most important protein used to distinguish the 3 HFrEF phenogroups. These findings may inform study entry criteria for future HFrEF trials focused on the development of novel therapeutics. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02861534.

Indexed as

Heart FailureStroke VolumeVentricular Function, LeftAgedBiomarkersEchocardiographyElectrocardiographyFemaleHospitalizationHumansMaleMiddle AgedPhenotypeRisk AssessmentRisk FactorsVictoriaBiomarkerscluster analysisgrowth differentiation factor 15heart failurehospitalizationrisk

Identifiers

PMID41058565
PMCPMC12908639

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Registered trials

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.