Evidence map›Paper›PMID 41903171›Full record

Trial reportJAMA cardiology2026

Biomarker, Functional Status, and Quality-of-Life Trajectories Before Modes of Death in Heart Failure: Post Hoc Analysis of the FINEARTS-HF Randomized Clinical Trial.

Henri Lu, Annamaria Kosztin, Brian L Claggett, Alberto Foà, Maria A Pabón, Akshay S Desai, Pardeep S Jhund, Alasdair D Henderson, Bela Merkely, Carolyn S P Lam and 12 more

Registry-linked trialAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in JAMA cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04435626 (A Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of Finerenone on Morbidity and Mortality in Participants With Heart Failure), which is not on this map. Not yet cited in PubMed.

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

NCT04435626 phase3completednot on this map

A Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of Finerenone on Morbidity and Mortality in Participants With Heart Failure (NYHA II-IV) and Left Ventricular Ejection Fraction ≥ 40% (LVEF ≥ 40%)

TypeinterventionalSponsorBayerRan2020 to 2024Enrolled6,016ConditionsHeart FailureArmsFinerenone (BAY94-8862), Placebo
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

5 · Who and what money

Authors and funding

22 authors.

Henri LuDivision of Cardiology, Lausanne University Hospital, University of Lausanne, Lausanne, Vaud, Switzerland.
Annamaria KosztinSemmelweis University, Heart and Vascular Center, Budapest, Hungary.
Brian L ClaggettDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Alberto FoàDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Maria A PabónDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Akshay S DesaiDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Pardeep S JhundUniversity of Glasgow, Glasgow, Scotland, United Kingdom.
Alasdair D HendersonUniversity of Glasgow, Glasgow, Scotland, United Kingdom.
Bela MerkelySemmelweis University, Heart and Vascular Center, Budapest, Hungary.
Carolyn S P LamNational Heart Centre Singapore & Duke-National University of Singapore, Singapore.
Michele SenniUniversity of Milano-Bicocca ASST Papa Giovanni XXIII Hospital, Bergamo, Italy.
Sanjiv J ShahNorthwestern University Feinberg School of Medicine, Chicago, Illinois.
Adriaan A VoorsUniversity of Groningen, Groningen, the Netherlands.
Faiez ZannadUniversity of Lorraine, Nancy, France.
Bertram PittUniversity of Michigan, Ann Arbor.
Flaviana AmaranteCardiology and Nephrology Clinical Development, Bayer SA, São Paulo, Brazil.
Riitta SaarinenBayer AG, Global Medical Affairs, Berlin, Germany.
Yoriko De SanctisBayer U.S. LLC, Research & Development, Pharmaceuticals, Whippany, New Jersey.
Andrea GlasauerBayer AG, Global Medical Affairs, Berlin, Germany.
John J V McMurrayUniversity of Glasgow, Glasgow, Scotland, United Kingdom.
Muthiah VaduganathanDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Scott D SolomonDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Sudden death remains a leading cause of mortality in patients with heart failure with mildly reduced ejection fraction (HFmrEF) or HF with preserved ejection fraction (HFpEF), but whether these events are preceded by clinical deterioration remains unclear. Objective: To characterize clinical trajectories preceding sudden death in patients with HFmrEF or HFpEF and compare them with trajectories before other modes of death and survival. Design, Setting, and Participants: This was a post hoc analysis of the Finerenone Trial to Investigate the Efficacy and Safety Superior to Placebo in Patients With Heart Failure (FINEARTS-HF) randomized clinical trial evaluating trajectories of functional status, patient-reported health status, and natriuretic peptide levels preceding adjudicated modes of death. This was a global, event-driven clinical trial. Patients with symptomatic HF, left ventricular EF of 40% or greater, New York Heart Association class (NYHA) II to IV, and elevated N-terminal pro-B-type natriuretic peptide (NT-proBNP) were enrolled between September 14, 2020, and January 10, 2023. Data analysis was conducted in December 2025. Interventions: Finerenone vs placebo. Main Outcomes and Measures: Longitudinal trajectories of NYHA class, Kansas City Cardiomyopathy Questionnaire Total Symptom Score (KCCQ-TSS), and NT-proBNP levels preceding sudden death were compared with trajectories in survivors and those who died of HF-related, nonsudden cardiovascular, or noncardiovascular causes, using linear mixed-effects models with restricted cubic splines. Results: Included in this analysis were 6001 patients (mean [SD] age, 72.0 [9.6] years; 3269 male [54%]). Over a median (IQR) follow-up of 2.7 (1.9-3.0) years, 215 sudden deaths occurred. In the 6 months before death, sudden death was preceded by a slight worsening in physician-assigned NYHA class (from approximately 2.3 to 2.4), worsening self-reported health status (an approximately 8-point decline in KCCQ-TSS), and a gradual rise in NT-proBNP levels (from approximately 1800 to 2000 pg/mL). In contrast, among patients who survived, NYHA class improved (from approximately 2.3 to 2.1), KCCQ-TSS increased (from approximately 68 to 77), and NT-proBNP levels declined (from approximately 800 to 650 pg/mL) over the 18 months before the end of follow-up. Comparable patterns of deterioration to those preceding sudden death, often more pronounced, were observed before other modes of death. Conclusions and Relevance: Results of this post hoc analysis of the FINEARTS-HF randomized clinical trial reveal that in this contemporary HFmrEF or HFpEF cohort, sudden death was preceded by modest worsening of symptoms, declining quality of life, and rising natriuretic peptide levels, suggesting many of these events may not have been entirely sudden. However, similar deterioration preceding other modes of death suggests limited specificity for sudden death. Trial Registration: ClinicalTrials.gov Identifier: NCT04435626.

Indexed as

Death, Sudden, CardiacHeart FailureNatriuretic Peptide, BrainPeptide FragmentsQuality of LifeAgedBiomarkersFemaleFunctional StatusHumansMaleMiddle AgedStroke VolumeBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)

Identifiers

PMID41903171
PMCPMC13033172

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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.