Evidence map›Paper›PMID 41327012›Full record

Observational studyBMC geriatrics2025

Untangling the prognostic value of diastolic dysfunction, NT-proBNP, and frailty in older patients with preserved left ventricular ejection fraction without valvular disease.

Christophe de Terwangne, Bert Vaes, Agnès Pasquet, Benoit Boland, Anne-Catherine Pouleur, Jean-Marie Degryse

Abstract readObservational Study
In one paragraph

Observational study in BMC geriatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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.

Christophe de TerwangneDivision of Geriatric Medicine, Cliniques Universitaires Saint-Luc - Université Catholique de Louvain, Brussels, 1200, Belgium. Christophe.deterwangne@saintluc.uclouvain.be.
Bert VaesDepartment of Public Health and Primary Care, Katholieke Universiteit Leuven, Leuven, 3000, Belgium.
Agnès PasquetDivision of Cardiology, Cliniques Universitaires Saint-Luc - Université Catholique de Louvain, Brussels, 1200, Belgium.
Benoit BolandDivision of Geriatric Medicine, Cliniques Universitaires Saint-Luc - Université Catholique de Louvain, Brussels, 1200, Belgium.
Anne-Catherine PouleurDivision of Cardiology, Cliniques Universitaires Saint-Luc - Université Catholique de Louvain, Brussels, 1200, Belgium.
Jean-Marie DegryseDepartment of Public Health and Primary Care, Katholieke Universiteit Leuven, Leuven, 3000, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiastolic dysfunction (DD) is a common feature in older adults, but its prognostic value is unclear.

aimThis study aims to assess the ability of DD against NT-proBNP and frailty to predict all-cause mortality, cardiovascular mortality, and a first unplanned hospitalization in older adults.

methodsSecondary analysis of the observational population-based BELFRAIL cohort of patients aged ≥ 80 years with cardiac echography at inclusion. Patients were included if LVEF ≥ 50% and without severe valvular disease. DD was defined if 50% of the criteria of the American Society of Echocardiography were fulfilled (average E/e'>14, septal e' velocity < 7 cm/s or lateral < 10 cm/s, tricuspid velocity > 2.8 m/s, left atrial volume index > 34ml/m

resultsOf the 393 patients (mean age 85 years [SD 3,6], 257 (65%) women), 185 (47%) had DD, 76 (19%) an elevated NT-proBNP, and 50 (13%) were frail. During 5.1 ± 0.2 years, 143 (36%) patients died, of whom 55 (14%) from CV causes. Crude mortality was worse (log-rank p < 0.05) for patients with DD (HR 1.48 [1.07-2.06]), elevated NT-proBNP (2.07 [HR 1.44-2.97]) or frailty (HR 3.02 [2.05-4.47]). After adjustment, DD predicted only CV mortality (HR 1.84 [1.03-3.31]). NT-proBNP predicted both all-cause (HR 1.52 [1.03-2.24]) and CV mortality (HR 2.16 [1.20-3.87]). Frailty predicted all-cause mortality (HR 2.10 [1.38-3.21]) and the first unplanned hospitalization (HR 1.62 [1.08 - 2.42]). Regarding CART, frailty was the root node for both predicting the risk of all-cause mortality and a first unplanned hospitalization. NT-proBNP was the root node in the CV mortality tree, followed by frailty.

conclusionCompared to NT-proBNP and frailty, DD offers limited added value in risk stratification for older people with preserved ejection fraction and no valvular disease. Frailty emerged as the strongest and most consistent predictor of mortality and hospitalization, and was central in the all-cause mortality and hospitalization decision-tree models.

Indexed as

FrailtyNatriuretic Peptide, BrainPeptide FragmentsStroke VolumeVentricular Dysfunction, LeftVentricular Function, LeftAged, 80 and overBiomarkersCohort StudiesDiastoleFemaleHeart Valve DiseasesHospitalizationHumansMalePredictive Value of TestsBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)DiastolicFrailtyNT-proBNPOlderPreserved ejection fraction

Identifiers

PMID41327012
PMCPMC12667101

What Socratic holds

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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 Socratic graph.