Evidence map›Paper›PMID 42489227›Full record

ArticleThe Journal of physiology2026

Ultrasound-based haemodynamic force trajectories in a murine model of reversible pressure overload.

Peyton M Day, Thomas Moore-Morris, Craig J Goergen, Pierre Sicard

Abstract read
In one paragraph

Article in The Journal of physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

4 authors.

Peyton M DayWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana, USA.
Thomas Moore-MorrisUniversité de Montpellier, INSERM, CNRS, IGF, Montpellier, France.
Craig J GoergenWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana, USA.ORCID https://orcid.org/0000-0001-8883-7953
Pierre SicardUniversité de Montpellier, INSERM, CNRS, PhyMedExp, Montpellier, France.ORCID https://orcid.org/0000-0001-5837-3916

Funding

Agence Nationale de la Recherche ANR-11-INBS-0006Fulbright U.S. Scholar Program
6 · The paper itself

Abstract

Haemodynamic forces (HDF) quantify intraventricular pressure gradients as integrated vectors derived from myocardial motion and blood flow, providing a sensitive marker of left ventricular (LV) remodelling beyond conventional metrics such as ejection fraction or strain. Although HDF analysis has been clinically validated in heart failure, it remains underexplored in preclinical models. To determine whether HDF metrics derived from high-resolution murine echocardiography can sensitively track cardiac dysfunction and predict functional recovery, male mice (n = 8) underwent serial echocardiography at baseline, after transverse aortic constriction (TAC) and 4 weeks after aortic debanding (deTAC). LV function and interval-specific HDF components were quantified, including longitudinal and transverse forces over predefined systolic and diastolic windows. Longitudinal interval-based parameters emerged as sensitive, integrative markers of LV dysfunction after TAC and deTAC. Notably, a novel exploratory waveform, early-to-late systolic impulse longitudinal HDF ratio, showed the strongest associations with pressure overload and subsequent functional recovery (baseline vs. TAC: P < 0.001; TAC vs. deTAC: P = 0.003; baseline vs. deTAC: P = 0.049). By contrast, diastolic HDF indices, including the previously proposed longitudinal e‑wave ratio, did not significantly differentiate between time points. Transverse HDF over the systolic impulse interval further demonstrated potential for predicting post‑surgical recovery following unloading. These findings support systolic HDF metrics, particularly longitudinal and transverse interval‑based parameters, as sensitive integrative markers of LV dysfunction and reverse remodelling in preclinical pressure‑overload models, and highlight their translational relevance for echocardiography‑based HDF analysis. KEY POINTS: Haemodynamic force (HDF) analyses evaluate intraventricular pressure gradients as integrated vectors of myocardial motion and blood flow, providing complementary markers of pump (in)efficiency beyond ejection fraction or strain. High-resolution murine echocardiography enables robust derivation of interval-specific HDF metrics. Systolic HDF metrics, particularly transverse components during impulse intervals, showed potential for predictive power correlating with cardiac recovery. Systolic HDF reflect key changes in force generation and intraventricular flow during pressure overload, allowing early detection of maladaptive remodelling and treatment response, with translational potential for non-invasive risk stratification in aortic stenosis patients.

Indexed as

HemodynamicsVentricular Dysfunction, LeftAnimalsDisease Models, AnimalEchocardiographyHeart FailureMaleMiceMice, Inbred C57BLVentricular Function, LeftVentricular Remodelinghaemodynamic forcesheart failurepressure overloadstrainunloading

Identifiers

PMID42489227
PMCPMC13532889

What OpenQuestion 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 OpenQuestion graph.