Evidence map›Paper›PMID 42182092›Full record

ArticleEuropean heart journal. Imaging methods and practice2026

Study design and rationale of the Visualizing Subclinical Myocardial Changes with Shear Wave Elastography in Dilated Cardiomyopathy (VISUALIZE-DCM) trial.

Max F G H M Venner, Luuk van Knippenberg, Astrid B M Heymans, Lorenzo Bianchi, Anne G Raafs, Sebastian Streukens, Martijn Smulders, Casper Mihl, Nina J Beelen, Martina Luzzi and 11 more

Abstract read
In one paragraph

Article in European heart journal. Imaging methods and practice, 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
–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

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

21 authors.

Max F G H M VennerDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0009-0001-2574-6672
Luuk van KnippenbergDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.
Astrid B M HeymansDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0009-0008-0030-6444
Lorenzo BianchiDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.
Anne G RaafsDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0001-9228-8045
Sebastian StreukensDepartment of Cardiology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Martijn SmuldersDepartment of Cardiology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Casper MihlDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0003-1348-6970
Nina J BeelenDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0009-0008-0605-4604
Martina LuzziDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.
Sophie L V M StroeksDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.
Joost LumensDepartment of Biomedical Engineering, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0001-8129-7384
Jos HabetsDepartment of Cardiology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Christian KnackstedtDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0002-5457-3010
Guilielmus H J M EllenbroekDepartment of Cardiology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Kevin VernooyDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0002-8818-5964
Vanessa P M van EmpelDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0002-6864-0296
Massimo MischiDepartment of Electrical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.
Stephane R B HeymansDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0001-9477-7803
Ruud J G van SlounDepartment of Electrical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.
Job A J VerdonschotDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands.ORCID https://orcid.org/0000-0001-5549-1298

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac fibrosis is a key disease hallmark of dilated cardiomyopathy (DCM) and is associated with a risk of malignant arrhythmias and sudden cardiac death. Fibrosis can be the earliest sign of disease in asymptomatic family members carrying pathogenic variants, making timely recognition essential. Although echocardiography is often used for family screening, conventional echocardiography cannot assess myocardial tissue characteristics such as fibrosis. Cardiac magnetic resonance imaging (CMR), the reference standard for detecting myocardial fibrosis, provides tissue characterization but is challenging to be used as a first-line screening for all at-risk family members. Shear wave elastography (SWE) using high-frame rate echocardiography is an emerging technique that enables assessment of myocardial stiffness as a surrogate for fibrosis. The VISUALIZE-DCM trial is an investigator-initiated, single-center prospective study that evaluates SWE as a triage tool for CMR to detect myocardial fibrosis, and to determine whether increased myocardial stiffness is an early feature of genetic DCM. In this study, both naturally occurring and acoustic generated shear wave speeds (SWS) are assessed using high-frame rate imaging. Natural shear waves arise during valvular closure, whereas generated shear waves are induced by the acoustic radiation force. Myocardial stiffness measurements derived from SWS will be obtained in patients with established DCM, their at-risk family members, and healthy volunteers. SWE findings will be compared with fibrosis patterns on CMR, evaluated for their ability to detect early disease development in relatives, and contrasted with reference values from healthy controls to determine their potential clinical utility in DCM screening and risk stratification.

Indexed as

clinical trialdilated cardiomyopathyechocardiographyelastographyfamily membersscreening

Identifiers

PMID42182092
PMCPMC13193581

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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.