Evidence map›Paper›PMID 41858107›Full record

ReviewEuropean heart journal2026

Genetic counselling implementation in dilated cardiomyopathy.

Job A J Verdonschot, Karin Y van Spaendonck-Zwarts, Debby M E I Hellebrekers, Folkert W Asselbergs, Elijah R Behr, Philippe Charron, Dana Dawson, Pablo Garcia-Pavia, Kristina H Haugaa, Ruxandra Jurcut and 15 more

Abstract readReview
In one paragraph

Review in European heart journal, 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

25 authors.

Job A J VerdonschotDepartment of Clinical Genetics, Maastricht University Medical Center+, P. Debyelaan 25, Maastricht 6229HX, The Netherlands.ORCID 0000-0001-5549-1298
Karin Y van Spaendonck-ZwartsDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Debby M E I HellebrekersDepartment of Clinical Genetics, Maastricht University Medical Center+, P. Debyelaan 25, Maastricht 6229HX, The Netherlands.
Folkert W AsselbergsDepartment of Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
Elijah R BehrCardiovascular and Genomics Research Institute, City St. George's, University of London, London, UK.
Philippe CharronFilière Nationale de Santé CARDIOGEN, Paris, France.
Dana DawsonAberdeen Cardiovascular and Diabetes Centre, University of Aberdeen, Aberdeen, UK.ORCID 0000-0003-2815-4469
Pablo Garcia-PaviaHeart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro IDIPHISA, Madrid, Spain.
Kristina H HaugaaDepartment of Cardiology, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-4900-0453
Ruxandra JurcutExpert Center for Genetic Cardiovascular Diseases, Emergency Institute for Cardiovascular Diseases 'Prof. Dr. C.C. Iliescu', University of Medicine and Pharmacy 'Carol Davila', Bucharest, Romania.ORCID 0000-0002-3438-2612
Petr Kuchynka2nd Department of Medicine, Department of Cardiovascular Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
Luis R LopesBarts Heart Centre, St Bartholomew's Hospital, London, UK.
Andrea MazzantiMolecular Cardiology Unit, IRCCS Istituti Clinici Scientifici Maugeri, Pavia, Italy.
Marco MetraCardiology, ASST Spedali Civili di Brescia, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy.
Lorenzo MonserratMedical Department, Dilemma Solutions, A Coruña, Spain.
Juan Pablo KaskiCentre for Paediatric Inherited and Rare Cardiovascular Disease, University College London, Institute of Cardiovascular Science, London, UK.ORCID 0000-0002-0014-9927
Antonis PantazisDepartment of Cardiology, Royal Brompton and Harefield Hospitals, London, UK.
Sanjay K PrasadDepartment of Cardiology, Royal Brompton and Harefield Hospitals, London, UK.ORCID 0000-0002-5637-0727
Giuseppe RosanoCardiovascular Clinical Academic Group, St. George's University Hospitals NHS Foundation Trust, London, UK.ORCID 0000-0003-4023-2263
Petar M SeferovicDepartment of Cardiology, Serbian Academy of Sciences and Arts and Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Mary N SheppardCRY Cardiovascular Pathology Unit, Cardiovascular and Genetic Research Institute, St.George's, University of London, London, UK.
Gianfranco SinagraCardiothoracovascular Department, Azienda Sanitaria Universitaria Giuliano Isontina, Center for Cardiomyopathies, University of Trieste, Trieste, Italy.
Maria Teresa Tome EstebanCardiovascular and Genomics Research Institute, City St. George's, University of London, London, UK.
Stephane R B HeymansDepartment of Cardiology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.
J Peter van TintelenDepartment of Genetics, University Medical Center Utrecht, Heidelberglaan 100, Utrecht 3584CX, The Netherlands.

Funding

Clinical Scientist DekkerDutch Heart Foundation 03-005-2022-0040ZonMW Veni
6 · The paper itself

Abstract

Genetic testing has become an integral part of the diagnostic workup of patients with dilated cardiomyopathy (DCM). While the initial goal of genetic testing was to identify family members at risk, recent advances have now extended their relevance to clinical decision-making. Our knowledge of the genetic architecture of DCM has expanded significantly, promoting a shift from the monogenic dogma towards a broader polygenic spectrum. However, current genetic testing strategies still primarily rely on the model of monogenic inheritance with an incomplete penetrance. Large studies have shown a yield varying from 8% to 36% of genetic testing in patients with DCM, depending on aetiology or family history. Genetic testing is generally warranted for every patient with DCM where genetic results could have an impact on risk stratification, the prognosis or the treatment of the patient, or its family members with an opportunity for reassurance or early disease detection. There are various strategies for genetic testing including broad multigene panels, or more targeted panels limited to specific disease-associated genes. Identified variants are classified by genetic laboratories, where pathogenic or likely pathogenic variants often have actionable clinical implications. It is crucial to interpret these variants in the context of the individual patient considering the phenotype and other contributing factors. When the genetic results are consistent with the patients' broader phenotype, potential clinical implications may include decision for device therapy, recommendations for family screening, and reproductive options. A comprehensive approach to integrate genetic testing in the clinical care of patients with DCM is proposed.

Indexed as

Cardiomyopathy, DilatedGenetic CounselingGenetic Predisposition to DiseaseGenetic TestingHumansPhenotypeDilated cardiomyopathyGenetic testingPathogenic variant

Identifiers

PMID41858107
PMCPMC13286647

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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.