Evidence map›Paper›PMID 41424653›Full record

ArticleEuropean heart journal. Case reports2025

Preimplantation genetic testing for cardiomyopathies: a case series illustrating the clinical and technological perspective.

Isa M E Faassen, Malou Heijligers, Nadine H N Weijermans, Marianne L van Buul-van Zwet, Carlijn S Zietse, Masoud Zamani Esteki, Aimee D C Paulussen, Job A J Verdonschot

Abstract readCase Reports
In one paragraph

Article in European heart journal. Case reports, 2025. 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

8 authors.

Isa M E FaassenDepartment of Cardiology, Maastricht University, Cardiovascular Research Institute Maastricht (CARIM), Universiteitssingel 50, Maastricht 6229 ER, The Netherlands.ORCID https://orcid.org/0009-0009-4784-6189
Malou HeijligersDepartment of Clinical Genetics, Maastricht University Medical Center, P. Debyelaan 25, Maastricht 6229 HX, The Netherlands.ORCID https://orcid.org/0000-0002-0174-8278
Nadine H N WeijermansDepartment of Obstetrics and Gynecology, Maastricht University Medical Center, P. Debyelaan 25, Maastricht 6229 HX, The Netherlands.ORCID https://orcid.org/0000-0002-2865-3738
Marianne L van Buul-van ZwetDepartment of Obstetrics and Gynecology, University Medical Center Utrecht, Heidelberglaan 100, Utrecht 3584 CX, The Netherlands.
Carlijn S ZietseDepartment of Obstetrics and Gynecology, University Medical Center Amsterdam, Meibergdreef 9, Amsterdam 1105 AZ, The Netherlands.
Masoud Zamani EstekiDepartment of Clinical Genetics, Maastricht University Medical Center, P. Debyelaan 25, Maastricht 6229 HX, The Netherlands.ORCID https://orcid.org/0000-0003-3909-0050
Aimee D C PaulussenDepartment of Clinical Genetics, Maastricht University Medical Center, P. Debyelaan 25, Maastricht 6229 HX, The Netherlands.ORCID https://orcid.org/0000-0002-1661-7625
Job A J VerdonschotDepartment of Cardiology, Maastricht University, Cardiovascular Research Institute Maastricht (CARIM), Universiteitssingel 50, Maastricht 6229 ER, The Netherlands.ORCID https://orcid.org/0000-0001-5549-1298

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Preimplantation genetic testing (PGT) is increasingly used in patients with inherited cardiac disease. Technological advances have expanded its applicability, yet the process remains highly individualized and complex. Case summary: We present a case series of four patients undergoing PGT for various cardiogenetic disorders. The cases illustrate technical developments evolving from polymerase chain reaction (PCR) to whole genome sequencing (WGS). Each case highlights distinct aspects of the PGT process to illustrate the steps: (i) the variability in disease penetrance, (ii) the clinical decision-making process, (iii) the duration and timeline of the trajectory, and (iv) the sequencing methodology. Discussion: These cases emphasize the importance of selecting patients who will benefit the greatest risk reduction from PGT, reflecting the significance of individual assessment per couple. Additionally, clinicians should be aware and discuss the possibility of PGT with eligible patients consistently to ensure a comprehensive understanding of their reproductive options.

Indexed as

CardiogeneticsCase seriesPGTReproductive medicine

Identifiers

PMID41424653
PMCPMC12715505

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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.