Evidence map›Paper›PMID 40191628›Full record

ArticleEuropean heart journal. Case reports2025

Familial cardiac laminopathy with predominant atrial involvement: a case series of a family with

Andreas Müssigbrodt, Romain Vergier, Maria Herrera Bethencourt, Astrid Monfort, Jocelyn Inamo, Veronique Fressart, Pascale Richard, Patrice Bouvagnet

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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Andreas MüssigbrodtDepartment of Cardiology, CHU Martinique (University Hospital of Martinique), BP 632, 97200 Fort de France, France.ORCID https://orcid.org/0000-0003-0748-0302
Romain VergierDepartment of Cardiology, CHU Martinique (University Hospital of Martinique), BP 632, 97200 Fort de France, France.ORCID https://orcid.org/0009-0001-2450-9595
Maria Herrera BethencourtDepartment of Cardiology, CHU Martinique (University Hospital of Martinique), BP 632, 97200 Fort de France, France.
Astrid MonfortDepartment of Cardiology, CHU Martinique (University Hospital of Martinique), BP 632, 97200 Fort de France, France.ORCID https://orcid.org/0000-0002-4432-5566
Jocelyn InamoDepartment of Cardiology, CHU Martinique (University Hospital of Martinique), BP 632, 97200 Fort de France, France.ORCID https://orcid.org/0000-0002-1057-9699
Veronique FressartUnité Fonctionnelle de Cardiogénétique et Myogénétique Moléculaire et Cellulaire, DMU Biogem, Service de Biochimie Métabolique, AP-HP-Sorbonne Université, Pitié-Salpêtrière - Charles Foix, 47-83, boulevard de l'Hôpital, 75651 Paris cedex 13, France.
Pascale RichardUnité Fonctionnelle de Cardiogénétique et Myogénétique Moléculaire et Cellulaire, DMU Biogem, Service de Biochimie Métabolique, AP-HP-Sorbonne Université, Pitié-Salpêtrière - Charles Foix, 47-83, boulevard de l'Hôpital, 75651 Paris cedex 13, France.
Patrice BouvagnetDepartment of Cardiology, CHU Martinique (University Hospital of Martinique), BP 632, 97200 Fort de France, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: We present a case series detailing a family with familial cardiac laminopathy, including the female index patient, her father, her brother, and her daughter, all diagnosed with atrial arrhythmias, i.e. atrial fibrillation (AF), atrial flutter, and atrial premature contractions. Case summary: The index patient is known for frequent premature atrial contractions since the age of 35 years and for persistent AF since the age of 46 years. Rhythm control of symptomatic AF was achieved after two ablations. The brother of the index patient is known for asymptomatic persistent AF since the age of 26 years. He has opted for rate control and oral anticoagulation. Their father had persistent AF for many years before his death. The daughter of the index patient has asymptomatic frequent premature atrial contractions. She is under medical surveillance without specific medical treatment. All four patients have a normal ventricular systolic function. Genetic testing revealed a heterozygous missense variant in the Discussion: The familial occurrence of atrial arrhythmias without significant ventricular involvement in several family members with heterozygous

Indexed as

Atrial fibrillationCase reportLaminopathyLMNAMutation

Identifiers

PMID40191628
PMCPMC11969145

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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.