PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
May 3, 20263 citations

Prevalence of deleterious variants in cardiomyopathy genes in early-onset atrial fibrillation.

View Full Paper
OVOliver Bundgaard VadQVQuim Bech VilasecaABAstrid Filt Beyer

Key Result

Pathogenic or likely pathogenic variants in cardiomyopathy genes were present in 3.85% to 8.8% of individuals with early-onset atrial fibrillation, compared to 1.03% in those without an AF diagnosis.

Key Points

  • This research aims to identify genetic variants in cardiomyopathy genes among individuals with early-onset atrial fibrillation.
  • Conducted targeted sequencing of cardiomyopathy genes in 478 Danish individuals with early AF onset.
  • Analyzed whole exome sequencing data from 375,869 individuals in the UK Biobank, including those with AF.
  • 8.8% of Danish individuals with early-onset AF carried pathogenic or likely pathogenic variants in cardiomyopathy genes.
  • Rare pathogenic variants were found in 3.85% of individuals with early AF in the UK Biobank, compared to 1.03% without a diagnosis.

Study Design

Type

Observational (n=376,347)

Multicenter

Yes

Structured PICO

Is early-onset atrial fibrillation associated with an increased prevalence of pathogenic variants in cardiomyopathy genes?

P
Population
478 individuals from a Danish cohort with early atrial fibrillation (AF) onset, and 375,869 individuals from the UK Biobank (including 29,267 individuals with AF).
I
Intervention
Targeted sequencing and whole exome sequencing of 34 cardiomyopathy-associated genes
C
Comparator
Individuals without an AF diagnosis (within the UK Biobank cohort)
O
Outcome
Prevalence of pathogenic or likely pathogenic (P/LP) variants in cardiomyopathy-associated genessurrogate

Early-onset atrial fibrillation is associated with a higher prevalence of pathogenic variants in cardiomyopathy genes, suggesting a potential role for genetic testing in this population.

Main Result

Absolute Event Rate: 3.85% vs 1.03%

Abstract

Atrial fibrillation (AF) is a common cardiac arrhythmia associated with an increased risk of stroke, heart failure, and death. Recent studies suggest that early-onset AF increases the risk of developing heart failure and dilated cardiomyopathy. This study aimed to identify genetic variants in a large set of 34 cardiomyopathy genes among early-onset AF individuals. We conducted targeted sequencing of cardiomyopathy-associated genes in 478 individuals from a Danish cohort with early AF onset. Additionally, we analyzed whole exome sequencing data from 375,869 individuals from the UK Biobank, including 29,267 individuals with AF. Of the Danish individuals with early-onset AF, 8.8% carried pathogenic or likely pathogenic (P/LP) variants in cardiomyopathy-associated genes. The prevalence of rare P/LP variants in the UK Biobank analysis ranged from 3.85% in the group with early AF onset to 1.03% in the group without AF diagnosis. Results were largely consistent when excluding individuals with no prior cardiomyopathy or heart failure diagnosis. This suggests that genetic testing for cardiomyopathy could be relevant in selected individuals with early AF diagnosis.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Vad et al. (2026) conducted an observational in Early-onset atrial fibrillation (n=376,347). Genetic testing for cardiomyopathy genes vs. Individuals without AF diagnosis was evaluated on Prevalence of pathogenic or likely pathogenic (P/LP) variants in cardiomyopathy-associated genes. Pathogenic or likely pathogenic variants in cardiomyopathy genes were present in 3.85% to 8.8% of individuals with early-onset atrial fibrillation, compared to 1.03% in those without an AF diagnosis.

synapsesocial.com/papers/69f6e6ab8071d4f1bdfc7751https://doi.org/10.1038/s41431-026-02119-5
Ask AI
Helpful
Bookmark
Share
View Full Paper