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Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Familial aggregation in lone atrial fibrillation
Patrick T Ellinor1, Danita M Yoerger, Jeremy N Ruskin
1Cardiac Arrhythmia Service, Massachusetts General Hospital, 149 13th Street, 4th Floor, Charlestown, Boston, MA, 02129, USA.
Insights
Genetic factors significantly increase the risk of developing lone atrial fibrillation (AF). Family members of individuals with AF have a substantially higher chance of developing this common heart arrhythmia.
Area of Science:
- Cardiology
- Genetics
- Epidemiology
Background:
- Atrial fibrillation (AF) is the most prevalent clinical arrhythmia.
- AF is a primary risk factor for stroke.
- Understanding genetic contributions to AF is crucial for risk assessment.
Purpose of the Study:
- To investigate the extent of familial aggregation in lone atrial fibrillation.
- To estimate the relative risk of AF among family members of affected individuals.
- To explore the potential Mendelian genetic contribution to lone AF.
Main Methods:
- Comparative prevalence study.
- Analysis of AF prevalence in relatives of lone AF probands.
- Comparison with age- and sex-matched general population data.
Main Results:
- Family members exhibited significantly increased relative risks for AF.
- Specific risk ratios were calculated for sons, daughters, brothers, sisters, mothers, and fathers.
- For example, brothers had a risk ratio of 70 (95% CI: 47-102).
Conclusions:
- Relatives of individuals with lone AF face a substantially elevated risk of developing the condition.
- These findings suggest a significant Mendelian genetic component in the etiology of lone atrial fibrillation.
- Genetic predisposition plays a key role in the development of this common cardiac arrhythmia.
Abstract:
Atrial fibrillation (AF) is the most common clinical arrhythmia and a major risk factor for stroke. To investigate the role of genetic factors in a typical clinical population, we determined the extent of familial aggregation in patients with lone AF. To estimate the relative risk to family members, the prevalence of AF for each class of relative was compared to the prevalence in the comparable age and sex group from the general population. Family members had an increased relative risk of AF compared to the general population (risk ratio; 95% confidence intervals): sons (8.1; 2.0-32), daughters (9.5; 1.3-67), brothers (70; 47-102), sisters (34; 14-80), mothers (4.0; 2.5-6.5) and fathers (2.0; 1.2-3.6). Relatives of probands with lone AF are at a substantially increased risk of developing this arrhythmia suggesting a Mendelian genetic contribution to the etiology of this common trait.
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