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Published on: February 26, 2013
Outcomes Associated With Familial Versus Nonfamilial Atrial Fibrillation: A Matched Nationwide Cohort Study
Anna Gundlund1, Jonas Bjerring Olesen2, Laila Staerk2
1Department of Cardiology, Copenhagen University Hospital Herlev-Gentofte, Hellerup, Denmark annagundlund@gmail.com.
Insights
Familial atrial fibrillation (AF) increases AF risk, but once diagnosed, long-term death and thromboembolism risks are similar to nonfamilial AF. This finding impacts patient management and risk stratification strategies.
Area of Science:
- Cardiology
- Genetics
- Public Health
Background:
- Atrial fibrillation (AF) is a common arrhythmia.
- A family history of AF is a known risk factor for developing the condition.
- The long-term outcomes for patients with familial AF compared to nonfamilial AF are not well-established.
Purpose of the Study:
- To compare all-cause mortality and long-term thromboembolic risk in patients with and without familial atrial fibrillation (AF).
Main Methods:
- Danish nationwide registry data (1995-2012) identified AF patients.
- Patients were divided into familial AF and nonfamilial AF groups.
- 1:1 matching based on age, sex, and AF diagnosis year was performed.
- Cumulative incidence and multivariable Cox models analyzed long-term outcomes.
Main Results:
- 8658 AF patients (4329 matched pairs) were analyzed.
- Familial AF patients had similar CHA2DS2-VASc scores and slightly fewer comorbidities than nonfamilial AF patients.
- No significant difference in the risk of death (aHR 0.91) or thromboembolism (aHR 0.90) was observed between familial and nonfamilial AF groups.
Conclusions:
- While a family history increases AF susceptibility, AF diagnosis equalizes long-term risks.
- Long-term mortality and thromboembolic event risks are comparable between familial and nonfamilial AF patients.
- These findings suggest that once AF is established, its genetic predisposition may not significantly alter subsequent major adverse cardiovascular outcomes.
Background:
We examined all-cause mortality and long-term thromboembolic risk (ischemic stroke, transient ischemic attack, systemic thromboembolism) in patients with and without familial atrial fibrillation (AF).
Methods And Results:
Using Danish nationwide registry data, we identified all patients diagnosed with AF (1995-2012) and divided them into those with familial AF (having a first-degree family member with a prior AF admission) and those with nonfamilial AF. We paired those with and without familial AF according to age, year of AF diagnosis, and sex in a 1:1 match. Using cumulative incidence and multivariable Cox models, we examined the risk of long-term outcomes. We identified 8658 AF patients (4329 matched pairs) with and without familial AF. The median age was 50 years (interquartile range 43-54 years), and 21.4% were women. Compared with nonfamilial AF patients, those with familial AF had slightly less comorbid illness but similar overall CHA2DS2-VASc score (P=0.155). Median follow-up was 3.4 years (interquartile range 1.5-6.5 years). Patients with familial AF had risk of death and thromboembolism similar to those with nonfamilial AF (adjusted hazard ratio 0.91 [95% CI 0.79-1.04] for death and 0.90 [95% CI 0.71-1.14] for thromboembolism).
Conclusions:
Although family history of AF is associated with increased likelihood for development of AF, once AF developed, long-term risks of death and thromboembolic complications were similar in familial and nonfamilial AF patients.
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