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.

Human Genetics
|September 1, 2005
PubMed

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.

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