Literature DB >> 19808493

Familial aggregation of atrial fibrillation: a study in Danish twins.

Ingrid Elisabeth Christophersen1, Lasse Steen Ravn, Esben Budtz-Joergensen, Axel Skytthe, Stig Haunsoe, Jesper Hastrup Svendsen, Kaare Christensen.   

Abstract

BACKGROUND: Heritability may play a role in nonfamilial atrial fibrillation (AF). We hypothesized that a monozygotic (MZ) twin whose co-twin was diagnosed with AF would have an increased risk of the disease compared with a dizygotic (DZ) twin in the same situation. METHODS AND
RESULTS: A sample of 1137 same-sex twin pairs (356 MZ and 781 DZ pairs) in which one or both members were diagnosed with AF were identified in The Danish Twin Registry. Concordance rates were twice as high for MZ pairs than for DZ pairs regardless of sex (22.0% versus 11.6%, P<0.0001). In a Cox regression of event-free survival times, we compared the time span between occurrences of disease in MZ and DZ twins. The unaffected twin was included when his or her twin-sibling (the index twin) was diagnosed with AF. After adjustment for age at entry, MZ twins had a significantly shorter event-free survival time (hazard ratio, 2.0; 95% CI, 1.3 to 3.0), thereby indicating a genetic component. Using biometric models, we estimated the heritability of AF to be 62% (55% to 68%), due to additive genetics. There were no significant differences across sexes.
CONCLUSIONS: All the analyses of twin similarities in the present study indicate that genetic factors play a substantial role in the risk of AF for both sexes. The recurrence risk for co-twins (12% to 22%) is clinically relevant and suggests that co-twins of AF-affected twins belong to a high-risk group for AF.

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Year:  2009        PMID: 19808493      PMCID: PMC2760022          DOI: 10.1161/CIRCEP.108.786665

Source DB:  PubMed          Journal:  Circ Arrhythm Electrophysiol        ISSN: 1941-3084


  24 in total

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Journal:  Twin Res       Date:  2002-10

Review 2.  When assessing twin concordance, use the probandwise not the pairwise rate.

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4.  Identification of a genetic locus for familial atrial fibrillation.

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Review 8.  Atrial fibrillation: natural history, complications, and management.

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9.  Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.

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Review 9.  Genomics of Atrial Fibrillation.

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Journal:  Heart Rhythm       Date:  2013-11-14       Impact factor: 6.343

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