Identification of a Genetic Locus for Familial Atrial Fibrillation
Ramon Brugada, M.D., Terry Tapscott, B.S., Grazyna Z. Czernuszewicz, M.S., A.J. Marian, M.D., Anna Iglesias, B.S., Lluis Mont, M.D., Josep Brugada, M.D., Josep Girona, M.D., Anna Domingo, M.D., Linda L. Bachinski, Ph.D., and Robert Roberts, M.D.
Background Atrial fibrillation, the most common sustained cardiac-rhythmdisturbance, affects over 2 million Americans and accounts forone third of all strokes in patients over 65 years of age. Themolecular basis for atrial fibrillation is unknown, and palliativetherapy is used to control the ventricular rate and preventsystemic emboli. We identified a family of 26 members of whom10 had atrial fibrillation that segregated as an autosomal dominantdisease. We subsequently identified two additional familiesin which the disease was linked to the same locus.
Methods We screened the human genome with 300 polymorphic dinucleotide-repeatmarkers using an unconventional strategy of pooling the DNAsamples into two groups (affected and unaffected), which reducedthe sample size by approximately 90 percent, before performinglinkage analysis to map the locus. This made it possible toidentify potential loci within a few weeks.
Results The lod scores for markers D10S569 and D10S607, locatedat 10q22q24, were 3.60 in Family 1. The disease locusin Families 2 and 3 was also linked to the same markers, withlod scores of 6.02 and 5.35 for markers D10S569 and D10S607,respectively, when data on all three families were combined.Haplotype analysis of the three families showed that the locuswas between D10S1694 and D10S1786, an interval of 11.3 centimorgans.
Conclusions Identification of the gene for familial atrial fibrillationwill help to elucidate the molecular basis of the disease andprovide insights into acquired forms. The strategy of poolingDNA samples for analysis is more time and cost effective thanconventional screening and should accelerate the process ofgene mapping in the future.
Source Information
From the Department of Cardiology, Baylor College of Medicine, Houston (R.B., T.T., G.Z.C., A.J.M., A.I., L.L.B., R.R.); the Cardiac Arrhythmia Service, Department of Cardiology, Hospital Clinic, University of Barcelona, Barcelona, Spain (L.M., J.B.); and the Department of Cardiology, Hospital MaternoInfantil Vall d'Hebron, Barcelona, Spain (J.G., A.D.).
Address reprint requests to Dr. Roberts at Baylor College of Medicine, 6550 Fannin, MS SM677, Houston, TX 77030.
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