Familial atrial fibrillation

Familial atrial fibrillation

Eighteen types of familial atrial fibrillation (AF) has been described in the OMIM (Online Mendelian Inheritance in Man) database.

Type of AF Chromosome Gene
ATFB1 10q22-q24  
ATFB2 6q  
ATFB3 11 KCNQ1
ATFB4 21 KCNE2
ATFB5 4q25  
ATFB6 1p36-p35 NPPA
ATFB7 12p13 KCNA5
ATFB8 16q22  
ATFB9 17q24.3 KCNJ2
ATFB10 3p21 SCN5A
ATFB11 1q21.1 GJA5
ATFB12 12p12.1 ABCC9
ATFB13 19q13.11 SCN1B
ATFB14 11q23.3 SCN2B
ATFB15 5p13.2 NUP155
ATFB16 (BRGDA7) 11q24.1 SCN3B
ATFB17 (LQT10) 11q23.3 SCN4B
ATFB18 17q21.32 MYL4

One of the early reports identifying a genetic locus for familial AF was by R Brugada, T Tapscott, G Z Czernuszewicz, A J Marian, A Iglesias, L Mont, J Brugada, J Girona, A Domingo, L L Bachinski and R Roberts [1], in which ten members spanning over three generations had an autosomal dominant pattern. Nine of them had chronic atrial fibrillation while one had paroxysmal atrial fibrillation.

It may be noted that gene for ATFB16 is same as that for BRGA7. That for ATFB17 is the same as that for LQT10. These are heterozygous mutations.

Reference

  1. R Brugada, T Tapscott, G Z Czernuszewicz, A J Marian, A Iglesias, L Mont, J Brugada, J Girona, A Domingo, L L Bachinski, R Roberts. Identification of a genetic locus for familial atrial fibrillation. N Engl J Med. 1997 Mar 27;336(13):905-11.