Author/Authors :
Gourraud، نويسنده , , Jean-Baptiste and Le Scouarnec، نويسنده , , Solena and Sacher، نويسنده , , Frederic and Chatel، نويسنده , , Stéphanie and Derval، نويسنده , , Nicolas and Portero، نويسنده , , Vincent and Chavernac، نويسنده , , Pascal and Sandoval، نويسنده , , Juan E. and Mabo، نويسنده , , Philippe and Redon، نويسنده , , Richard and Schott، نويسنده , , Jean-Jacques and Le Marec، نويسنده , , Hervé and Haïssaguerre، نويسنده , , Michel and Probst، نويسنده , , Vincent، نويسنده ,
Abstract :
Objectives
m of this study was to identify families affected by early repolarization syndrome (ERS) and to determine the mode of transmission of the disease.
ound
repolarization (ER) has recently been linked to idiopathic ventricular fibrillation. Familial inheritance of the disease has been suggested but not demonstrated.
s
eened relatives of 4 families affected by ERS. ER was defined as a distinct J-wave in at least 2 consecutive leads and a 1-mm amplitude above baseline. The Valsalva maneuver was performed in affected and unaffected family members to decrease heart rate and thus increase or reveal an ER pattern.
s
-two sudden cardiac deaths occurred in the 4 families including 10 before 35 years of age. In the 4 families, the prevalence of ER was 56%, 34%, 61%, and 33% of, respectively, 30, 82, 29, and 30 screened relatives. In these families, transmission of an ER pattern is compatible with an autosomal dominant mode of inheritance. All probands were screened for genes identified in ERS, and no mutation was found. The Valsalva maneuver was performed in 80 relatives, resulting in increased J-wave amplitude for 17 of 20 affected patients and revealing an ER pattern in 17 relatives in whom 5 are obligate transmitters of an ER pattern.
sions