Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome

被引:13
|
作者
Aizawa, Yoshiyasu [1 ]
Fujisawa, Taishi [1 ]
Katsumata, Yoshinori [1 ,6 ]
Kohsaka, Shun [1 ]
Kunitomi, Akira [1 ]
Ohno, Seiko [2 ,3 ]
Sonoda, Keiko [2 ,3 ]
Hayashi, Hidemori [4 ]
Hojo, Rintaro [5 ]
Fukamizu, Seiji [5 ]
Nagase, Satoshi [3 ]
Ito, Shogo [1 ]
Nakajima, Kazuaki [1 ]
Nishiyama, Takahiko [1 ]
Kimura, Takehiro [1 ]
Kurita, Yasuo
Furukawa, Yoshiko [6 ]
Takatsuki, Seiji [1 ]
Ogawa, Satoshi [6 ]
Nakazato, Yuji [4 ]
Sumiyoshi, Masataka [4 ]
Kosaki, Kenjiro [1 ]
Horie, Minoru [2 ]
Fukuda, Keiichi [1 ]
机构
[1] Keio Univ Hosp, Tokyo, Japan
[2] Shiga Univ Med Sci, Otsu, Shiga, Japan
[3] Natl Cerebral & Cardiovasc Ctr, Suita, Osaka, Japan
[4] Juntendo Univ, Tokyo, Japan
[5] Tokyo Metropolitan Hiroo Gen Hosp, Tokyo, Japan
[6] Int Univ Hlth & Welf, Tokyo, Japan
来源
关键词
Brugada syndrome; SCN5A; sex; sick sinus syndrome; PACEMAKER IMPLANTATION; GENDER-DIFFERENCES; PREDOMINANCE; DISEASE;
D O I
10.1161/JAHA.118.009387
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Brugada syndrome (BS) is known to be 9 times more prevalent in males than females. However, little is known about the development of sick sinus syndrome in female members with familial BS. Methods and Results-Familial BS patients and family members, both from our institutions and collaborating sites that specialize in clinical care of BS, participated in this study. We collected information on their clinical and genetic background, along with the inheritance patterns of BS. Detailed information on each case with familial BS is described. A total of 7 families, including 25 BS patients (12 females and 13 males), were included. Seven were probands and 18 were family members. Ten out of the 12 female patients and none of the 13 male patients developed sick sinus syndrome. Sudden death or spontaneous ventricular fibrillation occurred in 7 out of 13 male patients and 2 out of 12 female patients. Conclusions-Familial BS existed in which female patients developed sick sinus syndrome but male patients did not. Some of those female patients with sick sinus syndrome had unrecognized BS. Information should be collected not only regarding a family history of sudden death or BS, but also whether a pacemaker was implanted in female members.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] A new SCN5A mutation associate Brugada syndrome and sinus node dysfunction
    Kyndt, F
    Schott, JJ
    Probst, V
    Chevallier, JC
    Le Marec, H
    JOURNAL OF MOLECULAR MEDICINE-JMM, 2000, 78 (03): : B13 - B13
  • [2] Severe Atrial Dysfunction and Sick Sinus Syndrome in a Patient With Scn5a Mutation
    Font, Cristina
    Ho, Tiffany
    Torbey, Estelle
    CIRCULATION, 2022, 146
  • [3] SCN5A polymorphism rescues Brugada syndrome mutation
    Poelzing, S
    Sorrentino, S
    Anaclerio, M
    Troccoli, R
    Iacoviello, M
    Romito, R
    Guida, P
    Samodell, M
    Deschenes, I
    Pitzalis, M
    CIRCULATION, 2004, 110 (17) : 229 - 229
  • [4] A new SCN5A mutation associates Brugada syndrome and sinus node dysfunction.
    Kyndt, F
    Schott, JJ
    Probst, V
    Chevallier, JC
    Le Marec, H
    CIRCULATION, 2000, 102 (18) : 281 - 281
  • [5] Genetic factors conferring congenital sick sinus syndrome in SCN5A mutation carriers
    Makita, Naomasa
    Yamamoto, Hirokazu
    Sasaki, Koji
    Yokoshiki, Hisashi
    Motomura, Hideki
    Tsutsui, Hiroyuki
    CIRCULATION, 2006, 114 (18) : 505 - 505
  • [6] A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation
    Ziyadeh-Isleem, Azza
    Clatot, Jerome
    Duchatelet, Sabine
    Gandjbakhch, Estelle
    Denjoy, Isabelle
    Hidden-Lucet, Francoise
    Hatem, Stephane
    Deschenes, Isabelle
    Coulombe, Alain
    Neyroud, Nathalie
    Guicheney, Pascale
    HEART RHYTHM, 2014, 11 (06) : 1015 - 1023
  • [7] A novel mutation in the SCN5A gene is associated with Brugada syndrome
    Shin, Dong-Jik
    Kim, Eunmin
    Park, Sang-Bum
    Jang, Won-Cheoul
    Bae, Yoonsun
    Han, Jihye
    Jang, Yangsoo
    Joung, Boyoung
    Lee, Moon Hyoung
    Kim, Sung Soon
    Huang, Hai
    Chahine, Mohamed
    Yoon, Sungjoo Kim
    LIFE SCIENCES, 2007, 80 (08) : 716 - 724
  • [8] SUDS and Brugada syndrome linked by the same SCN5A mutation
    Hong, K
    Vatta, M
    Poungvarin, N
    Oliva, A
    Berruero, A
    Pinero, C
    Brugada, J
    Brugada, P
    Towbin, JA
    Dumaine, R
    Antzelevitch, C
    Brugada, R
    CIRCULATION, 2002, 106 (19) : 61 - 61
  • [9] Double SCN5A mutation underlying asymptomatic Brugada syndrome
    Yokoi, H
    Makita, N
    Sasaki, K
    Takagi, Y
    Okumura, Y
    Nishino, T
    Makiyama, T
    Kitabatake, A
    Horie, M
    Watanabe, I
    Tsutsui, H
    HEART RHYTHM, 2005, 2 (03) : 285 - 292
  • [10] Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation
    Parisi, Pasquale
    Oliva, Antonio
    Coll Vida, Monica
    Partemi, Sara
    Campuzano, Oscar
    Iglesias, Anna
    Pisani, Daniela
    Pascali, Vincenzo L.
    Paolino, Maria Chiara
    Villa, Maria Pia
    Zara, Federico
    Tassinari, Carlo Alberto
    Striano, Pasquale
    Brugada, Ramon
    EPILEPSY RESEARCH, 2013, 105 (03) : 415 - 418