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
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2018年 / 7卷 / 18期
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
  • [21] A Novel SCN5A Variant Causes Temperature-Sensitive Loss Of Function in a Family with Symptomatic Brugada Syndrome, Cardiac Conduction Disease, and Sick Sinus Syndrome
    Sanner, Karolina
    Mueller-Leisse, Johanna
    Zormpas, Christos
    Duncker, David
    Leffler, Andreas
    Veltmann, Christian
    [J]. CARDIOLOGY, 2021, 146 (06) : 754 - 762
  • [22] Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A
    Kodama, Takahide
    Serio, Alessandra
    Disertori, Marcello
    Bronzetti, Gabriele
    Diegoli, Marta
    Narula, Nupoor
    Grasso, Maurizia
    Mazzola, Silvia
    Arbustini, Eloisa
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2013, 167 (06) : 3078 - 3080
  • [23] SCN5A Mutation Is Associated With Early and Frequent Recurrence of Ventricular Fibrillation in Patients With Brugada Syndrome
    Nishii, Nobuhiro
    Ogawa, Masahiro
    Morita, Hiroshi
    Nakamura, Kazufumi
    Banba, Kimikazu
    Miura, Daiji
    Kumagai, Naoko
    Matsunaga, Akira
    Kawamura, Hiroshi
    Urakawa, Shigemi
    Miyaji, Kohei
    Nagai, Masahiro
    Satoh, Katsumasa
    Nakagawa, Koji
    Tanaka, Masamichi
    Hiramatsu, Shigeki
    Tada, Takeshi
    Murakami, Masato
    Nagase, Satoshi
    Kohno, Kunihisa
    Kusano, Kengo Fukushima
    Saku, Keijiro
    Ohe, Tohru
    Ito, Hiroshi
    [J]. CIRCULATION JOURNAL, 2010, 74 (12) : 2572 - 2578
  • [24] SCN5A compound heterozygosity mutation in Brugada syndrome: Functional consequences and the implication for pharmacological treatment
    Joviano-Santos, J., V
    Santos-Miranda, A.
    Neri, E. A.
    Fonseca-Alaniz, M. H.
    Krieger, J. E.
    Pereira, A. C.
    Roman-Campos, D.
    [J]. LIFE SCIENCES, 2021, 278
  • [25] Progressive cardiac conduction defect is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation
    Probst, V
    Allouis, M
    Sacher, F
    Pattier, S
    Babuty, D
    Mabo, P
    Mansourati, J
    Victor, J
    Nguyen, JM
    Schott, JJ
    Boisseau, P
    Escande, D
    Le Marec, H
    [J]. JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2006, 17 (03) : 270 - 275
  • [26] In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant
    Doisne, Nicolas
    Grauso, Marta
    Mougenot, Nathalie
    Clergue, Michel
    Souil, Charlotte
    Coulombe, Alain
    Guicheney, Pascale
    Neyroud, Nathalie
    [J]. FRONTIERS IN PHYSIOLOGY, 2021, 12
  • [27] Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities
    Frigo, Gianfranco
    Rampazzo, Alessandra
    Bauce, Barbara
    Pilichou, Kalliopi
    Beffagna, Giorgia
    Danieli, Gian Antonio
    Nava, Andrea
    Martini, Bortolo
    [J]. EUROPACE, 2007, 9 (06): : 391 - 397
  • [28] Novel SCN5A mutation associated with idiopathic ventricular fibrillation due to subclinical Brugada syndrome
    Jimenez-Jaimez, Juan
    Alvarez-Lopez, Miguel
    Tercedor-Sanchez, Luis
    Santiago, Pablo
    Algarra, Maria
    Penas, Rocio
    Valverde, Francisca
    Melgares-Moreno, Rafael
    [J]. CARDIOGENETICS, 2012, 2 (01) : 1 - 5
  • [29] Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A
    Zhu, Yao-Bin
    Zhang, Jian-Hui
    Ji, Yuan-Yuan
    Hu, Ya-Nan
    Wang, Han-Lu
    Ruan, Dan-Dan
    Meng, Xiao-Rong
    Lin, Xin-Fu
    Luo, Jie-Wei
    Chen, Wei
    [J]. CARDIOLOGY RESEARCH AND PRACTICE, 2022, 2022
  • [30] SCN5A variants in Brugada syndrome: True, true false, or false true
    Walsh, Roddy
    Wilde, Arthur A. M.
    [J]. JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2019, 30 (01) : 128 - 131