메뉴 건너뛰기




Volumn 72, Issue 4, 2008, Pages 592-597

Association of human SCN5A polymorphisms with idiopathic ventricular arrhythmia in a Chinese han cohort

Author keywords

Human cardiac sodium channel subunit gene; Idiopathic ventricular arrhythmia; Single nucleotide polymorphisms

Indexed keywords

ADULT; AGED; ARTICLE; AUTOANALYSIS; CHINESE; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HEART VENTRICLE ARRHYTHMIA; HUMAN; IDIOPATHIC DISEASE; MALE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; SCN5A GENE; SEQUENCE ANALYSIS; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 43549127283     PISSN: 13469843     EISSN: 13474820     Source Type: Journal    
DOI: 10.1253/circj.72.592     Document Type: Article
Times cited : (4)

References (29)
  • 1
    • 0033044972 scopus 로고    scopus 로고
    • Structure and function of the cardiac sodium channels
    • Balser JR. Structure and function of the cardiac sodium channels. Cardiovasc Res 1999; 42: 327-338.
    • (1999) Cardiovasc Res , vol.42 , pp. 327-338
    • Balser, J.R.1
  • 2
    • 0029992905 scopus 로고    scopus 로고
    • Genomic organization of the human SCN5A gene encoding the cardiac sodium channel
    • Wang Q, Li Z, Shen J, Keating MT. Genomic organization of the human SCN5A gene encoding the cardiac sodium channel. Genomics 1996; 34: 9-16.
    • (1996) Genomics , vol.34 , pp. 9-16
    • Wang, Q.1    Li, Z.2    Shen, J.3    Keating, M.T.4
  • 3
    • 0028905566 scopus 로고
    • SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
    • Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 1995; 80: 805-811.
    • (1995) Cell , vol.80 , pp. 805-811
    • Wang, Q.1    Shen, J.2    Splawski, I.3    Atkinson, D.4    Li, Z.5    Robinson, J.L.6
  • 4
    • 8644232427 scopus 로고    scopus 로고
    • Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome
    • Shin DJ, Jang Y, Park HY, Lee JE, Yang K, Kim E, et al. Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome. J Hum Genet 2004; 49: 573-578.
    • (2004) J Hum Genet , vol.49 , pp. 573-578
    • Shin, D.J.1    Jang, Y.2    Park, H.Y.3    Lee, J.E.4    Yang, K.5    Kim, E.6
  • 5
    • 0032546384 scopus 로고    scopus 로고
    • Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
    • Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 1998; 392: 293-295.
    • (1998) Nature , vol.392 , pp. 293-295
    • Chen, Q.1    Kirsch, G.E.2    Zhang, D.3    Brugada, R.4    Brugada, J.5    Brugada, P.6
  • 8
    • 0242317397 scopus 로고    scopus 로고
    • Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)
    • Benson DW, Wang DW, Dyment M, Knilans TK, Fish FA, Strieper MJ, et al. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A). J Clin Invest 2003; 112: 1019-1028.
    • (2003) J Clin Invest , vol.112 , pp. 1019-1028
    • Benson, D.W.1    Wang, D.W.2    Dyment, M.3    Knilans, T.K.4    Fish, F.A.5    Strieper, M.J.6
  • 9
    • 12544257550 scopus 로고    scopus 로고
    • Sodium channel mutations and susceptibility of heart failure and atrial fibrillation
    • Olson TM, Michels VV, Ballew JD, Reyna SP, Karst ML, Herron KI, et al. Sodium channel mutations and susceptibility of heart failure and atrial fibrillation. JAMA 2005; 293: 447-454.
    • (2005) JAMA , vol.293 , pp. 447-454
    • Olson, T.M.1    Michels, V.V.2    Ballew, J.D.3    Reyna, S.P.4    Karst, M.L.5    Herron, K.I.6
  • 10
    • 0037539913 scopus 로고    scopus 로고
    • L Veldkamp MW, Wilders R, Baartscheer A, Zegers JG, Bezzina CR, Wilde AAM. Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families. Circ Res 2003; 92: 976-983.
    • L Veldkamp MW, Wilders R, Baartscheer A, Zegers JG, Bezzina CR, Wilde AAM. Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families. Circ Res 2003; 92: 976-983.
  • 11
    • 21144469749 scopus 로고    scopus 로고
    • Link between SCN5A mutation and the Brugada Syndrome ECG phenotype: Simulation study
    • Miyoshi S, Mitamura H, Fukuda Y, Tanimoto K, Hagiwara Y, Kankai H, et al. Link between SCN5A mutation and the Brugada Syndrome ECG phenotype: Simulation study. Circ J 2005; 69: 567-575.
    • (2005) Circ J , vol.69 , pp. 567-575
    • Miyoshi, S.1    Mitamura, H.2    Fukuda, Y.3    Tanimoto, K.4    Hagiwara, Y.5    Kankai, H.6
  • 12
    • 3843095882 scopus 로고    scopus 로고
    • Genetic analysis of Brugada syndrome in Western Japan: Two novel mutations
    • Niimura H, Matsunaga A, Kumagai K, Ohwahi K, Ogawa M, Noguchi H, et al. Genetic analysis of Brugada syndrome in Western Japan: Two novel mutations. Circ J 2004; 68: 740-746.
    • (2004) Circ J , vol.68 , pp. 740-746
    • Niimura, H.1    Matsunaga, A.2    Kumagai, K.3    Ohwahi, K.4    Ogawa, M.5    Noguchi, H.6
  • 13
    • 0037314358 scopus 로고    scopus 로고
    • A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation
    • Viswanathan PC, Benson DW, Balser JR. A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation. J Clin Invest 2003; 111: 341-346.
    • (2003) J Clin Invest , vol.111 , pp. 341-346
    • Viswanathan, P.C.1    Benson, D.W.2    Balser, J.R.3
  • 14
    • 0037421629 scopus 로고    scopus 로고
    • A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation
    • Ye B, Valdivia CR, Ackerman MJ, Makielski JC. A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation. Physiol Genomics 2002; 12: 187-193.
    • (2002) Physiol Genomics , vol.12 , pp. 187-193
    • Ye, B.1    Valdivia, C.R.2    Ackerman, M.J.3    Makielski, J.C.4
  • 15
    • 33747146463 scopus 로고    scopus 로고
    • SCN5A Polymorphism Restores Trafficking of a Brugada Syndrome Mutation on a Separate Gene
    • Poelzing S, Forleo C, Samodell M, Dudash L, Sorrentino S, Anaclerio M, et al. SCN5A Polymorphism Restores Trafficking of a Brugada Syndrome Mutation on a Separate Gene. Circulation 2006; 114: 368-376.
    • (2006) Circulation , vol.114 , pp. 368-376
    • Poelzing, S.1    Forleo, C.2    Samodell, M.3    Dudash, L.4    Sorrentino, S.5    Anaclerio, M.6
  • 17
    • 13444300924 scopus 로고    scopus 로고
    • Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, et al. Brugada syndrome: Report of the second consensus conference: Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation 2005; 111: 659-670.
    • Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, et al. Brugada syndrome: Report of the second consensus conference: Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation 2005; 111: 659-670.
  • 19
    • 6944247406 scopus 로고    scopus 로고
    • Prevalence and electrocardiographic characteristics of idiopathic ventricular arrhythmia originating in the free wall of the right ventricular outflow tract
    • Tada H, Ito S, Naito S, Kurosaki K, Ueda M, Shinbo G, et al. Prevalence and electrocardiographic characteristics of idiopathic ventricular arrhythmia originating in the free wall of the right ventricular outflow tract. Circ J 2004; 68: 909-914.
    • (2004) Circ J , vol.68 , pp. 909-914
    • Tada, H.1    Ito, S.2    Naito, S.3    Kurosaki, K.4    Ueda, M.5    Shinbo, G.6
  • 20
    • 15744389143 scopus 로고    scopus 로고
    • Long-term course and clinical characteristics of ventricular tachycardia detected in children by school-based heart disease screening
    • Iwamoto M, Niimura I, Shibata T, Yasui K, Takigiku K, Nishizawa T, et al. Long-term course and clinical characteristics of ventricular tachycardia detected in children by school-based heart disease screening. Circ J 2005; 69: 273-276.
    • (2005) Circ J , vol.69 , pp. 273-276
    • Iwamoto, M.1    Niimura, I.2    Shibata, T.3    Yasui, K.4    Takigiku, K.5    Nishizawa, T.6
  • 21
    • 23844527207 scopus 로고    scopus 로고
    • Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks
    • Burke A, Creighton W, Mont E, Li L, Hogan S, Kutys R, et al. Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks. Circulation 2005; 112: 798-802.
    • (2005) Circulation , vol.112 , pp. 798-802
    • Burke, A.1    Creighton, W.2    Mont, E.3    Li, L.4    Hogan, S.5    Kutys, R.6
  • 22
    • 32444436881 scopus 로고    scopus 로고
    • A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y
    • Plant LD, Bowers PN, Liu Q, Morgan T, Zhang T, State MW, et al. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. J Clin Invest 2006; 116: 430-435.
    • (2006) J Clin Invest , vol.116 , pp. 430-435
    • Plant, L.D.1    Bowers, P.N.2    Liu, Q.3    Morgan, T.4    Zhang, T.5    State, M.W.6
  • 23
    • 0037161355 scopus 로고    scopus 로고
    • Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes
    • Yang P, Kanki H, Drolet B, Yang T, Wei J, Viswanathan PC, et al. Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes. Circulation 2002; 105: 1943-1948.
    • (2002) Circulation , vol.105 , pp. 1943-1948
    • Yang, P.1    Kanki, H.2    Drolet, B.3    Yang, T.4    Wei, J.5    Viswanathan, P.C.6
  • 24
    • 0037432504 scopus 로고    scopus 로고
    • Nucleotide changes in the translated region of SCN5A from Japanese patients with Brugada syndrome and control subjects
    • Takahata T, Yasui-Furukori N, Sasaki S, Igarashi T, Okumura K, Munakata A, et al. Nucleotide changes in the translated region of SCN5A from Japanese patients with Brugada syndrome and control subjects. Life Sci 2003; 72: 2391-2399.
    • (2003) Life Sci , vol.72 , pp. 2391-2399
    • Takahata, T.1    Yasui-Furukori, N.2    Sasaki, S.3    Igarashi, T.4    Okumura, K.5    Munakata, A.6
  • 25
    • 22244447116 scopus 로고    scopus 로고
    • Genetic polymorphisms and haplotypes of the human cardiac sodium channel α subunit gene (SCN5A) in Japanese and their association with arrhythmia
    • Maekawa K, Saito Y, Ozawa S, Adachi-Akahane S, Kawamoto M, Komamura K, et al. Genetic polymorphisms and haplotypes of the human cardiac sodium channel α subunit gene (SCN5A) in Japanese and their association with arrhythmia. Ann Hum Gene 2005; 69: 413-428.
    • (2005) Ann Hum Gene , vol.69 , pp. 413-428
    • Maekawa, K.1    Saito, Y.2    Ozawa, S.3    Adachi-Akahane, S.4    Kawamoto, M.5    Komamura, K.6
  • 26
    • 0032499656 scopus 로고    scopus 로고
    • Age- and sex-related differences in clinical manifestations in patients with congenital long-OT syndrome: Findings from the International LQTS Registry
    • Locati EH, Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Lehmann MH, et al. Age- and sex-related differences in clinical manifestations in patients with congenital long-OT syndrome: Findings from the International LQTS Registry. Circulation 1998; 97: 2237-2244.
    • (1998) Circulation , vol.97 , pp. 2237-2244
    • Locati, E.H.1    Zareba, W.2    Moss, A.J.3    Schwartz, P.J.4    Vincent, G.M.5    Lehmann, M.H.6
  • 27
    • 0031032133 scopus 로고    scopus 로고
    • Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome
    • Lehman MH, Timonthy KW, Frankovich D, Fromm BS, Keating M, Locati EH, et al. Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome. J Am Coll Cardiol 1997; 29: 93-99.
    • (1997) J Am Coll Cardiol , vol.29 , pp. 93-99
    • Lehman, M.H.1    Timonthy, K.W.2    Frankovich, D.3    Fromm, B.S.4    Keating, M.5    Locati, E.H.6
  • 28
    • 33947241926 scopus 로고    scopus 로고
    • Sex hormone and gender difference - role of testosterone on male predominance in Brugada syndrome
    • Shimizu W, Matsuo K, Kokubo Y, Satomi K, Kurita T, Noda T, et al. Sex hormone and gender difference - role of testosterone on male predominance in Brugada syndrome. J Cardiovasc. Electrophysiol. 2007; 18: 415-421.
    • (2007) J Cardiovasc. Electrophysiol , vol.18 , pp. 415-421
    • Shimizu, W.1    Matsuo, K.2    Kokubo, Y.3    Satomi, K.4    Kurita, T.5    Noda, T.6
  • 29
    • 33947204095 scopus 로고    scopus 로고
    • Gender differences in Brugada syndrome
    • Eckardt L. Gender differences in Brugada syndrome. J Cardiovasc Electrophysiol 2001; 18: 422-424.
    • (2001) J Cardiovasc Electrophysiol , vol.18 , pp. 422-424
    • Eckardt, L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.