Clinical aspects and prognosis of Brugada syndrome in children

Circulation

Volumn 115, Issue 15, 2007, Pages 2042-2048

  Probst, Vincent ^a,b,c,p   Denjoy, Isabelle ^d   Meregalli, Paola G ^e   Amirault, Jean Christophe ^a,c   Sacher, Fréderic ^f   Mansourati, Jacques ^g   Babuty, Dominique ^h   Villain, Elisabeth ⁱ   Victor, Jacques ^j   Schott, Jean Jacques ^b   Lupoglazoff, Jean Marc ^k   Mabo, Philippe ^l   Veltmann, Christian ^m   Jesel, Laurence ⁿ   Chevalier, Philippe ^o   Clur, Sally Ann B ^e   Haissaguerre, Michel ^f   Wolpert, Christian ^m   Le Marec, Hervé ^a,b,c   Wilde, Arthur A M ^e  

^a NANTES UNIVERSITY HOSPITAL   (France)

^b INSERM   (France)

^c CIC Nantes   (France)

^d Lariboisiere Hospital   (France)

^e UNIVERSITY OF AMSTERDAM   (Netherlands)

^f HAUT LÉVÊQUE HOSPITAL   (France)

^g BREST UNIVERSITY HOSPITAL   (France)

^h SERVICE DE DERMATOLOGIE   (France)

ⁱ HÔPITAL NECKER ENFANTS MALADES   (France)

^j ANGERS UNIVERSITY HOSPITAL   (France)

^k HÔPITAL ROBERT DEBRÉ   (France)

^l PONTCHAILLOU UNIVERSITY HOSPITAL   (France)

^m UNIVERSITY OF HEIDELBERG   (Germany)

ⁿ UNIVERSITY HOSPITAL OF STRASBOURG   (France)

^o HOSPICES CIVILS DE LYON   (France)

^p CHU de Nantes   (France)

more..

Author keywords

Arrhythmia; Brugada syndrome; Death, sudden; Genetics; Ion channels; Pediatrics; Tachyarrhythmias

Indexed keywords

DIHYDROQUINIDINE;

ADOLESCENT; ARTICLE; BRUGADA SYNDROME; CARDIAC PATIENT; CARDIOVASCULAR RISK; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DEFIBRILLATOR; ELECTROCARDIOGRAM; FAMILY; FEMALE; FEVER; FOLLOW UP; HEART ARRHYTHMIA; HUMAN; IMPLANT; MALE; PRIORITY JOURNAL; PROGNOSIS; RISK FACTOR; SHOCK; SINUS NODE; SUDDEN DEATH; SUPRAVENTRICULAR TACHYCARDIA; SYMPTOMATOLOGY; SYNCOPE;

ADOLESCENT; ANTI-ARRHYTHMIA AGENTS; BRUGADA SYNDROME; CHILD; CHILD, PRESCHOOL; DEATH, SUDDEN, CARDIAC; DEFIBRILLATORS, IMPLANTABLE; ELECTROCARDIOGRAPHY; FEMALE; FOLLOW-UP STUDIES; GENES, DOMINANT; HUMANS; INFANT; MALE; MUSCLE PROTEINS; PROGNOSIS; QUINIDINE; SODIUM CHANNEL BLOCKERS; SODIUM CHANNELS; SYNCOPE; TACHYCARDIA, SUPRAVENTRICULAR;

EID: 34247212362     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/CIRCULATIONAHA.106.664219     Document Type: Article

References (35)

1. Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome: a multicenter report. J Am Coll Cardiol. 1992;20:1391-1396.
2. Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, Potenza D, Moya A, Borggrefe M, Breithardt G, Ortiz-Lopez R, Wang Z, Antzelevitch C, O'Brien RE, Schulze-Bahr E, Keating MT, Towbin JA, Wang Q. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature. 1998;392:293-296.
3. Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, Gussak I, LeMarec H, Nademanee K, Perez Riera AR, Shimizu W, Schulze-Bahr E, Tan H, Wilde A. Brugada syndrome: report of the Second Consensus Conference. Heart Rhythm. 2005;2:429-440.
4. Wilde AA, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RN, Kass RS, Nademanee K, Priori SG, Towbin JA. Proposed diagnostic criteria for the Brugada syndrome: consensus report. Circulation. 2002;106:2514-2519.
5. Gehi AK, Duong TD, Metz LD, Gomes JA, Mehta D. Risk stratification of individuals with the Brugada electrocardiogram: a meta-analysis. J Cardiovasc Electrophysiol. 2006;17:577-583.
6. Eckardt L, Probst V, Smits JP, Bahr ES, Wolpert C, Schimpf R, Wichter T, Boisseau P, Heinecke A, Breithardt G, Borggrefe M, LeMarec H, Bocker D, Wilde AA. Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome. Circulation. 2005;111:257-263.
7. Priori SG, Napolitano C, Gasparini M, Pappone C, Della Bella P, Giordano U, Bloise R, Giustetto C, De Nardis R, Grillo M, Ronchetti E, Faggiano G, Nastoli J. Natural history of Brugada syndrome: insights for risk stratification and management. Circulation. 2002;105:1342-1347.
8. Brugada P, Geelen P, Brugada R, Mont L, Brugada J. Prognostic value of electrophysiologic investigations in Brugada syndrome. J Cardiovasc Electrophysiol. 2001;12:1004-1007.
9. Skinner JR, Chung S-K, Montgomery D, McCulley CH, Crawford J, French J, Rees MI. Near-miss SIDS due to Brugada syndrome. Arch Dis Child. 2005;90:528-529.
10. Suzuki H, Torigoe K, Numata O, Yazaki S. Infant case with a malignant form of Brugada syndrome. J Cardiovasc Electrophysiol. 2000;11:1277-1280.
11. 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.
12. Wren C, O'Sullivan JJ, Wright C. Sudden death in children and adolescents. Heart. 2000;83:410-413.
13. Yamakawa Y, Ishikawa T, Uchino K, Mochida Y, Ebina T, Sumita S, Kobayashi T, Matsushita K, Matsumoto K, Ohkusu Y, Nishizawa T, Takigiku K, Iwamoto M, Kimura K, Umemura S. Prevalence of right bundle-branch block and right precordial ST-segment elevation (Brugada-type electrocardiogram) in Japanese children. Circ J. 2004;68:275-279.
14. Miyasaka Y, Tsuji H, Yamada K, Tokunaga S, Saito D, Imuro Y, Matsumoto N, Iwasaka T. Prevalence and mortality of the Brugada-type electrocardiogram in one city in Japan. J Am Coll Cardiol. 2001;38:771-774.
15. Hermida JS, Lemoine JL, Aoun FB, Jarry G, Rey JL, Quiret JC. Prevalence of the Brugada syndrome in an apparently healthy population. Am J Cardiol. 2000;86:91-94.
16. Probst V, Evain S, Gournay V, Marie A, Schott JJ, Boisseau P, Le Marec H. Monomorphic ventricular tachycardia due to Brugada syndrome successfully treated by hydroquinidine therapy in a 3-year-old child. J Cardiovasc Electrophysiol. 2006;17:97-100.
17. Priori SG, Napolitano C, Giordano U, Collisani G, Memmi M. Brugada syndrome and sudden cardiac death in children. Lancet. 2000;355:808-809.
18. Sanatani S, Mahkseed N, Vallance H, Brugada R. The Brugada ECG pattern in a neonate. J Cardiovasc Electrophysiol. 2005;16:342-344.
19. Sreeram N, Simmers T, Brockmeier K. The Brugada syndrome: its relevance to paediatric practice. Z Kardiol. 2004;93:784-790.
20. Beaufort-Krol GC, van den Berg MP, Wilde AA, van Tintelen JP, Viersma JW, Bezzina CR, Bink-Boelkens MT. Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood. J Am Coll Cardiol. 2005;46:331-337.
21. Matsuo K, Akahoshi M, Seto S, Yano K. Disappearance of the Brugada-type electrocardiogram after surgical castration: a role for testosterone and an explanation for the male preponderance. Pacing Clin Electrophysiol. 2003;26:1551-1553.
22. Forest MG, De Peretti E, Bertrand J. Hypothalamic-pituitary-gonadal relationships in man from birth to puberty. Clin Endocrinol (Oxf). 1976;5:551-569.
23. Antzelevitch C, Brugada P, Brugada J, Brugada R, Shimizu W, Gussak I, Perez Riera AR. Brugada syndrome: a decade of progress. Circ Res. 2002;91:1114-1118.
24. Dumaine R, Towbin JA, Brugada P, Vatta M, Nesterenko DV, Nesterenko VV, Brugada J, Brugada R, Antzelevitch C. Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent. Circ Res. 1999;85:803-809.
25. Keller DI, Rougier JS, Kucera JP, Benammar N, Fressart V, Guicheney P, Madle A, Fromer M, Schlapfer J, Abriel H. Brugada syndrome and fever: genetic and molecular characterization of patients carrying SCN5A mutations. Cardiovasc Res. 2005;67:510-519.
26. Pasquie JL, Sanders P, Hocini M, Hsu LF, Scavee C, Jais P, Takahashi Y, Rotter M, Sacher F, Victor J, Clementy J, Haissaguerre M. Fever as a precipitant of idiopathic ventricular fibrillation in patients with normal hearts. J Cardiovasc Electrophysiol. 2004;15:1271-1276.
27. Eckardt L, Kirchhof P, Loh P, Schulze-Bahr E, Johna R, Wichter T, Breithardt G, Haverkamp W, Borggrefe M. Brugada syndrome and supraventricular tachyarrhythmias: a novel association? J Cardiovasc Electrophysiol. 2001;12:680-685.
28. Gillette PC. The mechanisms of supraventricular tachycardia in children. Circulation. 1976;54:133-139.
29. Benson DW, Wang DW, Dyment M, Knilans TK, Fish FA, Strieper MJ, Rhodes TH, George AL Jr. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A). J Clin Invest. 2003;112:1019-1028.
30. Rossenbacker T, Carroll SJ, Liu H, Kuiperi C, de Ravel TJ, Devriendt K, Carmeliet P, Kass RS, Heidbuchel H. Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death. Heart Rhythm. 2004;1:610-615.
31. Smits JP, Koopmann TT, Wilders R, Veldkamp MW, Opthof T, Bhuiyan ZA, Mannens MM, Balser JR, Tan HL, Bezzina CR, Wilde AA. A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families. J Mol Cell Cardiol. 2005;38:969-981.
32. + current in pacemaker cells isolated from rabbit sinoatrial node. Am J Physiol. 1996;270:H2108-H2119.
33. Lei M, Goddard C, Liu J, Leoni AL, Royer A, Fung SS, Xiao G, Ma A, Zhang H, Charpentier F, Vandenberg JI, Colledge WH, Grace AA, Huang CL. Sinus node dysfunction following targeted disruption of the murine cardiac sodium channel gene Scn5a. J Physiol. 2005;567:387-400.
34. Hermida JS, Denjoy I, Clerc J, Extramiana F, Jarry G, Milliez P, Guicheney P, Di Fusco S, Rey JL, Cauchemez B, Leenhardt A. Hydroquinidine therapy in Brugada syndrome. J Am Coll Cardiol. 2004;43:1853-1860.
35. Belhassen B, Glick A, Viskin S. Efficacy of quinidine in high-risk patients with Brugada syndrome. Circulation. 2004;110:1731-1737.