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Volumn 6, Issue 11, 2009, Pages 1652-1659

Catecholaminergic polymorphic ventricular tachycardia: A paradigm to understand mechanisms of arrhythmias associated to impaired Ca2+ regulation

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; CALCIUM CHANNEL; CATECHOLAMINE;

EID: 70350505897     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2009.06.033     Document Type: Article
Times cited : (84)

References (41)
  • 1
    • 0028957403 scopus 로고
    • Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients
    • Leenhardt A., Lucet V., Denjoy I., Grau F., Ngoc D.D., and Coumel P. Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients. Circulation 91 (1995) 1512-1519
    • (1995) Circulation , vol.91 , pp. 1512-1519
    • Leenhardt, A.1    Lucet, V.2    Denjoy, I.3    Grau, F.4    Ngoc, D.D.5    Coumel, P.6
  • 2
    • 0001276591 scopus 로고
    • Catecholamine-induced severe ventricular arrhythmias with Adam-Stokes in children: report of four cases
    • Coumel P., Fidelle J., Lucet V., Attuel P., and Bouvrain Y. Catecholamine-induced severe ventricular arrhythmias with Adam-Stokes in children: report of four cases. Br Heart J 40 Suppl (1978) 28-37
    • (1978) Br Heart J , vol.40 , Issue.SUPPL , pp. 28-37
    • Coumel, P.1    Fidelle, J.2    Lucet, V.3    Attuel, P.4    Bouvrain, Y.5
  • 3
    • 0035895322 scopus 로고    scopus 로고
    • Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
    • Priori S.G., Napolitano C., Tiso N., et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 103 (2001) 196-200
    • (2001) Circulation , vol.103 , pp. 196-200
    • Priori, S.G.1    Napolitano, C.2    Tiso, N.3
  • 4
    • 0035205336 scopus 로고    scopus 로고
    • A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
    • Lahat H., Pras E., Olender T., et al. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. Am J Hum Genet 69 (2001) 1378-1384
    • (2001) Am J Hum Genet , vol.69 , pp. 1378-1384
    • Lahat, H.1    Pras, E.2    Olender, T.3
  • 5
    • 0036645605 scopus 로고    scopus 로고
    • Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia
    • Priori S.G., Napolitano C., Memmi M., et al. Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. Circulation 106 (2002) 69-74
    • (2002) Circulation , vol.106 , pp. 69-74
    • Priori, S.G.1    Napolitano, C.2    Memmi, M.3
  • 6
    • 33645170442 scopus 로고    scopus 로고
    • Clinical and molecular characterization of a large cohort of patients affected with catecholaminergic polymorphic ventricular tachycardia
    • Cerrone M., Colombi B., Bloise R., et al. Clinical and molecular characterization of a large cohort of patients affected with catecholaminergic polymorphic ventricular tachycardia. Circulation 110 Suppl (2004) 552
    • (2004) Circulation , vol.110 , Issue.SUPPL , pp. 552
    • Cerrone, M.1    Colombi, B.2    Bloise, R.3
  • 7
    • 47049122897 scopus 로고    scopus 로고
    • Electrocardiographic analysis of arrhythmias developing during exercise in patients with catecholaminergic polymorphic ventricular tachycardia
    • Monteforte N., Raytcheva-Buono E., Bloise R., et al. Electrocardiographic analysis of arrhythmias developing during exercise in patients with catecholaminergic polymorphic ventricular tachycardia. Circulation 116 (2007) 492
    • (2007) Circulation , vol.116 , pp. 492
    • Monteforte, N.1    Raytcheva-Buono, E.2    Bloise, R.3
  • 8
    • 34948816746 scopus 로고    scopus 로고
    • Association of atrial arrhythmia and sinus node dysfunction in patients with catecholaminergic polymorphic ventricular tachycardia
    • Sumitomo N., Sakurada H., Taniguchi K., et al. Association of atrial arrhythmia and sinus node dysfunction in patients with catecholaminergic polymorphic ventricular tachycardia. Circ J 71 (2007) 1606-1609
    • (2007) Circ J , vol.71 , pp. 1606-1609
    • Sumitomo, N.1    Sakurada, H.2    Taniguchi, K.3
  • 9
    • 0033405388 scopus 로고    scopus 로고
    • Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
    • Swan H., Piippo K., Viitasalo M., et al. Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts. J Am Coll Cardiol 34 (1999) 2035-2042
    • (1999) J Am Coll Cardiol , vol.34 , pp. 2035-2042
    • Swan, H.1    Piippo, K.2    Viitasalo, M.3
  • 10
    • 33745492545 scopus 로고    scopus 로고
    • Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testing
    • Tester D.J., Arya P., Will M., et al. Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testing. Heart Rhythm 3 (2006) 800-805
    • (2006) Heart Rhythm , vol.3 , pp. 800-805
    • Tester, D.J.1    Arya, P.2    Will, M.3
  • 11
    • 33748512585 scopus 로고    scopus 로고
    • Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia
    • di Barletta M.R., Viatchenko-Karpinski S., Nori A., et al. Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia. Circulation 114 (2006) 1012-1019
    • (2006) Circulation , vol.114 , pp. 1012-1019
    • di Barletta, M.R.1    Viatchenko-Karpinski, S.2    Nori, A.3
  • 12
    • 34548660764 scopus 로고    scopus 로고
    • A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22
    • Bhuiyan Z.A., Hamdan M.A., Shamsi E.T., et al. A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22. J Cardiovasc Electrophysiol 18 (2007) 1060-1066
    • (2007) J Cardiovasc Electrophysiol , vol.18 , pp. 1060-1066
    • Bhuiyan, Z.A.1    Hamdan, M.A.2    Shamsi, E.T.3
  • 13
    • 20344400985 scopus 로고    scopus 로고
    • Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor
    • Cerrone M., Colombi B., Santoro M., et al. Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor. Circ Res 96 (2005) e77-e82
    • (2005) Circ Res , vol.96
    • Cerrone, M.1    Colombi, B.2    Santoro, M.3
  • 14
    • 33747072861 scopus 로고    scopus 로고
    • Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy
    • Kannankeril P.J., Mitchell B.M., Goonasekera S.A., et al. Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy. Proc Natl Acad Sci U S A 103 (2006) 12179-12184
    • (2006) Proc Natl Acad Sci U S A , vol.103 , pp. 12179-12184
    • Kannankeril, P.J.1    Mitchell, B.M.2    Goonasekera, S.A.3
  • 15
    • 45749100010 scopus 로고    scopus 로고
    • Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice
    • Lehnart S.E., Mongillo M., Bellinger A., et al. Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice. J Clin Invest 118 (2008) 2230-2245
    • (2008) J Clin Invest , vol.118 , pp. 2230-2245
    • Lehnart, S.E.1    Mongillo, M.2    Bellinger, A.3
  • 16
    • 33748292955 scopus 로고    scopus 로고
    • Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia
    • Knollmann B.C., Chopra N., Hlaing T., et al. Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia. J Clin Invest 116 (2006) 2510-2520
    • (2006) J Clin Invest , vol.116 , pp. 2510-2520
    • Knollmann, B.C.1    Chopra, N.2    Hlaing, T.3
  • 17
    • 34447133403 scopus 로고    scopus 로고
    • Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia
    • Song L., Alcalai R., Arad M., et al. Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia. J Clin Invest 117 (2007) 1814-1823
    • (2007) J Clin Invest , vol.117 , pp. 1814-1823
    • Song, L.1    Alcalai, R.2    Arad, M.3
  • 18
    • 33746788063 scopus 로고    scopus 로고
    • Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model
    • Liu N., Colombi B., Memmi M., et al. Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model. Circ Res 99 (2006) 292-298
    • (2006) Circ Res , vol.99 , pp. 292-298
    • Liu, N.1    Colombi, B.2    Memmi, M.3
  • 19
    • 36048938672 scopus 로고    scopus 로고
    • Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia
    • Cerrone M., Noujaim S.F., Tolkacheva E.G., et al. Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia. Circ Res 101 (2007) 1039-1048
    • (2007) Circ Res , vol.101 , pp. 1039-1048
    • Cerrone, M.1    Noujaim, S.F.2    Tolkacheva, E.G.3
  • 20
    • 34548317099 scopus 로고    scopus 로고
    • Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves
    • Paavola J., Viitasalo M., Laitinen-Forsblom P.J., et al. Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves. Eur Heart J 28 (2007) 1135-1142
    • (2007) Eur Heart J , vol.28 , pp. 1135-1142
    • Paavola, J.1    Viitasalo, M.2    Laitinen-Forsblom, P.J.3
  • 21
    • 0037047646 scopus 로고    scopus 로고
    • Enhanced basal activity of a cardiac Ca2+ release channel (ryanodine receptor) mutant associated with ventricular tachycardia and sudden death
    • Jiang D., Xiao B., Zhang L., and Chen S.R. Enhanced basal activity of a cardiac Ca2+ release channel (ryanodine receptor) mutant associated with ventricular tachycardia and sudden death. Circ Res 91 (2002) 218-225
    • (2002) Circ Res , vol.91 , pp. 218-225
    • Jiang, D.1    Xiao, B.2    Zhang, L.3    Chen, S.R.4
  • 22
    • 4444357245 scopus 로고    scopus 로고
    • RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR)
    • Jiang D., Xiao B., Yang D., et al. RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR). Proc Natl Acad Sci U S A 101 (2004) 13062-13067
    • (2004) Proc Natl Acad Sci U S A , vol.101 , pp. 13062-13067
    • Jiang, D.1    Xiao, B.2    Yang, D.3
  • 23
    • 33644673205 scopus 로고    scopus 로고
    • Enhanced store overload-induced Ca2+ release and channel sensitivity to luminal Ca2+ activation are common defects of RyR2 mutations linked to ventricular tachycardia and sudden death
    • Jiang D., Wang R., Xiao B., et al. Enhanced store overload-induced Ca2+ release and channel sensitivity to luminal Ca2+ activation are common defects of RyR2 mutations linked to ventricular tachycardia and sudden death. Circ Res 97 (2005) 1173-1181
    • (2005) Circ Res , vol.97 , pp. 1173-1181
    • Jiang, D.1    Wang, R.2    Xiao, B.3
  • 24
    • 59849125934 scopus 로고    scopus 로고
    • Increased Ca2+ sensitivity of the ryanodine receptor mutant RyR2R4496C underlies catecholaminergic polymorphic ventricular tachycardia
    • Fernandez-Velasco M., Rueda A., Rizzi N., et al. Increased Ca2+ sensitivity of the ryanodine receptor mutant RyR2R4496C underlies catecholaminergic polymorphic ventricular tachycardia. Circ Res 104 (2009) 201-209
    • (2009) Circ Res , vol.104 , pp. 201-209
    • Fernandez-Velasco, M.1    Rueda, A.2    Rizzi, N.3
  • 25
    • 0036514152 scopus 로고    scopus 로고
    • Regulation of calcium release by interdomain interaction within ryanodine receptors
    • Ikemoto N., and Yamamoto T. Regulation of calcium release by interdomain interaction within ryanodine receptors. Front Biosci 7 (2002) d671-d683
    • (2002) Front Biosci , vol.7
    • Ikemoto, N.1    Yamamoto, T.2
  • 26
    • 21544451389 scopus 로고    scopus 로고
    • Defective regulation of interdomain interactions within the ryanodine receptor plays a key role in the pathogenesis of heart failure
    • Oda T., Yano M., Yamamoto T., et al. Defective regulation of interdomain interactions within the ryanodine receptor plays a key role in the pathogenesis of heart failure. Circulation 111 (2005) 3400-3410
    • (2005) Circulation , vol.111 , pp. 3400-3410
    • Oda, T.1    Yano, M.2    Yamamoto, T.3
  • 27
    • 33644837101 scopus 로고    scopus 로고
    • Arrhythmogenic mutation-linked defects in ryanodine receptor autoregulation reveal a novel mechanism of Ca2+ release channel dysfunction
    • George C.H., Jundi H., Walters N., Thomas N.L., West R.R., and Lai F.A. Arrhythmogenic mutation-linked defects in ryanodine receptor autoregulation reveal a novel mechanism of Ca2+ release channel dysfunction. Circ Res 98 (2006) 88-97
    • (2006) Circ Res , vol.98 , pp. 88-97
    • George, C.H.1    Jundi, H.2    Walters, N.3    Thomas, N.L.4    West, R.R.5    Lai, F.A.6
  • 28
    • 0034640113 scopus 로고    scopus 로고
    • PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts
    • Marx S.O., Reiken S., Hisamatsu Y., et al. PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts. Cell 101 (2000) 365-376
    • (2000) Cell , vol.101 , pp. 365-376
    • Marx, S.O.1    Reiken, S.2    Hisamatsu, Y.3
  • 29
    • 1842482414 scopus 로고    scopus 로고
    • Protection from cardiac arrhythmia through ryanodine receptor-stabilizing protein calstabin2
    • Wehrens X.H., Lehnart S.E., Reiken S.R., et al. Protection from cardiac arrhythmia through ryanodine receptor-stabilizing protein calstabin2. Science 304 (2004) 292-296
    • (2004) Science , vol.304 , pp. 292-296
    • Wehrens, X.H.1    Lehnart, S.E.2    Reiken, S.R.3
  • 30
    • 0141571322 scopus 로고    scopus 로고
    • Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes
    • George C.H., Higgs G.V., and Lai F.A. Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes. Circ Res 93 (2003) 531-540
    • (2003) Circ Res , vol.93 , pp. 531-540
    • George, C.H.1    Higgs, G.V.2    Lai, F.A.3
  • 31
    • 34250772834 scopus 로고    scopus 로고
    • K201 (JTV519) suppresses spontaneous Ca2+ release and [3H]ryanodine binding to RyR2 irrespective of FKBP12.6 association
    • Hunt D.J., Jones P.P., Wang R., et al. K201 (JTV519) suppresses spontaneous Ca2+ release and [3H]ryanodine binding to RyR2 irrespective of FKBP12.6 association. Biochem J 404 (2007) 431-438
    • (2007) Biochem J , vol.404 , pp. 431-438
    • Hunt, D.J.1    Jones, P.P.2    Wang, R.3
  • 32
    • 34848900444 scopus 로고    scopus 로고
    • Characterization of human cardiac calsequestrin and its deleterious mutants
    • Kim E., Youn B., Kemper L., et al. Characterization of human cardiac calsequestrin and its deleterious mutants. J Mol Biol 373 (2007) 1047-1057
    • (2007) J Mol Biol , vol.373 , pp. 1047-1057
    • Kim, E.1    Youn, B.2    Kemper, L.3
  • 33
    • 33745032863 scopus 로고    scopus 로고
    • Abnormal interactions of calsequestrin with the ryanodine receptor calcium release channel complex linked to exercise-induced sudden cardiac death
    • Terentyev D., Nori A., Santoro M., et al. Abnormal interactions of calsequestrin with the ryanodine receptor calcium release channel complex linked to exercise-induced sudden cardiac death. Circ Res 98 (2006) 1151-1158
    • (2006) Circ Res , vol.98 , pp. 1151-1158
    • Terentyev, D.1    Nori, A.2    Santoro, M.3
  • 34
    • 53549118870 scopus 로고    scopus 로고
    • Unexpected structural and functional consequences of the R33Q homozygous mutation in cardiac calsequestrin: a complex arrhythmogenic cascade in a knock in mouse model
    • Rizzi N., Liu N., Napolitano C., et al. Unexpected structural and functional consequences of the R33Q homozygous mutation in cardiac calsequestrin: a complex arrhythmogenic cascade in a knock in mouse model. Circ Res 103 (2008) 298-306
    • (2008) Circ Res , vol.103 , pp. 298-306
    • Rizzi, N.1    Liu, N.2    Napolitano, C.3
  • 35
    • 66549094345 scopus 로고    scopus 로고
    • Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia
    • Hayashi M., Denjoy I., Extramiana F., et al. Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia. Circulation 119 (2009) 2426-2434
    • (2009) Circulation , vol.119 , pp. 2426-2434
    • Hayashi, M.1    Denjoy, I.2    Extramiana, F.3
  • 36
    • 14744273673 scopus 로고    scopus 로고
    • Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations
    • Swan H., Laitinen P., Kontula K., and Toivonen L. Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations. J Cardiovasc Electrophysiol 16 (2005) 162-166
    • (2005) J Cardiovasc Electrophysiol , vol.16 , pp. 162-166
    • Swan, H.1    Laitinen, P.2    Kontula, K.3    Toivonen, L.4
  • 37
    • 0037220370 scopus 로고    scopus 로고
    • Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death
    • Sumitomo N., Harada K., Nagashima M., et al. Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death. Heart 89 (2003) 66-70
    • (2003) Heart , vol.89 , pp. 66-70
    • Sumitomo, N.1    Harada, K.2    Nagashima, M.3
  • 38
    • 34548201285 scopus 로고    scopus 로고
    • Calcium channel blockers and beta-blockers versus beta-blockers alone for preventing exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia
    • Rosso R., Kalman J.M., Rogowski O., et al. Calcium channel blockers and beta-blockers versus beta-blockers alone for preventing exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm 4 (2007) 1149-1154
    • (2007) Heart Rhythm , vol.4 , pp. 1149-1154
    • Rosso, R.1    Kalman, J.M.2    Rogowski, O.3
  • 39
    • 64149085800 scopus 로고    scopus 로고
    • Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans
    • Watanabe H., Chopra N., Laver D., et al. Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans. Nat Med 15 (2009) 380-383
    • (2009) Nat Med , vol.15 , pp. 380-383
    • Watanabe, H.1    Chopra, N.2    Laver, D.3
  • 40
    • 43249085697 scopus 로고    scopus 로고
    • Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia
    • Wilde A.A., Bhuiyan Z.A., Crotti L., et al. Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia. N Engl J Med 358 (2008) 2024-2029
    • (2008) N Engl J Med , vol.358 , pp. 2024-2029
    • Wilde, A.A.1    Bhuiyan, Z.A.2    Crotti, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.