Clinical characteristics and follow-up of complex arrhythmias associated with RYR2 gene mutations in children

被引:0
作者
Wang, Yefeng [1 ]
Yang, Yufan [2 ]
Xu, Ningan [3 ]
Xiao, Yunbin [1 ]
Zuo, Chao [1 ]
Chen, Zhi [1 ]
机构
[1] Cent South Univ, Hunan Childrens Hosp, Dept Cardiol, Affiliated Childrens Hosp,Xiangya Sch Med, Changsha, Peoples R China
[2] Cent South Univ, Hunan Childrens Hosp, Dept Pediat Intens Care Unit, Affiliated Childrens Hosp,Xiangya Sch Med, Changsha, Peoples R China
[3] Cent South Univ, Hunan Childrens Hosp, Dept Children Hlth, Affiliated Childrens Hosp,Xiangya Sch Med, Changsha, Peoples R China
基金
中国国家自然科学基金;
关键词
children; RyR2; gene; complex arrhythmias; atrial arrhythmias; gene mutation; POLYMORPHIC VENTRICULAR-TACHYCARDIA; EXPERT CONSENSUS STATEMENT; MANAGEMENT; PHENOTYPE;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective The aim of this study was to analyze the diagnosis, treatment, and follow-up of six cases of complex arrhythmias associated with RYR2 gene mutations in children. Method A retrospective analysis was conducted on six children diagnosed with complex arrhythmias associated with RYR2 gene mutations. The study included an analysis of the age of onset, initial symptoms, electrocardiographic characteristics, genetic results, treatment course, and follow-up outcomes. Results Among the six cases included in the study, there were four males and two females, with an average age of 3.5 +/- 0.5 years. The average time from initial symptoms to diagnosis was 2.7 +/- 1.3 years. The most common clinical manifestation was syncope, with exercise and emotions being the main triggers. All six children had de novo missense mutations in the RYR2 gene identified through whole-exome sequencing. In Holter electrocardiogram, atrial arrhythmias and sinoatrial node dysfunction were commonly observed in younger children. Four patients underwent exercise stress testing, with two experiencing bidirectional ventricular premature contractions and two experiencing bidirectional ventricular tachycardia and polymorphic ventricular tachycardia. Initial treatment involved oral propranolol or metoprolol. If arrhythmias persisted, flecainide or propafenone was added as adjunctive therapy. Two patients received permanent cardiac pacemaker treatment (single chamber ventricular pacemaker, VVI). All patients survived, with three experiencing occasional syncope during treatment. The follow-up period ranged from 12 to 37 months, with an average follow-up time of 24.3 +/- 3.7 months. Conclusion Complex arrhythmias associated with RYR2 gene mutations in children can present with various clinical manifestations. Atrial arrhythmias combined with sinoatrial node dysfunction are commonly observed in younger children, and the combination of pharmacological therapy and cardiac pacemaker treatment yields favourable treatment outcomes.
引用
收藏
页数:8
相关论文
共 18 条
[1]  
Al-Khatib SM, 2018, CIRCULATION, V138, pE272, DOI [10.1161/CIR.0000000000000549, 10.1161/CIR.0000000000000548]
[2]   CPVT: Arrhythmogenesis, Therapeutic Management, and Future Perspectives. A Brief Review of the Literature [J].
Baltogiannis, Giannis G. ;
Lysitsas, Dimitrios N. ;
di Giovanni, Giacomo ;
Ciconte, Giuseppe ;
Sieira, Juan ;
Conte, Giulio ;
Kolettis, Theofilos M. ;
Chierchia, Gian-Battista ;
de Asmundis, Carlo ;
Brugada, Pedro .
FRONTIERS IN CARDIOVASCULAR MEDICINE, 2019, 6
[3]   Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2) [J].
Bongianino, Rossana ;
Denegri, Marco ;
Mazzanti, Andrea ;
Lodola, Francesco ;
Vollero, Alessandra ;
Boncompagni, Simona ;
Fasciano, Silvia ;
Rizzo, Giulia ;
Mangione, Damiano ;
Barbaro, Serena ;
Di Fonso, Alessia ;
Napolitano, Carlo ;
Auricchio, Alberto ;
Protasi, Feliciano ;
Priori, Silvia G. .
CIRCULATION RESEARCH, 2017, 121 (05) :525-536
[4]   Sinus node dysfunction in catecholaminergic polymorphic ventricular tachycardia: Risk factor and potential therapeutic target? [J].
Faggioni, Michela ;
van der Werf, Christian ;
Knollmann, Bjorn C. .
TRENDS IN CARDIOVASCULAR MEDICINE, 2014, 24 (07) :273-278
[5]  
Kaneshiro Takashi, 2017, JACC Clin Electrophysiol, V3, P1062, DOI 10.1016/j.jacep.2017.04.017
[6]   Atropine-induced sinus tachycardia protects against exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia [J].
Kannankeril, Prince J. ;
Shoemaker, M. Benjamin ;
Gayle, Kathryn A. ;
Fountain, Darlene ;
Roden, Dan M. ;
Knollmann, Bjorn C. .
EUROPACE, 2020, 22 (04) :643-648
[7]   Efficacy of Flecainide in the Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia A Randomized Clinical Trial [J].
Kannankeril, Prince J. ;
Moore, Jeremy P. ;
Cerrone, Marina ;
Priori, Silvia G. ;
Kertesz, Naomi J. ;
Ro, Pamela S. ;
Batra, Anjan S. ;
Kaufman, Elizabeth S. ;
Fairbrother, David L. ;
Saarel, Elizabeth V. ;
Etheridge, Susan P. ;
Kanter, Ronald J. ;
Carboni, Michael P. ;
Dzurik, Matthew V. ;
Fountain, Darlene ;
Chen, Heidi ;
Ely, Wesley ;
Roden, Dan M. ;
Knollmann, Bjorn C. .
JAMA CARDIOLOGY, 2017, 2 (07) :759-766
[8]   Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Associated With Ryanodine Receptor (RyR2) Gene Mutations - Long-Term Prognosis After Initiation of Medical Treatment [J].
Kawata, Hiro ;
Ohno, Seiko ;
Aiba, Takeshi ;
Sakaguchi, Heima ;
Miyazaki, Aya ;
Sumitomo, Naokata ;
Kamakura, Tsukasa ;
Nakajima, Ikutaro ;
Inoue, Yuko Y. ;
Miyamoto, Koji ;
Okamura, Hideo ;
Noda, Takashi ;
Kusano, Kengo ;
Kamakura, Shiro ;
Miyamoto, Yoshihiro ;
Shiraishi, Isao ;
Horie, Minoru ;
Shimizu, Wataru .
CIRCULATION JOURNAL, 2016, 80 (09) :1907-1915
[9]   Catecholaminergic Polymorphic Ventricular Tachycardia [J].
Kim, Chan W. ;
Aronow, Wilbert S. ;
Dutta, Tanya ;
Frenkel, Daniel ;
Frishman, William H. .
CARDIOLOGY IN REVIEW, 2020, 28 (06) :325-331
[10]   The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome A Comprehensive Open Reading Frame Mutational Analysis [J].
Medeiros-Domingo, Argelia ;
Bhuiyan, Zahurul A. ;
Tester, David J. ;
Hofman, Nynke ;
Bikker, Hennie ;
van Tintelen, J. Peter ;
Mannens, Marcel M. A. M. ;
Wilde, Arthur A. M. ;
Ackerman, Michael J. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 54 (22) :2065-2074