|Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutations.|
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|PMID: 22221940 Owner: NLM Status: MEDLINE|
|The aim of this study was to assess exercise test results and efficacy of therapy with a β blocker (acebutolol) in ryanodine receptor type 2 (RyR2) mutation carriers with documented ventricular arrhythmias (VAs) and long-term follow-up. Twenty RyR2 mutation carriers belonging to 8 families and regularly followed at our center were analyzed using a study protocol involving electrocardiography, exercise tests off and on β-blocker therapy, 2-dimensional echocardiography, and signal-averaged electrocardiography. Off-therapy exercise testing triggered the onset of VAs at different heart rates (mean 132 ± 13 beats/min) with various patterns that worsened while exercising and disappeared immediately after stopping. The most severe VAs detected were nonsustained ventricular tachycardia in 35% and ventricular couplets in 35%. In the remaining subjects single ventricular premature beats were recorded. In 15% of patients single monomorphic ventricular premature beats were detected and identified to be linked to RyR2 mutations owing to the presence of sudden deaths of their family members and subsequent family screening. Acebutolol made the VAs disappear completely in 20% of subjects and decreased their complexity in 50%, whereas it did not change VAs appreciably in 30% of patients with less complex VAs. After 11 ± 8 years of follow-up 2 patients developed syncope. In conclusion, exercise testing was a fundamental tool for assessing the clinical phenotype and efficacy of therapy in RyR2 mutation carriers and therapy with acebutolol led in most subjects to a decreased complexity of the arrhythmic pattern or to complete suppression.|
|Alexandros Klavdios Steriotis; Andrea Nava; Alessandra Rampazzo; Cristina Basso; Gaetano Thiene; Luciano Daliento; Antonio Franco Folino; Ilaria Rigato; Elisa Mazzotti; Giorgia Beffagna; Elisa Carturan; Domenico Corrado; Barbara Bauce|
|Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't Date: 2012-01-03|
|Title: The American journal of cardiology Volume: 109 ISSN: 1879-1913 ISO Abbreviation: Am. J. Cardiol. Publication Date: 2012 Apr|
|Created Date: 2012-03-26 Completed Date: 2012-05-18 Revised Date: 2014-03-19|
Medline Journal Info:
|Nlm Unique ID: 0207277 Medline TA: Am J Cardiol Country: United States|
|Languages: eng Pagination: 1015-9 Citation Subset: AIM; IM|
|Copyright Â© 2012 Elsevier Inc. All rights reserved.|
|APA/MLA Format Download EndNote Download BibTex|
Anti-Arrhythmia Agents / therapeutic use
Death, Sudden, Cardiac / prevention & control
Exercise Test* / adverse effects
Genetic Markers / genetics
Ryanodine Receptor Calcium Release Channel / genetics*
Tachycardia, Ventricular / diagnosis, drug therapy, etiology*, genetics
|0/Anti-Arrhythmia Agents; 0/Genetic Markers; 0/Ryanodine Receptor Calcium Release Channel; 67P356D8GH/Acebutolol|
Journal ID (nlm-ta): Am J Cardiol
Journal ID (iso-abbrev): Am. J. Cardiol
Publisher: Excerpta Medica
© 2012 Elsevier Inc.
Received Day: 30 Month: 9 Year: 2011
Revision Received Day: 23 Month: 11 Year: 2011
Accepted Day: 23 Month: 11 Year: 2011
pmc-release publication date: Day: 01 Month: 4 Year: 2012
Print publication date: Day: 01 Month: 4 Year: 2012
Volume: 109 Issue: 7
First Page: 1015 Last Page: 1019
PubMed Id: 22221940
Publisher Id: AJC18672
|Follow-Up with Exercise Test of Effort-Induced Ventricular Arrhythmias Linked to Ryanodine Receptor Type 2 Gene Mutations|
|Alexandros Klavdios Steriotisa⁎||Email: email@example.com|
|Antonio Franco Folinoa|
aDepartment of Cardiac, Thoracic, and Vascular Sciences, University of Padua, Padua, Italy
bDepartment of Biology, University of Padua, Padua, Italy
cDepartment of Medical Diagnostic Sciences and Special Therapies, University of Padua, Padua, Italy
|⁎Corresponding author: Tel.: 39-0498-218-642; fax: 39-0498-761-764 firstname.lastname@example.org
Ryanodine receptor type 2 (RyR2) has a pivotal role in regulating excitation–contraction coupling and sinoatrial node function.1–4 RyR2 mutations alter channel activity at adrenergic activation, increasing the likelihood of spontaneous calcium release during diastole, which is the basis for triggered and polymorphic ventricular arrhythmias (VAs).5–8 The main clinical entity is the catecholaminergic polymorphic ventricular tachycardia (VT), a highly malignant arrhythmogenic disorder prevalently present in a structurally normal heart, which is an important cause of sudden death in children and young adults.9–18 Exercise triggers the onset of a broad spectrum of VAs that progressively worsen, usually leading to a highly reproducible polymorphic or bidirectional VT that fades on stopping exercising.18–22 The aim of our study was to analyze exercise test findings in a group of RyR2 mutation carriers developing VAs while they were off and on β-blocker therapy and study the efficacy of a β blocker (acebutolol) over a lengthy follow-up.
From a cohort of 8 families (39 RyR2 mutation carriers) we selected 20 patients who carried 7 different RyR2 mutations, developed VAs during exercise testing, and were being monitored regularly. Silent mutation carriers (10 subjects without VAs during follow-up) and subjects with incomplete follow-up (9 subjects) were excluded. Our patients were heterozygous for RyR2 mutations: 6 carried the N2386I, 6 the A2387P, 2 the Y2392C, 2 the A77V, 2 the L433P, 1 the R420W, and 1 the M4504I. All mutations have been reported previously.9,12,17,23 Two patients were index cases identified with exercise testing before participation during a screening for competitive sports, and the remaining subjects were discovered through family screening because of a positive family history of sudden death during effort or emotion (13 subjects, mean age 19 ± 5.7 years). All subjects underwent electrocardiography, exercise testing, signal-averaged electrocardiography, and echocardiography with Doppler study.
The cycling exercise test was done using a 25-W × 2 protocol that assessed the first exercise tests performed off and on β blocker (within 1 month) and the last test performed on β blocker. Acebutolol, a β blocker with intrinsic sympathicomimetic activity, was chosen because it was used since the beginning in all patients, produces less arterial hypotension, and because of the good results on VAs was continued throughout the follow-up. All exercise tests were performed until onset of muscular fatigue or appearance of VT. Maximum heart rates (HRs) and workloads were recorded. The following features of VAs were analyzed: HR and workload at onset of VAs; most frequent ventricular premature beat (VPB) morphologies; episodes of ventricular bigeminy, ventricular couplets, VT, and corresponding HR; and behavior of VAs after stopping exercise. During the first exercise test off β blocker we also considered the mode of onset of VAs (coupling interval and morphology of the first VPB and corrected QT interval of the last sinus beat preceding onset of arrhythmia). Features of VAs under maximum exercising workload were recorded.
All continuous variables were expressed as mean ± SD. Student's paired and unpaired t tests were used to compare normally distributed data and Kruskal–Wallis test was used in all other cases. Chi-square test was used to compare noncontinuous variables expressed as proportions.
Twenty patients (8 men, 12 women) were analyzed. Their age at the time of baseline exercise tests was 27 ± 13 years and their age at the last test was 38 ± 13 years, so the mean follow-up was 11 ± 8 years (range 2 to 27).
Electrocardiography performed in the absence of therapy was considered normal in all patients. Sinus bradycardia at rest was found in 30%. Corrected QT interval was normal (mean 415 ± 24 ms). During follow-up 1 patient had a first-degree atrioventricular block and 1 a relatively short QT interval. Sinus bradycardia was recorded in another 2 patients. Follow-up electrocardiograms did not differ significantly from baseline in the remaining patients. On signal-averaged electrocardiogram late potentials were present in 4 subjects (20%) at the first assessment and at last follow-up.
Two-dimensional echocardiogram detected mild right ventricular dilation in 5 patients (25%) and 2 of them also had mild left ventricular dilation. One patient had right ventricular wall motion abnormalities (akinesia of the subtricuspid region and basal free wall). These findings did not change significantly during follow-up. None of the patients fulfilled the criteria for a definite diagnosis of arrhythmogenic right ventricular cardiomyopathy.24
For exercise testing off therapy the initiation, progression, and termination of VAs were studied (Table 1). Patients reached a maximum HR of 154 ± 17 beats/min (equivalent of 80 ± 8% of maximum HR predicted for age) and a maximum workload of 140 ± 58 W. Mean HR at onset of the first VPB was 132 ± 13 beats/min (minimum 115 beats/min, maximum 156 beats/min) under a mean workload of 111 ± 42 W. The coupling interval of the first VPB was 407 ± 30 ms. The corrected QT interval of the preceding sinus beat was 424 ± 22 ms. The first VPB revealed left bundle branch block or right bundle branch block morphology. VPBs with left bundle branch block morphology showed an inferior-axis deviation (75° to 105°) in 7 subjects and left-axis deviation (≤−30°) in 3 subjects. VPBs with right bundle branch block morphology showed left- or right-axis deviation in 9 subjects and a normal axis in 1. In 16 patients (80%) VAs began as monomorphic and became polymorphic as exercise progressed. In 3 patients (15%) VAs remained monomorphic during the entire exercise test. Ventricular bigeminy occurred in 75%, appearing at a mean HR of 144 ± 15 beats/min (minimum 130 beats/min, maximum 175 beats/min). Predominantly polymorphic ventricular couplets occurred in 70%, appearing at a mean HR of 145 ± 15 beats/min (minimum 125 beats/min, maximum 176 beats/min) and a workload of 129 ± 51 W. Polymorphic nonsustained VT was detected in 7 subjects (35%), occurring at a mean HR of 158 ± 16 beats/min (minimum 140 beats/min, maximum 175 beats/min) with a maximum ventricular rate of 191 ± 28 beats/min. Two subjects with nonsustained VT were index cases, and 5 were found during cascade screening and had the N2386I mutation. Under maximum workload the most severe VAs observed were nonsustained VTs in 35% and couplets in 30%, whereas single VPBs were detected in the remaining subjects. Overall, the most common VPB morphologies seen during exercise testing were characterized in 50% by left bundle branch block (35% with inferior-axis deviation, 15% with left-axis deviation) and in 35% by right bundle branch block (with variable-axis deviation), whereas the 2 morphologies were equally distributed in 15%. Stopping exercise led to the disappearance of VAs in all subjects immediately after or within the first minute of resting. Mean HR when the VAs disappeared differed significantly from the mean HR threshold (p = 0.03).
For baseline exercise testing on β-blocker therapy VAs disappeared completely in 15% of patients, nonsustained VTs disappeared, and couplets persisted in 20%. Therapy was effective in converting polymorphic to monomorphic patterns in 11 patients (55%). Maximum HR was decreased significantly compared to the test off β blocker, whereas mean maximum workload did not change significantly. Arrhythmias developed at a lower HR threshold than in the test off therapy (p = 0.03).
For exercise testing on therapy at the last follow-up, β-blocker dosage titration was needed in 10 patients. No significant differences emerged compared to results of the 2 exercise tests conducted on therapy (Table 1). Nonsustained VTs did not reappear, ventricular couplets decreased from 20% to 5%, and polymorphic patterns persisted in 30%. Comparing the first exercise test off therapy to the last on therapy, 14 patients (70%) responded to therapy. In detail, in 7 patients with nonsustained VT as the most severe arrhythmia, this arrhythmia disappeared (p = 0.006); in 7 patients with couplets as the most severe arrhythmia, this arrhythmia disappeared (p = 0.006); and in 6 patients with single VPBs, VPBs persisted throughout follow-up. During the last exercise test VPBs of left bundle branch block morphology persisted compared to right bundle branch block (60% vs 15%, p = 0.006). VPBs with left bundle branch block morphology presented inferior-axis deviation (45%) or left-axis deviation (15%). Mean HR threshold of the VAs decreased but not significantly and workload remained unchanged.
During follow-up only 2 patients became symptomatic. A 52-year-old woman had an implantable cardioverter–defibrillator because of an episode of syncope. A calcium channel blocker was added to β-blocker therapy. No further implantable cardioverter–defibrillator events or episodes of syncope were recorded during a 4-year follow-up. A 20-year-old woman developed syncope while dancing. Beta-blocker therapy was increased and no nonsustained VT appeared. Importantly, silent carriers were treated with β blocker and no VAs were recorded during follow-up.
RyR2 mutation carriers frequently have a family history of sudden death or they may present with effort-induced syncope or palpitations. Electrocardiogram is usually normal and late potentials may be present only in a minority of cases.17–19 Imaging techniques in most cases reveal normal findings.2,20 Exercise testing and Holter monitoring may often reveal VAs.22,25 Exercise testing is indicated for assessing subjects with known or suspected effort-induced VAs and ascertaining the efficacy of medical therapy. Antiarrhythmic strategies usually consist of high-dose β blockers; nadolol and propranolol are generally used.19 The antiarrhythmic effect is caused by an inhibition of the sympathetic action to β receptors and it may also improve RyR2 function by restoring the balance between phosphorylation and dephosphorylation and attenuate the increase of sarcoplasmic reticulum calcium content.2,4,5 Beta-blocker therapy is associated with lower event rates but usually fails to completely suppress VAs. Further studies on concomitant therapies (verapamil, flecainide, implantable cardioverter–defibrillator, left ventricular sympathetic denervation) are ongoing.26–29
In this study acebutolol was used; thus it contributes to further information on therapy for RyR2 mutation carriers. Furthermore, detailed analysis of arrhythmic patterns with and without therapy was assessed. Analysis of the first exercise test off therapy provided interesting information on features of the VA pattern. VAs occurred when a mean HR of 132 ± 13 beats/min and a workload of 111 ± 42 W were reached (Table 1). The first VPB did not show particular electrocardiographic characteristics. In most patients VAs appeared with a monomorphic pattern that became polymorphic as they continued to exercise. Ventricular bigeminy was common. With the increase of HR there was an exacerbation of VAs; couplets (145 ± 15 beats/min, p = 0.05) and nonsustained VTs (158 ± 16 beats/min, p = 0.000 01) appeared at a higher HR compared to onset of VAs. The low frequency of VT observed could be explained by the fact that only few patients exceeded their submaximal HR and only 2 patients were index cases. Moreover, phenotypic manifestations may be variable.20,22 All patients' VAs disappeared immediately or shortly after they stopped exercising, implicating the importance of the vagal reactivation.
The first exercise test on β blocker showed that the mean HR threshold of VAs decreased significantly (p = 0.03). A similar result was found at the end of follow-up by Haugaa et al30 using different β blockers. During the last exercise test the HR threshold decreased but not in a significant manner and importantly it was not accompanied by an increase of VA severity. Therapy with β blocker was able to decrease the maximum HR significantly, reaching the same level of workload as off therapy, thus not permitting more complex VAs to develop. Overall, in 20% VAs disappeared (p = 0.04). In 3 patients the decrease in maximum HR below the personal threshold of VAs could explain why no VAs occurred. The observation that further titration led to a decrease of VAs in only 1 more patient could be explained by the fact that maximum HR did not change significantly, probably because of intrinsic sympathicomimetic activity. In addition, β blocker was efficient in decreasing the complexity of the arrhythmic pattern in most patients, inhibiting the development of nonsustained VT, decreasing couplets significantly (to 5%), and decreasing polymorphic patterns (to 25%). Previous observations support the hypothesis that the β-blocker effect is caused by a decrease of maximum HR and additional mechanisms involved in the decrease of VAs.2,4,5
It is important to emphasize that 3 patients (15%) only had single monomorphic VPBs that remained monomorphic in 2 throughout follow-up. The prompt initiation of therapy does not permit us to predict if more complex arrhythmias could appear later in the absence of therapy. In these subjects the first exercise test alone could not distinguish idiopathic adrenergic VAs from those linked to RyR2 mutations because the latter were identified by family screening. Diagnosis was achieved by analyzing the family history of sudden death, demonstrating effort-induced polymorphic VPBs in other family members, and repeating the exercise test (which revealed a different VPB morphology in 1 subject). Identifying disease-causing RyR2 mutations through genetic screening confirms the diagnosis.
It is important to note that β-blocker therapy was unable to modify the arrhythmic pattern in 30% of patients characterized by single VPBs. Although a different type of β blocker was used in this study, the findings are similar to data published by Haugaa et al30 who reported no effect of β-blocker therapy in 43% of subjects and that less severe arrhythmias were not decreased despite the maximum tolerated dose of β blocker. The observation that noncomplex VAs persisted throughout follow-up could be interpreted as a protective mechanism of β blockers against more severe arrhythmias. Further studies in larger series are needed to establish whether some β blockers have greater efficacy than others and if their efficacy depends on the specific mutation on the RyR2 gene and severity of the arrhythmic pattern.
d31e444This study was supported by Grant GGP09293 from TELETHON, Rome, Italy; Fondazione CARIPARO, Padua, Italy; and the Registry of Cardio-Cerebro-Vascular Pathology, Veneto Region, Venice, Italy.
|1.||Vinogradova T.M.,Lakatta E.G.. Regulation of basal and reserve cardiac pacemaker function by interactions of cAMP-mediated PKA-dependent Ca2+ cycling with surface membrane channelsJ Mol Cell Cardiol47Year: 200945647419573534|
|2.||Blayney L.M.,Lai F.A.. Ryanodine receptor-mediated arrhythmias and sudden cardiac deathPharmacol Ther123Year: 200915117719345240|
|3.||Katz G.,Arad M.,Eldar M.. Catecholaminergic polymorphic ventricular tachycardia from bedside to bench and beyondCurr Probl Cardiol34Year: 200994319068246|
|4.||Jiang D.,Xiao B.,Yang D.,Wang R.,Choi P.,Zhang L.,Cheng H.,Chen S.R.. 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 A101Year: 2004130621306715322274|
|5.||Kashimura T.,Briston S.J.,Trafford A.W.,Napolitano C.,Priori S.G.,Eisner D.A.,Venetucci L.A.. In the RyR2(R4496C) mouse model of CPVT, β-adrenergic stimulation induces Ca waves by increasing SR Ca content and not by decreasing the threshold for Ca wavesCirc Res107Year: 20101483148920966392|
|6.||Paavola J.,Viitasalo M.,Laitinen-Forsblom P.J.,Pasternack M.,Swan H.,Tikkanen I.,Toivonen L.,Kontula K.,Laine M.. Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ wavesEur Heart J28Year: 20071135114217347175|
|7.||Katra R.P.,Oya T.,Hoeker G.S.,Laurita K.R.. Ryanodine receptor dysfunction and triggered activity in the heartAm J Physiol Heart Circ Physiol292Year: 2007H2144H215117189349|
|8.||Cerrone M.,Noujaim S.F.,Tolkacheva E.G.,O'Connell R.,Berenfeld O.,Anumonwo J.,Pandit S.V.,Vikstrom K.,Napolitano C.,Priori S.G.,Jalife J.. Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardiaCirc Res101Year: 20071039104817872467|
|9.||Tiso N.,Stephan D.A.,Nava A.,Bagattin A.,Devaney J.M.,Stanchi F.,Larderet G.,Brahmbhatt B.,Brown K.,Bauce B.,Muriago M.,Basso C.,Thiene G.,Danieli G.A.,Rampazzo A.. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)Hum Mol Genet10Year: 200118919411159936|
|10.||Laitinen P.J.,Brown K.M.,Piippo K.,Swan H.,Devaney J.M.,Brahmbhatt B.,Donarum E.A.,Marino M.,Tiso N.,Viitasalo M.,Toivonen L.,Stephan D.A.,Kontula K.. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardiaCirculation103Year: 200148549011157710|
|11.||Priori S.G.,Napolitano C.,Tiso N.,Memmi M.,Vignati G.,Bloise R.,Sorrentino V.,Danieli G.A.. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardiaCirculation103Year: 200119620011208676|
|12.||D'Amati G.,Bagattin A.,Bauce B.,Rampazzo A.,Autore C.,Basso C.,King K.,Romeo M.D.,Gallo P.,Thiene G.,Danieli G.A.,Nava A.. Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substratesHum Pathol36Year: 200576176716084945|
|13.||Medeiros-Domingo A.,Bhuiyan Z.A.,Tester D.J.,Hofman N.,Bikker H.,van Tintelen J.P.,Mannens M.M.,Wilde A.A.,Ackerman M.J.. 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 analysisJ Am Coll Cardiol54Year: 20092065207419926015|
|14.||Tester D.J.,Spoon D.B.,Valdivia H.H.,Makielski J.C.,Ackerman M.J.. Targeted mutational analysis of the RYR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's casesMayo Clin Proc79Year: 20041380138415544015|
|15.||Marjamaa A.,Laitinen-Forsblom P.,Wronska A.,Toivonen L.,Kontula K.,Swan H.. Ryanodine receptor (RyR2) mutations in sudden cardiac death: studies in extended pedigrees and phenotypic characterization in vitroInt J Cardiol147Year: 201124625219781797|
|16.||Basso C.,Carturan E.,Pilichou K.,Rizzo S.,Corrado D.,Thiene G.. Sudden cardiac death with normal heart: molecular autopsyCardiovasc Pathol19Year: 201032132520381381|
|17.||Bauce B.,Rampazzo A.,Basso C.,Bagattin A.,Daliento L.,Tiso N.,Turrini P.,Thiene G.,Danieli G.A.,Nava A.. Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriersJ Am Coll Cardiol40Year: 200234134912106942|
|18.||Postma A.V.,Denjoy I.,Kamblock J.,Alders M.,Lupoglazoff J.M.,Vaksmann G.,Dubosq-Bidot L.,Sebillon P.,Mannens M.M.,Guicheney P.,Wilde A.A.. Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patientsJ Med Genet42Year: 200586387016272262|
|19.||Liu N.,Ruan Y.,Priori S.G.. Catecholaminergic polymorphic ventricular tachycardiaProg Cardiovasc Dis51Year: 2008233018634915|
|20.||Priori S.G.,Napolitano C.,Memmi M.,Colombi B.,Drago F.,Gasparini M.,DeSimone L.,Coltorti F.,Bloise R.,Keegan R.,Cruz Filho F.E.,Vignati G.,Benatar A.,DeLogu A.. Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardiaCirculation106Year: 2002697412093772|
|21.||Nava A.,Canciani B.,Daliento L.,Miraglia G.,Buja G.,Fasoli G.,Martini B.,Scognamiglio R.,Thiene G.. Juvenile sudden death and effort ventricular tachycardias in a family with right ventricular cardiomyopathyInt J Cardiol21Year: 19881111263225065|
|22.||Horner J.M.,Ackerman M.J.. Ventricular ectopy during treadmill exercise stress testing in the evaluation of long QT syndromeHeart Rhythm5Year: 20081690169419084807|
|23.||Bagattin A.,Veronese C.,Bauce B.,Wuyts W.,Settimo L.,Nava A.,Rampazzo A.,Danieli G.A.. Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmiasClin Chem50Year: 20041148115515131021|
|24.||Marcus F.I.,McKenna W.J.,Sherrill D.,Basso C.,Bauce B.,Bluemke D.A.,Calkins H.,Corrado D.,Cox M.G.,Daubert J.P.,Fontaine G.,Gear K.,Hauer R.,Nava A.,Picard M.H.,Protonotarios N.,Saffitz J.E.,Sanborn D.M.,Steinberg J.S.,Tandri H.,Thiene G.,Towbin J.A.,Tsatsopoulou A.,Wichter T.,Zareba W.. Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task Force criteriaCirculation121Year: 20101533154120172911|
|25.||Sy R.W.,Gollob M.H.,Klein G.J.,Yee R.,Skanes A.C.,Gula L.J.,Leong-Sit P.,Gow R.M.,Green M.S.,Birnie D.H.,Krahn A.D.. Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardiaHeart Rhythm8Year: 201186487121315846|
|26.||Hayashi M.,Denjoy I.,Extramiana F.,Maltret A.,Buisson N.R.,Lupoglazoff J.M.,Klug D.,Hayashi M.,Takatsuki S.,Villain E.,Kamblock J.,Messali A.,Guicheney P.,Lunardi J.,Leenhardt A.. Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardiaCirculation119Year: 20092426243419398665|
|27.||Wilde A.A.,Bhuiyan Z.A.,Crotti L.,Facchini M.,De Ferrari G.M.,Paul T.,Ferrandi C.,Koolbergen D.R.,Odero A.,Schwartz P.J.. Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardiaN Engl J Med358Year: 20082024202918463378|
|28.||Watanabe H.,Chopra N.,Laver D.,Hwang H.S.,Davies S.S.,Roach D.E.,Duff H.J.,Roden D.M.,Wilde A.A.,Knollmann B.C.. Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humansNat Med15Year: 200938038319330009|
|29.||Van der Werf C.,Kannankeril P.J.,Sacher F.,Krahn A.D.,Viskin S.,Leenhardt A.,Shimizu W.,Sumitomo N.,Fish F.A.,Bhuiyan Z.A.,Willems A.R.,van der Veen M.J.,Watanabe H.,Laborderie J.,Haïssaguerre M.,Knollmann B.C.,Wilde A.A.. Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardiaJ Am Coll Cardiol57Year: 20112244225421616285|
|30.||Haugaa K.H.,Leren I.S.,Berge K.E.,Bathen J.,Loennechen J.P.,Anfinsen O.G.,Früh A.,Edvardsen T.,Kongsgård E.,Leren T.P.,Amlie J.P.. High prevalence of exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia mutation-positive family members diagnosed by cascade genetic screeningEuropace12Year: 201041742320106799|
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