Skip to main content
PMC home page
Journal of Atrial Fibrillation logoLink to Journal of Atrial Fibrillation
. 2014 Oct 31;7(3):1083. doi: 10.4022/jafib.1083

Evaluation Of Patients With Early Repolarization Syndrome

Saagar Mahida 1, Frederic Sacher 1, Benjamin Berte 1, Seigo Yamashita 1, Han Lim 1, Nicolas Derval 1, Arnaud Denis 1, Ashok Shah 1, Sana Amraoui 1, Meleze Hocini 1, Pierre Jais 1, Michel Haissaguerre 1
PMCID: PMC4956281  PMID: 27957112

Abstract

In recent years, the early repolarization pattern has emerged as a risk factor for malignant ventricular arrhythmias and sudden cardiac death. The identification of the subset of patients who are at high risk of sudden death represents a significant challenge to the clinician. Multiple clinical and ECG features have been associated with an increased risk of sudden deathin however the majority of risk factors confer a small increase in absolute risk. The present article reviews current evidence and potential management strategies in patients with early repolarization.

Introduction

The early repolarization pattern on the surface electrocardiogram (ECG) is a relatively common finding. The prevalence of early repolarizationin the general populations has been reported to be as high as 13%, although estimates have varied significantly between studies.[1-4] A higher prevalence has been reported in young males and individuals of African descent. The characteristic feature of the early repolarization pattern is elevation of the J point, which is the junction between the QRS complex and the ST segment.[5] J point elevation may manifest as slurring or notching of the terminal portion of the QRS complex.

The pattern of early repolarization described above has long been regarded as a benign ECG variant.[6] However in recent years, compelling evidence has emerged from a number of studies to suggest that early repolarization is associated with an increased risk of malignant ventricular arrhythmias and sudden cardiac death (Figure 1).In 2007, a seminal study from Haissaguerre et al,[7] which involved 206 patients with idiopathic ventricular fibrillation (VF) and 412 control subjects, demonstrated a significantly higher prevalence of early repolarizationin the VF group (31% in VF patients as compared to 5% in control patients).Two subsequent studies provided corroborating evidence linking early repolarization and arrhythmic sudden death. Rosso et al reported an approximately three-fold increase in the risk of sudden death associated with early repolarization (from 3.4/100,000 to 11/100,000).[8] In a large population-based study with follow-up extending beyond 30 years, Tikkanen et al also reported that early repolarization is associated with a significantly increased risk of sudden cardiac death.

Figure 1. Early repolarization and induction of VF.

Figure 1.

Open in a new tab

Surface ECG of patient with early repolarization demonstrating notching in the inferior and lateral leads.[24] Right image demonstrates a rhythm strip of the same patient with spontaneous induction of VF by a premature ventricular extrastimulus.

It is important to note that the definition of early repolarization has varied between population-based studies that have investigated the prognosis of this ECG variant. For instance, in a study from the 1960s, Wasserburger et al described early repolarization as an elevation of the ST segment at the J point of between 1 and 4 mm with an associated ST segment concavity in the mid and left precordial leads.[9] Subsequently, in the 1970s, Kambara and colleagues described it as an upward concave RS-T segment elevation, primarily in the precordial leads. They also described an associated slurring of the downstroke of the R wave, the presence of distinct J points, or both.[10] Both studies described early repolarization as a benign ECG variant. In contrast, the studies reporting an association between early repolarization and sudden death refer to a specific distinct entity. In these studies, early repolarization is defined as a pattern of J point elevation of >1 mm in 2 contiguous inferior and/or lateral leads[7] (Figure 1). The variations in the definition of early repolarization may account for some of the discrepancies in sudden death risk between studies.

Figure 2. ECG examples of slur and notch early repolarization patterns.

Figure 2.

Open in a new tab

The panel on the left demonstrates typical slur pattern with.The panel on the right demonstrates a notch pattern.

While the aforementioned studies have reported an association between early repolarization and sudden death, it is important to emphasize that the prevalence of sudden death amongst patients with this ECG pattern is very low. The identification of the subset of patients who are at high risk of sudden death represents a significant challenge. The present article reviews current evidence and potential management strategies in patients with early repolarization.

Genetic Basis Of Early Repolarization Syndrome

Multiple studies have previously demonstrated that ERS is a heritable disease.[7,11,12] The genetic substrate underlying ERS is currently poorly defined. While single gene mutations have been identified in isolated cases, a large proportion of the observed heritability remains unaccounted for.The first mutation underlying ERS was identified in a young patient from the original series from Haissaguerre et al. The mutation was located in a conserved residue in the KCNJ8 gene (S422L), which encodes an inwardly rectifying potassium channel. However the mutation was not functionally characterized.[13] In a subsequent study, Medeiros-Domingo et al who performed candidate-gene screening in 14 ERS patients and identified the mutation in one patient. The mutation was associated with a gain-of-function effect with an augmented IK-ATP current.[14] Further evidence implicating the KCNJ8-S422L variant came from a study by Barajas-Martinez et al. They also used a candidate-gene approach and identified a single ER patient with a KCNJ8- S422L mutation after screening 204 patients with a J wave syndrome.[15] They also reported a gain-of-function effect of the mutation.

Burashnikov et al performed candidate-gene screening in 24 ERS patients for mutations in genes encoding calcium channel subunits.[16] Four mutation carriers were identified; one mutation carrier had a CACNA1C mutation, two patients had CACNB2 mutations and one patient had a CACNA2D1 mutation. While the mutations were highly conserved, suggesting a potential pathogenic effect, they were not functionally validated. Watanabe et al performed candidate-gene screening for sodium channel (SCN5A) mutations in a cohort of 50 patients with ERS and ventricular fibrillation.[17] SCN5A mutations in highly conserved residues (A226D, L846R, and R367H) were identified in three unrelated ERS patients. Functional analysis of the mutations revealed loss-of-function type modulation with the mutant channels failing to generate an INa current.In a more recent study, Hu et al screened a cohort of 150 ERS and Brugada syndrome patients for mutations in ABCC9, which encodes the ATP-binding cassette transporter of IK-ATP (SUR2A).[18] Four ERS patients from the cohort were demonstrated to harbor a V734I-ABCC9 mutation. Functional analysis of the variant demonstrated a gain-of-function effect when co-expressed with the IK-ATP channel. The mutations identified to date have been summarized in Table 2.

Table 2. Genetic mutations identified by candidate-gene studies in ERS.

Gene Variants Gene product Functional effect No. patients Comment Ref
KCNJ8 S422L Inwardly rectifying potassium channel Gain-of-function effect with increased augmented IK-ATP current 221 3 unrelated ERS patients with same mutation identified in 3 different studies [13-15]
CACNA1C p.E850 del L type calcium channel, alpha subunit No functional analysis 24 [16]
CACNB2 S160T, R571C L type calcium channel, beta 2 subunit No functional analysis 24 2 unrelated ERS patients with different mutations [16]
CACNA2D1 S956T L type calcium channel, alpha 2/delta subunit 1 No functional analysis 24 [16]
SCN5A A226D, L846R, R367H Nav1.5 sodium channel alpha subunit Loss-of-function effect with loss of INa current 50 3 unrelated ERS patients with different mutations [17]
ABCC9 V734I ATP-binding cassette transporter of IK-ATP (SUR2A) Gain-of-function effect with augmented IK-ATP channel 150 (BrS and ERS) 4 unrelated ERS patients with same mutation [18]
Open in a new tab

Pathophysiological Mechanisms Underlying ERS

The first detailed insights into the mechanisms underlying ER came from Yan and Antzelevitch in 1996.[19] Using a wedge preparation from a canine ventricle they reported that the J wave is a manifestation of a transmural gradient of the action potential (AP) notch. Multiple ionic currents have been proposed to underlie the transmural dispersion of the AP notch including Ito, ICaL, IK-ATP and INa. Attenuation of the Ito current during administration the drug 4-AP significantly attenuates J wave amplitude.[19] Drugs that augment the IK-ATP current have been demonstrated to increase transmural dispersion of repolarization.[20] Further, as discussed above, mutations in genes encoding the IK-ATP channel have been reported to underlie ER.[13-15] Genetic studies have also identified mutations in genes encoding the ICaL, and INa currents, implying that these currents are potentially important mediators of altered repolarization in ER.[16,17]

The predilection of the ER pattern for the inferior and lateral ECG leads is not fully understood. It has been speculated that the ER pattern manifests in the leads associated with the left ventricle because of the transmural orientation of the mean vector axis across the left ventricle and the septum.[19] In terms of the mechanism of arrhythmia in ER, an augmented transmural repolarization gradient is predicted to precipitate phase 2 reentry and premature ventricular ectopics. In turn, interaction of the premature ventricular ectopics with a susceptible ventricular substrate is predicted to cause transmural re-entry.[21,22]

Risk Stratification Of Patients With Early Repolarization

A number of risk factors have been demonstrated to confer an increased risk of arrhythmic sudden death in patients with early repolarization.The following section outlines the evidence linking these risk factors with sudden death.

Clinical History

Haissaguerreet al demonstrated that39% of early repolarization syndrome (ERS) patients with cardiac arrest have a previous history of syncope. Further they reported that a history of aborted sudden death is associated with a 43% recurrence rate of ventricular arrhythmia.[7] In a subsequent study, Abe et al reported that 18.5% of patients with ERS had a previous history of syncope as opposed to only 2% in healthy controls.[23] More recently, Le Bloa et al reported that in 37 ERS patients with syncope, three patients had polymorphic VT during subsequent rhythm monitoring with an implantable loop recorder device.[24] Overall, these findings indicate that a history of unexplained syncope represents a potentially important risk factor for sudden death in ERS patients. Of note however, Bartczak and colleagues recently reported that amongst patients with syncope who are referred for tilt testing for suspected reflex syncope, the early repolarization variant was present in 31% of cases. These findings reflect the complexity of assessing ERS patients with syncope.[25]

The influence of a family history of sudden death on arrhythmic risk in ERS patients is presently unclear. Haissaguerre et al demonstrated that 14% of idiopathic VF patients with the ERS pattern have a family history of sudden death.[7] However in other studies, the reported familial aggregation is lower.[8] In a subset of patients with early repolarization, the trait has been observed to transmit with a monogenic pattern of inheritance. Gourraud et al identified four pedigrees with an autosomal dominant pattern of inheritance of ERS with a high incidence of sudden death amongst affected individuals.[12] In a study involving 363 relatives from 144 pedigrees, Nunn et al reported that the ERS pattern is more prevalent in relatives of sudden arrhythmic death cases as compared to controls (23% vs. 11%).[11] Overall, these findings suggest that a family history could potentially predict arrhythmic risk. However, further research is necessary to determine the influence of family history on sudden death risk.

ECG Features

Multiple ECG characteristics have been demonstrated to confer an increased risk of sudden death in ERS patients. Individual ECG risk factors are discussed in more detail below.

Inferior vs. Lateral J Wave Distribution

In a study involving a large cohort of ERS patients, Tikkanen et al demonstrated that inferior J point elevation is associated with a higher risk of sudden death (relative risk, 1.2843; P=0.03).[3]The specific risk of arrhythmic death was more elevated (relative risk, 1.43; P=0.03). Of note, the evidence linking lateral early repolarization with arrhythmic death was less robust. In a more recent study, Derval et al demonstrated that in patients with idiopathic VF, the J point elevation was more widespread as compared to that observed in patients with an established underlying cause of sudden death(4.3 ± 1.3 leads vs. 2.8 ± 0.8 leads; p=0.01).[26]

J Wave Amplitude

Tikkanen et al also reported that in a subset of patients with more pronounced J point elevation (>0.2 mV) in the inferior leads, the risk of sudden death was markedly elevated (relative risk, 2.983.94; P<0.001).[3] The relative risk of arrhythmic death was (3.94; P<0.001). Derval et al also demonstrated a higher J wave amplitude in idiopathic VF patients as compared to that observed in patients with an established underlying cause of sudden death (0.25 ± 0.11 mV vs. 0.13 ± 0.05 mV, p = 0.02).Further evidence linking augmented J point elevation came from Haissaguerre et al who demonstrated that in a significant proportion of ERS patients with VF, J point elevation is more pronounced immediately preceding episodes of ventricular arrhythmia.[7]

Horizontal vs. Ascending ST Segment

A horizontal or descending ST segment has been reported to be associated with a higher risk of sudden death as compared to a rapidly ascending ST segment. Tikkanen et al reported that subjects with early repolarization≥0.1 mV and a horizontal or descending ST segment had a relative risk of arrhythmic sudden death of 1.43.Amongst patients with inferior ER and a higher J wave amplitude (>0.2mV), the horizontal variant was associated with a relative risk of 3.14.[27] More pronounced J wave elevation was not demonstrated to alter risk in patients with ascending ST segment variant. In a smaller cohort of patients, Rosso et al provided further corroborating evidence linking the horizontal ST segment variant with increased risk of sudden death. They demonstrated that a horizontal ST segment has an odds ratio of sudden death of 13.8.[28] Finally, Rollin et al demonstrated that a horizontal ST segment is associated with an increased mortality HR of 8.75 (95% CI, 3.48 to 22.0).[29]

QRS Notching vs. Slurring

Notching of the terminal portion of the QRS has been reported to be more prevalent in patients with idiopathic VF. Merchant et al reported that QRS notching was more prevalent in the lateral leads in patients with ERS and VF as compared to controls (leads V4 (44% vs 5%, p = 0.001) and V5 (44% vs 8%, p = 0.006).Of note however, numbers of patients with ERS and VF in the study were small.[30] An example of an ECG illustrating notching is included in Figure 1.

Overall, the above findings suggest that the presence of inferior J point elevation of high amplitude with a horizontal down sloping pattern is the most ´malignant´ ECG in ERS patients. The evidence implicating this ECG pattern as a risk marker is less compelling.

Figure 3. ECG examples of horizontal and descending early repolarization patterns.

Figure 3.

Open in a new tab

The panel on the left demonstrates a typical horizontal ST segment. The panel on the right demonstrates an ascending ST segment pattern

Provocative Testing

Rotenet al investigated the effect of provocative testing with ajmaline in 31 patients with early repolarization and compared the response with 21 Brugada syndrome patients and 22 control patients. Interesting, in contrast to the observed response in Brugada syndrome patients, the degree of J point elevation was attenuated in early repolarization patients.[31] Corroborating evidence came from a study by Bastiaenenet al who demonstrated that ajmaline provocation results in diminished J point elevation, particularly in patients with lateral J point elevation and rapidly ascending ST segments.[32] Overall these findings indicate that sodium channel blockade does not play a role in risk stratification of early repolarization. Of note, in addition to sodium channel blockers, other pharmacological agents such as verapamil, epinephrine, ATP, cibenzoline, andpilsicainide have also have also been reported to have a negligible effect on the degree of J point elevation in ERS patients.[33]

Management Of ERS Patients

The early repolarization pattern is common in the general population and in the vast majority of patients, is associated with a benign prognosis. In asymptomatic patients with the early repolarization pattern, there is no indication for specific treatment.[34] In the small subset of patients who are deemed to be at high-risk, implantation of a cardiac defibrillator and/or pharmacological therapy maybe indicated.

Implantation of a cardiac defibrillator (ICD) is indicated in patients with early repolarization syndrome and previous aborted sudden death due to ventricular arrhythmia.[34]Patients with early repolarization and syncope on the other hand may represent a challenge. Extensive investigations to determine the cause of syncope are recommended.Patients with unexplained syncope may warrant close follow-up or rarely, ICD implantation. The presence of unexplainedsyncope with additional risk factors such as a ´malignant´ ECG with pronounced and wide spread J point elevation,a horizontal descending ST-segment,and a strong family history of sudden death at a young age may warrant ICD implantation.[34] Of note however, the evidence to support this strategy is less robust.

Pharmacological therapy maybe considered in early repolarization patients with an ICD and recurrent defibrillator shocks. A number of antiarrhythmics have been tried in this context. In a study by Haissaguerreet al involving 33 patients with early repolarization and recurrent ICD shocks intravenous isoproterenol was demonstrated to be effective in suppressing VF in the acute setting. Further, maintenance therapy with quinidine was demonstrated to suppress VF during longer-term follow-up.[33] By contrast, beta blockers, class 1C antiarrhythmics, and verapamil were demonstrated to be ineffective.The current recommendations for management of early repolarization patients from the HRS/EHRA/APHRS are summarized in Table 1.

Table 1. HRS/EHRA/APHRS guidelines for management of patients with early repolarization.

Abbreviations: ER, early repolarization; ECG, electrocardiogram; ICD, implantable cardiac defibrillator.

Class of evidence Treatment
Class I • ICD implantation is recommended in patients with a diagnosis of ER syndrome who have survived a cardiac arrest
Class IIa • Isoproterenolinfusion can beuseful in suppressing electrical storms in patients with a diagnosis of ER syndrome
• Quinidine in addition to an ICD can be useful for secondary prevention of VF in patients with a diagnosis of ER syndrome.
Class IIb • ICD implantation may be considered in symptomatic family members of ER syndrome patients with a history of syncope in the presence a definitive ER pattern on the ECG
• ICDimplantation may beconsidered in asymptomatic individualswhodemonstratea high-risk ERECGpattern(highJ-wave amplitude, horizontal/descendingSTsegment)in the presenceofastrongfamilyhistoryofjuvenile unexplained suddendeathwithorwithouta pathogenic mutation.
Class III • ICD implantation is not recommended asymptomatic patients with an isolated ER ECG pattern
Open in a new tab

Conclusion

While the vast majority of patients with early repolarization on the ECG will have a benign course, in a small but important subset this ECG pattern is associated with potentially catastrophic consequences. The major current challenge for the clinician is identifying these patients prior to the first episode of VF. Multiple ECG features have been reported to confer an increased risk of sudden death. It is important to note however that the majority of these risk factors are associated with modest increases in absolute risk and are therefore of limited clinical utility in isolation.[35] Further research is currently necessary to develop more robust risk-stratification algorithms.

Disclosures

None.

References

  1. Klatsky Arthur L, Oehm Rudolph, Cooper Robert A, Udaltsova Natalia, Armstrong Mary Anne. The early repolarization normal variant electrocardiogram: correlates and consequences. Am. J. Med. 2003 Aug 15;115 (3):171–7. doi: 10.1016/s0002-9343(03)00355-3. [DOI] [PubMed] [Google Scholar]
  2. Sinner Moritz F, Reinhard Wibke, Müller Martina, Beckmann Britt-Maria, Martens Eimo, Perz Siegfried, Pfeufer Arne, Winogradow Janina, Stark Klaus, Meisinger Christa, Wichmann H-Erich, Peters Annette, Riegger Günter A J, Steinbeck Gerhard, Hengstenberg Christian, Kääb Stefan. Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA). PLoS Med. 2010 Jul;7 (7):p. e1000314. doi: 10.1371/journal.pmed.1000314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Tikkanen Jani T, Anttonen Olli, Junttila M Juhani, Aro Aapo L, Kerola Tuomas, Rissanen Harri A, Reunanen Antti, Huikuri Heikki V. Long-term outcome associated with early repolarization on electrocardiography. N. Engl. J. Med. 2009 Dec 24;361 (26):2529–37. doi: 10.1056/NEJMoa0907589. [DOI] [PubMed] [Google Scholar]
  4. Gussak Ihor, George Samuel, Bojovic Bosko, Vajdic Branislav. ECG phenomena of the early ventricular repolarization in the 21 century. Indian Pacing Electrophysiol J. 2008;8 (3):149–57. [PMC free article] [PubMed] [Google Scholar]
  5. Derval Nicolas, Shah Ashok, Jaïs Pierre. Definition of early repolarization: a tug of war. Circulation. 2011 Nov 15;124 (20):2185–6. doi: 10.1161/CIRCULATIONAHA.111.064063. [DOI] [PubMed] [Google Scholar]
  6. Maury Philippe, Rollin Anne. Prevalence of early repolarisation/J wave patterns in the normal population. J Electrocardiol. 2013 Aug 29;46 (5):411–6. doi: 10.1016/j.jelectrocard.2013.06.014. [DOI] [PubMed] [Google Scholar]
  7. Haïssaguerre Michel, Derval Nicolas, Sacher Frederic, Jesel Laurence, Deisenhofer Isabel, de Roy Luc, Pasquié Jean-Luc, Nogami Akihiko, Babuty Dominique, Yli-Mayry Sinikka, De Chillou Christian, Scanu Patrice, Mabo Philippe, Matsuo Seiichiro, Probst Vincent, Le Scouarnec Solena, Defaye Pascal, Schlaepfer Juerg, Rostock Thomas, Lacroix Dominique, Lamaison Dominique, Lavergne Thomas, Aizawa Yoshifusa, Englund Anders, Anselme Frederic, O'Neill Mark, Hocini Meleze, Lim Kang Teng, Knecht Sebastien, Veenhuyzen George D, Bordachar Pierre, Chauvin Michel, Jais Pierre, Coureau Gaelle, Chene Genevieve, Klein George J, Clémenty Jacques. Sudden cardiac arrest associated with early repolarization. N. Engl. J. Med. 2008 May 8;358 (19):2016–23. doi: 10.1056/NEJMoa071968. [DOI] [PubMed] [Google Scholar]
  8. Rosso Raphael, Kogan Evgeni, Belhassen Bernard, Rozovski Uri, Scheinman Melvin M, Zeltser David, Halkin Amir, Steinvil Arie, Heller Karin, Glikson Michael, Katz Amos, Viskin Sami. J-point elevation in survivors of primary ventricular fibrillation and matched control subjects: incidence and clinical significance. J. Am. Coll. Cardiol. 2008 Oct 7;52 (15):1231–8. doi: 10.1016/j.jacc.2008.07.010. [DOI] [PubMed] [Google Scholar]
  9. WASSERBURGER R H, ALT W J. The normal RS-T segment elevation variant. Am. J. Cardiol. 1961 Aug;8 ():184–92. [Google Scholar]
  10. Kambara H, Phillips J. Long-term evaluation of early repolarization syndrome (normal variant RS-T segment elevation). Am. J. Cardiol. 1976 Aug;38 (2):157–6. doi: 10.1016/0002-9149(76)90142-9. [DOI] [PubMed] [Google Scholar]
  11. Nunn Laurence M, Bhar-Amato Justine, Lowe Martin D, Macfarlane Peter W, Rogers Pauline, McKenna William J, Elliott Perry M, Lambiase Pier D. Prevalence of J-point elevation in sudden arrhythmic death syndrome families. J. Am. Coll. Cardiol. 2011 Jul 12;58 (3):286–90. doi: 10.1016/j.jacc.2011.03.028. [DOI] [PubMed] [Google Scholar]
  12. Gourraud Jean-Baptiste, Le Scouarnec Solena, Sacher Frederic, Chatel Stéphanie, Derval Nicolas, Portero Vincent, Chavernac Pascal, Sandoval Juan E, Mabo Philippe, Redon Richard, Schott Jean-Jacques, Le Marec Hervé, Haïssaguerre Michel, Probst Vincent. Identification of large families in early repolarization syndrome. J. Am. Coll. Cardiol. 2013 Jan 15;61 (2):164–72. doi: 10.1016/j.jacc.2012.09.040. [DOI] [PubMed] [Google Scholar]
  13. Haïssaguerre Michel, Chatel Stéphanie, Sacher Frederic, Weerasooriya Rukshen, Probst Vincent, Loussouarn Gildas, Horlitz Marc, Liersch Ruedige, Schulze-Bahr Eric, Wilde Arthur, Kääb Stefan, Koster Joseph, Rudy Yoram, Le Marec Hervé, Schott Jean Jacques. Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel. J. Cardiovasc. Electrophysiol. 2009 Jan;20 (1):93–8. doi: 10.1111/j.1540-8167.2008.01326.x. [DOI] [PubMed] [Google Scholar]
  14. Medeiros-Domingo Argelia, Tan Bi-Hua, Crotti Lia, Tester David J, Eckhardt Lee, Cuoretti Alessandra, Kroboth Stacie L, Song Chunhua, Zhou Qing, Kopp Doug, Schwartz Peter J, Makielski Jonathan C, Ackerman Michael J. Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes. Heart Rhythm. 2010 Oct;7 (10):1466–71. doi: 10.1016/j.hrthm.2010.06.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Barajas-Martínez Hector, Hu Dan, Ferrer Tania, Onetti Carlos G, Wu Yuesheng, Burashnikov Elena, Boyle Madalene, Surman Tyler, Urrutia Janire, Veltmann Christian, Schimpf Rainer, Borggrefe Martin, Wolpert Christian, Ibrahim Bassiema B, Sánchez-Chapula José Antonio, Winters Stephen, Haïssaguerre Michel, Antzelevitch Charles. Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8. Heart Rhythm. 2012 Apr;9 (4):548–55. doi: 10.1016/j.hrthm.2011.10.035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Burashnikov Elena, Pfeiffer Ryan, Barajas-Martinez Héctor, Delpón Eva, Hu Dan, Desai Mayurika, Borggrefe Martin, Häissaguerre Michel, Kanter Ronald, Pollevick Guido D, Guerchicoff Alejandra, Laiño Ruben, Marieb Mark, Nademanee Koonlawee, Nam Gi-Byoung, Robles Roberto, Schimpf Rainer, Stapleton Dwight D, Viskin Sami, Winters Stephen, Wolpert Christian, Zimmern Samuel, Veltmann Christian, Antzelevitch Charles. Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. Heart Rhythm. 2010 Dec;7 (12):1872–82. doi: 10.1016/j.hrthm.2010.08.026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Watanabe Hiroshi, Nogami Akihiko, Ohkubo Kimie, Kawata Hiro, Hayashi Yuka, Ishikawa Taisuke, Makiyama Takeru, Nagao Satomi, Yagihara Nobue, Takehara Naofumi, Kawamura Yuichiro, Sato Akinori, Okamura Kazuki, Hosaka Yukio, Sato Masahito, Fukae Satoki, Chinushi Masaomi, Oda Hirotaka, Okabe Masaaki, Kimura Akinori, Maemura Koji, Watanabe Ichiro, Kamakura Shiro, Horie Minoru, Aizawa Yoshifusa, Shimizu Wataru, Makita Naomasa. Electrocardiographic characteristics and SCN5A mutations in idiopathic ventricular fibrillation associated with early repolarization. Circ Arrhythm Electrophysiol. 2011 Dec;4 (6):874–81. doi: 10.1161/CIRCEP.111.963983. [DOI] [PubMed] [Google Scholar]
  18. Hu Dan, Barajas-Martínez Hector, Terzic Andre, Park Sungjo, Pfeiffer Ryan, Burashnikov Elena, Wu Yuesheng, Borggrefe Martin, Veltmann Christian, Schimpf Rainer, Cai John J, Nam Gi-Byong, Deshmukh Pramod, Scheinman Melvin, Preminger Mark, Steinberg Jonathan, López-Izquierdo Angélica, Ponce-Balbuena Daniela, Wolpert Christian, Haïssaguerre Michel, Sánchez-Chapula José Antonio, Antzelevitch Charles. ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene. Int. J. Cardiol. 2014 Feb 15;171 (3):431–42. doi: 10.1016/j.ijcard.2013.12.084. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Yan G X, Antzelevitch C. Cellular basis for the electrocardiographic J wave. Circulation. 1996 Jan 15;93 (2):372–9. doi: 10.1161/01.cir.93.2.372. [DOI] [PubMed] [Google Scholar]
  20. Di Diego J M, Antzelevitch C. Pinacidil-induced electrical heterogeneity and extrasystolic activity in canine ventricular tissues. Does activation of ATP-regulated potassium current promote phase 2 reentry? Circulation. 1993 Sep;88 (3):1177–89. doi: 10.1161/01.cir.88.3.1177. [DOI] [PubMed] [Google Scholar]
  21. Meregalli Paola G, Wilde Arthur A M, Tan Hanno L. Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more? Cardiovasc. Res. 2005 Aug 15;67 (3):367–78. doi: 10.1016/j.cardiores.2005.03.005. [DOI] [PubMed] [Google Scholar]
  22. Koncz István, Gurabi Zsolt, Patocskai Bence, Panama Brian K, Szél Tamás, Hu Dan, Barajas-Martínez Hector, Antzelevitch Charles. Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome. J. Mol. Cell. Cardiol. 2014 Mar;68:20–8. doi: 10.1016/j.yjmcc.2013.12.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Abe Atsuko, Ikeda Takanori, Tsukada Takehiro, Ishiguro Haruhisa, Miwa Yosuke, Miyakoshi Mutsumi, Mera Hisaaki, Yusu Satoru, Yoshino Hideaki. Circadian variation of late potentials in idiopathic ventricular fibrillation associated with J waves: insights into alternative pathophysiology and risk stratification. Heart Rhythm. 2010 May;7 (5):675–82. doi: 10.1016/j.hrthm.2010.01.023. [DOI] [PubMed] [Google Scholar]
  24. LeBloa M, Sacher F, Maury P, Gourraud J, Mabot P, Leclercq C, Mansourati J, Babuty D, Hocini M, Laurent G, Jais P, Babuty D, Lamaison D, Pasquie J, Bordchar P, Furber A, Ritter P, Derval N, Klug D, Denis A, Rumeau P, Chavernac P, Boiffard E, Petit B, Hausman P, Haissaguere M, Probst V. Outcome of patients with syncope and early repolarization pattern. A multicentric prospective registry. in ESC congress. 2012. Munich: European Heart Journal. 2012;0:0–0. [Google Scholar]
  25. Bartczak Anna, Lelonek Malgorzata. Early repolarization variant in syncopal patients referred to tilt testing. Pacing Clin Electrophysiol. 2013 Apr;36 (4):456–61. doi: 10.1111/pace.12072. [DOI] [PubMed] [Google Scholar]
  26. Derval Nicolas, Simpson Christopher S, Birnie David H, Healey Jeffrey S, Chauhan Vijay, Champagne Jean, Gardner Martin, Sanatani Shubhayan, Yee Raymond, Skanes Allan C, Gula Lorne J, Leong-Sit Peter, Ahmad Kamran, Gollob Michael H, Haïssaguerre Michel, Klein George J, Krahn Andrew D. Prevalence and characteristics of early repolarization in the CASPER registry: cardiac arrest survivors with preserved ejection fraction registry. J. Am. Coll. Cardiol. 2011 Aug 9;58 (7):722–8. doi: 10.1016/j.jacc.2011.04.022. [DOI] [PubMed] [Google Scholar]
  27. Tikkanen Jani T, Junttila M Juhani, Anttonen Olli, Aro Aapo L, Luttinen Samuli, Kerola Tuomas, Sager Solomon J, Rissanen Harri A, Myerburg Robert J, Reunanen Antti, Huikuri Heikki V. Early repolarization: electrocardiographic phenotypes associated with favorable long-term outcome. Circulation. 2011 Jun 14;123 (23):2666–73. doi: 10.1161/CIRCULATIONAHA.110.014068. [DOI] [PubMed] [Google Scholar]
  28. Rosso Raphael, Glikson Eran, Belhassen Bernard, Katz Amos, Halkin Amir, Steinvil Arie, Viskin Sami. Distinguishing "benign" from "malignant early repolarization": the value of the ST-segment morphology. Heart Rhythm. 2012 Feb;9 (2):225–9. doi: 10.1016/j.hrthm.2011.09.012. [DOI] [PubMed] [Google Scholar]
  29. Rollin Anne, Maury Philippe, Bongard Vanina, Sacher Fréderic, Delay Marc, Duparc Alexandre, Mondoly Pierre, Carrié Didier, Ferrières Jean, Ruidavets Jean-Bernard. Prevalence, prognosis, and identification of the malignant form of early repolarization pattern in a population-based study. Am. J. Cardiol. 2012 Nov 1;110 (9):1302–8. doi: 10.1016/j.amjcard.2012.06.033. [DOI] [PubMed] [Google Scholar]
  30. Merchant Faisal M, Noseworthy Peter A, Weiner Rory B, Singh Sheldon M, Ruskin Jeremy N, Reddy Vivek Y. Ability of terminal QRS notching to distinguish benign from malignant electrocardiographic forms of early repolarization. Am. J. Cardiol. 2009 Nov 15;104 (10):1402–6. doi: 10.1016/j.amjcard.2009.06.062. [DOI] [PubMed] [Google Scholar]
  31. Roten Laurent, Derval Nicolas, Sacher Frédéric, Pascale Patrizio, Wilton Stephen B, Scherr Daniel, Shah Ashok, Pedersen Michala E F, Jadidi Amir S, Miyazaki Shinsuke, Knecht Sébastien, Hocini Mélèze, Jaïs Pierre, Haïssaguerre Michel. Ajmaline attenuates electrocardiogram characteristics of inferolateral early repolarization. Heart Rhythm. 2012 Feb;9 (2):232–9. doi: 10.1016/j.hrthm.2011.09.013. [DOI] [PubMed] [Google Scholar]
  32. Bastiaenen Rachel, Raju Hariharan, Sharma Sanjay, Papadakis Michael, Chandra Navin, Muggenthaler Martina, Govindan Malini, Batchvarov Velislav N, Behr Elijah R. Characterization of early repolarization during ajmaline provocation and exercise tolerance testing. Heart Rhythm. 2013 Feb;10 (2):247–54. doi: 10.1016/j.hrthm.2012.10.032. [DOI] [PubMed] [Google Scholar]
  33. Haïssaguerre Michel, Sacher Frederic, Nogami Akihiko, Komiya Nohiriro, Bernard Anne, Probst Vincent, Yli-Mayry Sinikka, Defaye Pascal, Aizawa Yoshifusa, Frank Robert, Mantovan Roberto, Cappato Riccardo, Wolpert Christian, Leenhardt Antoine, de Roy Luc, Heidbuchel Hein, Deisenhofer Isabel, Arentz Thomas, Pasquié Jean-Luc, Weerasooriya Rukshen, Hocini Meleze, Jais Pierre, Derval Nicolas, Bordachar Pierre, Clémenty Jacques. Characteristics of recurrent ventricular fibrillation associated with inferolateral early repolarization role of drug therapy. J. Am. Coll. Cardiol. 2009 Feb 17;53 (7):612–9. doi: 10.1016/j.jacc.2008.10.044. [DOI] [PubMed] [Google Scholar]
  34. Priori Silvia G, Wilde Arthur A, Horie Minoru, Cho Yongkeun, Behr Elijah R, Berul Charles, Blom Nico, Brugada Josep, Chiang Chern-En, Huikuri Heikki, Kannankeril Prince, Krahn Andrew, Leenhardt Antoine, Moss Arthur, Schwartz Peter J, Shimizu Wataru, Tomaselli Gordon, Tracy Cynthia. HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. Heart Rhythm. 2013 Dec;10 (12):1932–63. doi: 10.1016/j.hrthm.2013.05.014. [DOI] [PubMed] [Google Scholar]
  35. Obeyesekere Manoj N, Klein George J, Nattel Stanley, Leong-Sit Peter, Gula Lorne J, Skanes Allan C, Yee Raymond, Krahn Andrew D. A clinical approach to early repolarization. Circulation. 2013 Apr 16;127 (15):1620–9. doi: 10.1161/CIRCULATIONAHA.112.143149. [DOI] [PubMed] [Google Scholar]
  36. Zeller Tanja, Wild Philipp, Szymczak Silke, Rotival Maxime, Schillert Arne, Castagne Raphaele, Maouche Seraya, Germain Marine, Lackner Karl, Rossmann Heidi, Eleftheriadis Medea, Sinning Christoph R, Schnabel Renate B, Lubos Edith, Mennerich Detlev, Rust Werner, Perret Claire, Proust Carole, Nicaud Viviane, Loscalzo Joseph, Hübner Norbert, Tregouet David, Münzel Thomas, Ziegler Andreas, Tiret Laurence, Blankenberg Stefan, Cambien François. Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. PLoS ONE. 2010;5 (5):p. e10693. doi: 10.1371/journal.pone.0010693. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Atrial Fibrillation are provided here courtesy of CardioFront, LLC

RESOURCES