Inherited arrhythmia syndrome predisposing to sudden cardiac death

Abstract

Inherited arrhythmia (IA) is one of the main causes of sudden cardiac death (SCD) in young people, and is reported to be a more prevalent cause of SCD in Asia than in Western countries. IAs are a group of genetic disorders caused by mutations in genes encoding cardiac ion channels, leading to electrophysiological characteristics that often occur in the absence of structural abnormalities. Channelopathies, such as long QT syndrome and Brugada syndrome, carry a potential risk of life-threatening ventricular tachyarrhythmias that predispose to SCD, although early prediction and prevention of the risk remain challenging. Recent advances in genetic testing have facilitated risk stratification as well as a precise diagnosis for IA, despite ongoing debates about the implications. Herein, we provide epidemiological data, a pathophysiological overview, and the current clinical approach to IAs related to SCD. In addition, we review the general issues arising from genetic testing for IAs.

INTRODUCTION

Sudden cardiac death (SCD) is a major global health burden [1,2]. A substantial proportion of SCD is related to coronary artery disease and heart failure [1,3]. However, SCD can occur in healthy patients without overt heart disease.4 These non-structural causes of SCD often occur in relatively young patients without prior heart disease and are referred to as inherited arrhythmia (IA) syndrome [3,4]. When appropriate resuscitation is not performed during the acute event, IA can cause grave damage both to the patient and to his or her family. The underlying pathophysiology of IA has not been fully established; however, recent advances in technology for molecular biology and high throughput testing have uncovered the genetic basis for IA syndrome, which has enabled identification and targeting of the culprit substrate [3,5].

IA consists mainly of cardiac channelopathies such as Brugada syndrome (BrS), long QT syndrome (LQTS), short QT syndrome (SQTS), and catecholaminergic polymorphic ventricular tachycardia (CPVT) [3,6–8]. Early repolarization syndrome (ERS) and idiopathic ventricular fibrillation (IVF) are other primary electrical disorders. Nonischemic cardiomyopathies, such as hypertrophic cardiomyopathy, dilated cardiomyopathy, or arrhythmogenic right ventricular cardiomyopathy (ARVC), are also genetic disorders that have a risk of SCD.

The IAs have certain clinical characteristics. First, the initial manifestation may be lethal or a severe form like cardiac arrest or syncope due to ventricular tachyarrhythmias. Second, diagnosis of the disease and prediction for SCD may be difficult because of a lack of clinical clues, and structural abnormalities in imaging studies are rare. Third, IA is a genetic or familial disease, and is not curable. Fourth, primary prevention for SCD in clinical practice using an implantable cardioverter-defibrillator (ICD) is still controversial.

In this review, we provide epidemiological, clinical and genetic overviews of IAs that predispose to SCD. In addition, we provide a current update to the clinical approach and genetic testing for IA.

EPIDEMIOLOGY OF SCD AND INHERITED ARRHYTHMIAS

The estimated incidence of SCD in North America and Europe is 50–100 cases per 100,000 person-years of follow-up [6,9,10]. The incidence is higher in people older than 35 years with one case per 1,000 person-years of follow-up; however, the risk of SCD is not negligible in people younger than 35 years [11]. SCD can occur not only by ventricular fibrillation (VF) or ventricular tachycardia (VT) but also with pulseless electrical activity or asystole. Furthermore, VF and VT can degenerate into pulseless electrical activity or asystole if left untreated. Estimation of the incidence of IA is made more complicated because substantial proportions of VF and VT are due to structural heart disease such as coronary artery atherosclerosis [12]. According to data from Western countries, coronary artery disease is responsible for 60% to 80% of SCD, while the proportion of SCD with underlying IA is < 5% [13,14]. However, Japanese data indicated that primary electrical disorders related to channelopathies were estimated to be responsible for 10% of SCDs [15]. The proportion of IA in people who experienced SCD in South Korea may be higher than in Western countries and similar to or higher than in Japan. Based on the Korean National Health Insurance Service database, among 1,125,691 people included in the sample cohort, the overall incidence of sudden cardiac arrest was 48.7 per 100,000 person-years, and the rate of sudden unexplained death was 14.7% in patients with SCD [16]. Roh et al. [17] also demonstrated that among patients who received an ICD, identified using the Health Insurance Review and Assessment Service database, the proportion of IA as an etiology associated with the ICD was 21.1%. According to data from the Korean Inherited Arrhythmia Registry, among 265 probands clinically diagnosed with IAs, IVF was the most common (n = 99, 37.3%), followed by BrS (n = 90, 34.0%) and LQTS (n = 54, 20.4%), and among 128 family members, about half were related to a patient with BrS (n = 62, 48.4%), followed by LQTS (n = 39, 30.5%) and IVF (n = 19, 14.8%) (Fig. 1) [18]. The three most common IAs (BrS, IVF, and LQTS) accounted for > 90% of IAs in the probands and their family members in the Korean population.

Figure 1.

Distribution of inherited arrhythmias in probands (A) and their family members (B) in the Korean population [18]. ARVC, arrhythmogenic right ventricular cardiomyopathy; BrS, Brugada syndrome; CPVT, catecholaminergic polymorphic ventricular tachycardia; ERS, early repolarization syndrome; IVF, idiopathic ventricular fibrillation; LQTS, long QT syndrome; SQTS, short QT syndrome.

CLINICAL APPROACH TO INHERITED ARRHYTHMIA SYNDROME

Excitation contraction coupling in the cardiomyocyte is a core process generating heart rhythm, which is mediated by harmonized ionic currents through various ion channels that are imbedded in the sarcolemma. Alterations in the function of cardiac ion channels by genetic mutations can cause electrical heterogeneity and subsequent initiation of ventricular tachyarrhythmias, which are called channelopathies. Gain- or loss-of-function of cardiac ion channels reveal no structural abnormalities of the heart in imaging studies. Major forms of channelopathies responsible for SCD include BrS, LQTS, SQTS, CPVT, ERS, and IVF [19–22]. The overall diagnostic approach is summarized in Fig. 2. The underlying genetic pathophysiology and a current clinical update of the channelopathies are reviewed in the following section.

Figure 2.

A diagnostic algorithm in inherited arrhythmia syndrome. LQTS, long QT syndrome; CPVT, catecholaminergic polymorphic ventricular tachycardia; SQTS, short QT syndrome; ARVC, arrhythmogenic right ventricular cardiomyopathy; ECG, electrocardiogram; CAG, coronary angiography; SA, signal averaged; EP, electrophysiological; QTc, corrected QT; VT, ventricular tachycardia; DDx, differential diagnosis; MRI, magnetic resonance image; CT, computed tomography; RV, right ventricle; VF, ventricular fibrillation. ^aBazett or Fridericia formula: standard and upper level (up to the 2nd or 3rd intercostal space), ^bEpinephrine for LQTS, CPVT: procainamide or flecainide for Brugada syndrome, ^cNext-generation sequencing panels for channelopathies and cardiomyopathies.

LONG QT SYNDROME

Patients with LQTS experience lethal ventricular arrhythmias accompanied by prolongation of the QT interval reflecting an excessive prolongation in the duration of cardiac repolarization (Fig. 3). An epinephrine challenge test can unmask prolongation of the QT interval in patients with ‘concealed LQTS’ who show a normal range of QT intervals on their resting electrocardiography (ECG). Patients with LQTS are diagnosed by an LQTS risk score > 3, a corrected QT (QTc) interval for heart rate using Bazett’s formula ≥ 480 ms in repeated ECGs in the absence of a secondary cause for QT prolongation, or an unequivocally pathogenic mutation in one of the LQTS genes [23]. Among 20 genes that have been discovered, potassium voltage-gated channel subfamily Q member 1 (KCNQ1; LQT1), potassium voltage-gated channel subfamily H member 2 (KCNH2; LQT2), and sodium voltage-gated channel alpha subunit 5 (SCN5A; LQT3) are the most common LQTS genes, accounting for about 90% [3,20,24,25]. Triggers for cardiac events and ECG morphologies that may be characteristic according to the genotypes can assist in management [26]. Affected patients show high mortality rates > 20% within 1 year after the first syncopal episode if left untreated [26,27]. Schwartz reported a significantly reduced mortality in LQTS patients who received beta-blocker or surgical antiadrenergic therapy [27]. Patients with genetic LQTS treated with a beta-blocker experience a high rate of cardiac events, particularly those with LQT2 and LQT3 genotypes [28]. Recent studies have demonstrated the superiority of nadolol, a beta-blocker, in reducing the risk of life-threatening arrhythmic events, suggesting preferential management with nadolol [29,30]. An ICD with the use of a beta-blocker is recommended in LQTS patients with previous cardiac arrest. Left cardiac sympathetic denervation should be considered when a beta-blocker is either not effective, not tolerated or contraindicated, or when an ICD is contraindicated or refused [22]. Table 1 shows the clinical characteristics of LQTS in Korean and international registries [18,31–35].

Figure 3.

A 24-year-old female patient’s electrocardiographies showed marked prolongation of the QT interval and subsequent polymorphic ventricular tachycardia (PMVT) (top). Her genetic testing result was a positive genotype of potassium voltage-gated channel subfamily H member 2 (KCNH2). She was diagnosed with long QT syndrome (LQTS) type 2. The mechanism of lethal ventricular tachyarrhythmia in LQTS (bottom). PVC, premature ventricular contraction.

Table 1.

Clinical characteristics of patients with LQTS in international registries

Characteristic	Korean IA registry [18] (n = 54)	Korean single center [31] (n = 62)	Burns et al. [32] (Austrailia) (n = 78)	Earle et al. [33] (New Zealand) (n = 309)	Goldenberg et al. [34] (7 multi-national) (n = 1,861)	Sauer et al. [35] (international LQTS registry) (n = 812)
Mean age, yr	38 ± 17	15.8	40 ± 18	30	NA	32
Female sex	42 (78)	34 (55)	57 (73)	184 (60)	1,075 (58)	469 (58)
History of syncope	18 (33)	26 (42)	39 (50)	72 (23)	655 (35)	NA
History of SCD	27 (50)	15 (24)	25 (32)	48 (16)	191 (10)	NA
Family history of SCD	8 (15)	NA	NA	40 (13)	NA	NA
ICD implantation	33 (61)	6 (10)	40 (51)	NA	223 (12)	9 (1)
QTc interval, msec	504	539	515	480	480	489
Beta-blocker	41 (76)	41 (66)	66 (85)	NA	930 (50)	149 (18)

Values are presented as mean ± SD or number (%).

LQTS, long QT syndrome; IA, inherited arrhythmia; NA, not available; SCD, sudden cardiac death; ICD, implantable cardioverter defibrillator; QTc, corrected QT.

BRUGADA SYNDROME

BrS is an inherited disorder associated with lethal ventricular arrhythmias and results in an increased risk of SCD [36]. BrS is diagnosed in patients with ST-segment elevation with type 1 morphology ≥ 2 mm in one or more leads among the right precordial leads V1 and/or V2, positioned in the second, third, or fourth intercostal space, occurring either spontaneously or after a provocative drug test with intravenous or oral administration of sodium channel blockers, such as flecainide or procainamide [22]. Brugada phenocopies, which are Brugada-like ECG patterns induced by reversible conditions such as pectus excavatum, should be differentiated from true BrS [37]. Lethal arrhythmias occur predominantly in younger males (20 to 40 years old) during rest or sleep [38]. Among 19 genes known to be associated with BrS, loss-of-function in SCN5A, CACN1AC, and sodium voltage-gated channel alpha subunit 10 (SCN10A) were found individually in > 5% of positively genotyped patients [39]. However, the clinical use of genetic testing results remains limited, which may be due to oligogenic genetic susceptibility and low disease penetrance in BrS compared to forms of Mendelian inheritance [40]. In addition, a subset of patients with BrS also have other types of arrhythmias such as atrial fibrillation or conduction defects such as atrioventricular block [3,41,42]. Lifestyle modification is recommended in all patients with a diagnosis of BrS [23]. Drugs that may induce ST-segment elevation in right precordial leads, excessive alcohol intake, and large meals should be avoided; any fever should be promptly treated with antipyretics. An ICD is recommended in survivors of an aborted cardiac arrest or patients who have documented sustained VT, and should be considered in patients with a spontaneous type I ECG pattern and history of syncope, presumably due to an episode of VT. Table 2 shows the clinical characteristics of BrS in Korean and international registries [18,38,43–49].

Table 2.

Clinical characteristics of patients with BrS in international registries

Characteristic	Korean IA Registry [18] (n = 90)	Japanese multi-center registry [43] (n = 415)	Sieira et al. [44] (Belgium) (n = 404)	Delise et al. [45] (Italy) (n = 320)	FINGER registry [46] (n = 1,029)	Eckardt et al. [47] (Europe) (n = 212)	Brugada et al. [48] (Europe) (n = 443)	Priori et al. [38] (Italy) (n = 200)	Brugada et al. [49] (n = 334)
Mean age, yr	41 ± 13	46 ± 14	43 ± 16	43	45	45 ± 6	42 ± 14	41 ± 18	42 ± 16
Male sex	84 (93)	403 (97)	235 (58.2)	258 (81)	745 (72)	152 (72)	342 (77)	152 (76)	225 (67)
History of syncope	27 (30)	99 (24)	114 (28)	105 (34)	313 (30)	65 (31)	100 (23)	34 (17)	73 (22)
History of SCD	50 (56)	88 (21)	17 (4.2)	NA	62 (6)	24 (11)	80 (18)	22 (11)	71 (21)
Family history of SCD	23 (26)	64 (15)	187 (47)	94 (29)	264 (26)	60 (28)	NA	26/130 (22)	180 (54)
ICD implantation	70 (78)	241 (58)	168 (42)	110 (34)	433 (42)	113 (53)	NA	52 (26)	129 (39)
Type I ECG	50/56 (89)	299 (72)	NA	174 (54)	468 (45)	125 (59)	NA	90/176 (51)	NA
SCN5A genotype	NA	60 (14)	53 (22)	NA	185 (18)	57/183 (31)	NA	28/130 (22)	NA

Values are presented as mean ± SD or number (%).

BrS, Brugada syndrome; IA, inherited arrhythmia; FINGER, France, Italy, Netherlands, GERmany; SCD, sudden cardiac death; NA, not available; ICD, implantable cardioverter defibrillator; ECG, electrocardiogram; SCN5A, sodium voltage-gated channel alpha subunit 5.

EARLY REPOLARIZATION SYNDROME

Electrocardiographic characteristics of early repolarization include J-point (the point between the end of the QRS complex and the beginning of the ST segment) elevation, notching or slurring of the terminal part of the QRS complex, and tall and symmetric T waves (Fig. 4) [50]. Previously, early repolarization was considered a benign phenomenon that did not need further evaluation [51,52]. However, the concept has changed since the demonstration that early repolarization in ECG, particularly in the inferior and lateral leads and with greater amplitude, is associated with a significantly increased risk of lethal ventricular arrhythmias and SCD [53–55]. The term ERS is used when early repolarization shown in ECG is accompanied by clinical symptoms such as syncope or SCD. The underlying mechanism for J-point elevation and the occurrence of lethal ventricular arrhythmias in ERS has still not been fully elucidated. A voltage gradient that results from transmural differences between the epicardium and endocardium during phases 1 and 2 of the cardiac action potential has been suggested as a possible mechanism of J-point elevation by Antzelevitch et al. [50,56,57]. They also suggested that eliminating the arrhythmia substrate might reduce the future recurrence of lethal ventricular arrhythmias [58,59]. Several novel genetic variations in potassium inwardly rectifying channel subfamily J member 8 (KCNJ8) and SCN5A have been reported to be potential genetic abnormalities responsible for ERS [60,61].

Figure 4.

Electrocardiogram in a 26-year-old man showed early repolarization syndrome with prominent J waves (arrows) in inferolateral leads (top). Implantable cardioverter defibrillator examination demonstrated an episode of sudden onset ventricular fibrillation (bottom).

IDIOPATHIC VENTRICULAR FIBRILLATION

IVF is diagnosed when no other cause is identified despite a systematic evaluation including ECG, imaging studies, drug challenge test and genetic evaluation in patients suffering VF. The Heart Rhythm Society/European Heart Rhythm Association/Asia Pacific Heart Rhythm Society expert consensus defines IVF as a resuscitated cardiac arrest victim, preferably with documentation of VF, in whom known cardiac, respiratory, metabolic and toxicological causes have been excluded through clinical evaluation [62,63]. The possibility of IAs or cardiomyopathies should be excluded before making the diagnosis of IVF. Whether IVF is caused by variations in a single or multiple genes is unclear. Interactions between genetic variations and environmental factors such as electrolyte imbalance, sympathetic activities, and undetectable myocardial fibrosis may also play a role [63]. Genetic testing in collaboration with clinical evaluation can facilitate identification of the underlying pathophysiology of IVF. With recent advances in genetic testing and detection of a clinical subset of IVF, the incidence of IVF is expected to decline [63]. Although cardiomyopathies are not part of IA syndrome due to obvious structural abnormalities, a lethal ventricular arrhythmia can be the first manifesting symptom [64]. Evaluating whether these concealed cardiomyopathies are associated with an increased risk of lethal ventricular arrhythmia will evolve with molecular diagnostics. Table 3 shows the clinical characteristics of IVF in Korean and international registries [18,65–70].

Table 3.

Clinical characteristics of patients with IVF in international registries

Characteristic	Korean IA registry [18] (n = 99)	Herman et al. [65] (n = 119)	Remme et al. [66] (n = 37)	Champgne et al. [67] (n = 18)	Meissner et al. [68] (n = 28)	Mewis et al. [69] (n = 18)	Crijns et al. [70] (n = 10)
Mean age, yr	41	48	35	42	42	48	37
Female sex	18 (22)	46 (39)	11 (30)	5 (28)	13 (46)	9 (50)	2 (20)
ICD implantation	88 (89)	111 (93)	23 (62)	18 (100)	28 (100)	5/18 (28)	1 (10)
VF recurrence	NA	10/89 (11)	16 (43)	7 (39)	2 (11)	0	NA

Values are presented as number (%).

IVF, idiopathic ventricular fibrillation; IA, inherited arrhythmia; ICD, implantable cardioverter defibrillator; VF, ventricular fibrillation; NA, not available.

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY

Arrhythmogenic cardiomyopathy is a genetically determined abnormality of cardiac desmosomes predisposing to SCD, particularly in young patients and athletes. Although involvement is often biventricular, predominant involvement of the right ventricle is the original disease phenotype, hence ARVC. The histopathological hallmark of ARVC is the substitution of right ventricular myocardium with fatty or fibrous tissue [71,72]. Prior studies have revealed that the disease is caused by genetic variations in genes encoding cardiac desmosomes such as junction plakoglobin (JUP), desmoplakin (DSP), plakophilin 2 (PKP2), desmoglein 2 (DSG2), and desmocollin 2 (DSC2) [73–77]. Patients with ARVC usually have structural abnormalities such as right ventricular dilation or wall thinning [78]. The diagnosis of ARVC may be difficult due to highly variable clinical presentations [79]. In the early phase, affected patients are at increased risk of lethal ventricular arrhythmias, but show no evidence of right ventricular abnormality and clinical symptoms; this is known as a concealed phase [79]. SCD can be the first clinical manifestation in patients affected by ARVC [80]. Therefore, although ARVC is a cardiomyopathy with structural abnormalities, it can also be called an IA syndrome in which lethal ventricular arrhythmia occurs without obvious structural abnormality in the heart.

Cerrone et al. [81] demonstrated the coexistence of sodium channelopathy and genetic PKP2 variations, suggesting PKP2 mutations may be a molecular substrate leading to the diagnosis of BrS. Accordingly, the overlapping phenotype may be explained by the emerging theory that ARVC and BrS are not completely different conditions, but the ends of a spectrum of structural myocardial abnormalities and sodium current deficiency that share a common origin as diseases of the connexome [82].

GENETIC TESTING FOR INHERITED ARRHYTHMIAS

In the past, the underlying causes of IA were not identifiable due to technical limitations. However, as advances in genetics have improved the understanding of IAs, genetic testing for the channelopathies and cardiomyopathies can have diagnostic, prognostic, and therapeutic implications, potentially influencing clinical decisions (Table 4) [23,43,62,83–85]. Recently, the next-generation sequencing technique has enabled multiple genetic variant analysis in a given patient, within a reasonable cost and time requirement. However, not all physicians can incorporate the results of genetic testing into a patient’s care, because of potential pitfalls. Unlike solid cancers that are caused by somatic variants, the main outcome measurement in patients with IAs that are mostly caused by germline variants is an event of SCD (i.e., ‘all or nothing’), which is hard to predict. Standards and guidelines developed by the American College of Medical Genetics and Genomics can be used for the interpretation of sequence variants using five specific categories based on evidence: ‘benign,’ ‘likely benign,’ ‘variants of unknown significance,’ ‘likely pathogenic,’ and ‘pathogenic’ [86]. More expertise is required to interpret the results of various genetic evaluations. Proper genetic sampling, sample processing, adequate sequencing, and precise interpretation, correlated with the clinical situation, constitute the core competence in the field of cardiovascular genetics.

Table 4.

Summary of genetic testing for inherited arrhythmias in clinical practice based on current guidelines and evidence [23,43,62,83–85]

Disease	Major genes	Clinical utility
Long QT syndrome	KCNQ1, KCNH2, SCN5A	Confirm diagnosis; avoid genotype-specific triggers for arrhythmias; may affect treatment and risk assessment; can be useful in cascade family screening
Brugada syndrome	SCN5A	Can support diagnosis; may be useful for risk stratification; can be useful in cascade family screening
Catecholaminergic polymorphic ventricular tachycardia	RyR2, CASQ2	Diagnostic criterion; can be useful in cascade family screening
Arrhythmogenic right ventricular cardiomyopathy	PKP2, DSP, DSG2, DSC2, TMEM43	Diagnostic criterion; may consider an arrhythmic risk; can be useful in cascade family screening

KCNQ1, potassium voltage-gated channel subfamily Q member 1; KCNH2, potassium voltage-gated channel subfamily H member 2; SCN5A, sodium voltage-gated channel alpha subunit 5; RyR2, ryanodine receptor 2; CASQ2, calsequestrin 2; PKP2, plakophilin 2; DSP, desmoplakin; DSG2, desmoglein 2; DSC2, desmocollin 2; TMEM43, transmembrane protein 43.

There are few data about whether an asymptomatic carrier of a pathogenic variant needs an ICD. Therefore, current guidelines still do not recommend the genotype-guided ICD as a primary prevention for SCD. However, sophisticated stratification for SCD risk using functional data, such as patch-clamp electrophysiology testing in induced pluripotent stem cells, will be implemented in cardiovascular genetics clinics as part of cascade screening for family members.

CONCLUSIONS

IAs are a group of primary electrical disorders that potentially predispose young individuals, with no evidence of structural heart disease, to SCD. Recent studies have suggested that a substantial proportion of SCD is due to IAs in East Asian people. BrS, LQTS, and IVF constitute the majority of IAs. Patients should be educated to avoid triggers, and an ICD is recommended for secondary prevention. Although each disease may have pathognomonic ECG findings, systemic evaluation is crucial for the diagnosis, and the role of genetic testing is expanding. Advances in genomic sequencing technology will facilitate identification of the underlying genetic pathophysiology of IA syndrome, and will propel physicians into the era of precision medicine in the field of cardiology.