|Year : 2021 | Volume
| Issue : 4 | Page : 339-344
Calmodulinopathy in inherited arrhythmia syndromes
Wen-Chin Tsai1, Peng-Sheng Chen2, Michael Rubart3
1 Department of Cardiology, Cardiovascular Research Center, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, and Tzu Chi University, Hualien, Taiwan
2 Department of Cardiology, Cedar-Sinai Medical Center, Los Angeles, CA; Krannert Institute of Cardiology, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA
3 Krannert Institute of Cardiology, Department of Medicine; Department of Pediatrics, Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA
|Date of Submission||21-Jul-2020|
|Date of Decision||02-Sep-2020|
|Date of Acceptance||07-Oct-2020|
|Date of Web Publication||14-Apr-2021|
Department of Pediatrics, Wells Center for Pediatric Research, Indiana University School of Medicine, 1044 West Walnut Street, Indianapolis, IN 46202
Source of Support: None, Conflict of Interest: None
Calmodulin (CaM) is a ubiquitous intracellular calcium sensor that controls and regulates key cellular functions. In all vertebrates, three CaM genes located on separate chromosomes encode an identical 149 amino acid protein, implying an extraordinarily high level of evolutionary importance and suggesting that CaM mutations would be possibly fatal. Inherited arrhythmia syndromes comprise a spectrum of primary electrical disorders caused by mutations in genes encoding ion channels or associated proteins leading to various cardiac arrhythmias, unexplained syncope, and sudden cardiac death. CaM mutations have emerged as an independent entity among inherited arrhythmia syndromes, referred to as calmodulinopathies. The most common clinical presentation associated with calmodulinopathy is congenital long QT syndrome, followed by catecholaminergic polymorphic ventricular tachycardia, both of which significantly increase the possibility of repeated syncope, lethal arrhythmic events, and sudden cardiac death, especially in young individuals. Here, we aim to give an overview of biochemical and structural characteristics of CaM and progress toward updating current known CaM mutations and associated clinical phenotypes. We also review the possible mechanisms underlying calmodulinopathy, based on several key in vitro studies. We expect that further experimental studies are needed to explore the complexity of calmodulinopathy.
Keywords: Calmodulinopathy, Catecholaminergic polymorphic ventricular tachycardia, Long QT syndrome and inherited arrhythmia syndromes
|How to cite this article:|
Tsai WC, Chen PS, Rubart M. Calmodulinopathy in inherited arrhythmia syndromes. Tzu Chi Med J 2021;33:339-44
| Introduction|| |
Calcium ions (Ca2+) influence nearly every aspect of cellular life. Calmodulin (CaM), a ubiquitously expressed Ca2+-binding protein, has a vital role in relaying Ca2+ signals into biochemical and biomechanical responses by altering protein–protein interactions. As a result, CaM regulates a wide spectrum of cellular functions, including metabolism, gene expression, proliferation, contraction, and proteolysis. No other molecule highlights the evolutionary importance of Ca2+ signaling. Although the properties and biological functions of CaM have been widely studied since its early discovery by Cheung in 1970, there are still considerable knowledge gaps that limit our understanding of Ca2+/CaM interactions with and the identity of its target proteins.
Inherited arrhythmia syndromes are electrical abnormalities of the heart caused by mutations in genes encoding cardiac ion channels or associated proteins. Unfortunately, sudden cardiac death, an unexpected natural death, might be the first clinical presentation in patients with inherited arrhythmia syndrome, especially in young adolescence. Arrhythmia syndromes may manifest as catecholaminergic polymorphic ventricular tachycardia (CPVT) and/or long QT syndrome (LQTS). The first arrhythmogenic CaM mutation was identified in a large Swedish family with severe and inherited CPVT, causing syncope and sudden death. Since then, more and more CaM mutations have been identified in patients, especially in young individuals, presenting with CPVT and/or LQTS.
Calmodulinopathy has emerged as another life-threatening, inherited arrhythmia syndrome. We summarize currently available knowledge on inherited arrhythmia syndromes. Specifically, we focus on this severe arrhythmogenic syndrome, termed calmodulinopathy, and also review CaM-encoding genes, protein structure and function, as well as the spectrum of CaM mutations and their associated phenotypes. Finally, we review the possible mechanisms underlying this complex arrhythmia syndrome.
| Calmodulin Genes, Structure, and Function|| |
CaM is a small, ubiquitous adaptor protein that transduces Ca2+ signals into activities of downstream effector proteins. Three different CaM genes (CALM1, CALM2, and CALM3), located on three different chromosomes (14q32.11, 2p21, and 19q13.32, respectively), encode an identical, 149 amino acid protein. CaM consists of an N- and a C-lobe, connected by an α-helix linker. Each lobe contains two EF-hand motifs, each one binding one Ca2+ ion. Thus, CaM can bind up to 4 Ca2+ ions with dissociation constants (KD) ranging from 1 to 10 μM. Calcium binding changes CaM conformation, exposing a methionine-rich hydrophobic patch, at either N- or C-lobe, suitable for peptide binding sequences in its target molecules. Intriguingly, the evolutionary significance of CaM is emphasized not only by the appearance of three different genes in three different chromosomes but also by the highly conserved protein sequence across all vertebrates. CaM in both its Ca2+-free (Apo-CaM) and Ca2+-bound form (Ca2+-CaM) significantly impacts on ion homeostasis of cardiomyocytes. Excitation contraction coupling is the process linking electrical excitation to contraction. Pacemaker cells undertake spontaneous depolarization and generate propagating action potentials, which lead to coordinated contraction of the heart. CaM modulates cardiac action potential through modulation of ion channel gating, including cardiac sodium, calcium, and potassium channels. Furthermore, CaM acting as an essential Ca2+ sensor interacts with multiple key downstream proteins by modulating Ca2+ influx, sarcoplasmic reticulum Ca2+ release, and Ca2+ recycling during cardiac excitation–contraction coupling. Therefore, CaM gene mutations result in dysfunction of cardiac ion channels, leading to arrhythmias.
| Inherited Arrhythmia Syndromes|| |
Inherited arrhythmia syndromes manifest as long and short QT syndrome, Brugada syndrome, CPVT, and early repolarization syndrome. [Table 1] lists prevalence, electrocardiographic characteristics, underlying gene mutation, sex preference, age of onset, and known triggers for each type of congenital arrhythmia syndromes. The majority of inherited arrhythmia syndrome present with a disease-specific electrocardiogram (ECG) phenotype, demarcated by abnormal depolarization and/or repolarization, such as the coved-type ST-segment elevation in the right precordial leads, J-point elevation in inferolateral leads, and long QT and short QT intervals [Table 1]. These genetic abnormalities, implying altered imbalance in cardiac ion channel activities, provide an arrhythmogenic substrate that increases the risk of developing ventricular arrhythmias and subsequent sudden cardiac death, often in young individuals. With the recent advance in genetic testing, disease-causing genes for inherited arrhythmias have been successfully mapped, which has a great advantage in individualized patient care. Genetic testing in a proband or linkage mapping in affected family members is highly valuable in the diagnosis of inherited arrhythmia syndromes. The LQTS is the best example for correlation between a certain mutation (genotype) and clinical presentation (phenotypes). CaM mutation-related inherited arrhythmias have been discovered in patients with a severe cardiac phenotype, characterized by a high penetrance, thus postulating a high propensity to lethal ventricular arrhythmias, syncope, and sudden cardiac death at a young age.
| Reported Inherited Arrhythmia Syndromes Associated With Calmodulinopathy|| |
Inherited arrhythmia syndromes are found in more than half of unexplained cases of sudden cardiac death in young persons. Although the incidence is low, an early diagnosis helps initiating therapies to reduce the risk of sudden cardiac death. In 2012, Nyegaard and colleagues first identified two unrelated, de novo missense mutations (p. Asn54Ile; p. Asn98Ser) in the CALM1 gene (start methionine denoted residue 1), leading to the development of early-onset CPVT or CPVT-like arrhythmia. In 2013, Crotti et al. discovered three heterozygous de novo mutations in either CALM1 (p. Asp130Gln; p. Phe142 Leu) or CALM2 (p. Asp96Val) genes, presenting with recurrent cardiac arrest and dramatically prolonged QTc interval. Since then, more mutations in the CaM-encoding genes CALM1, CALM2, and CALM3 have been reported and linked to ventricular arrhythmias manifesting with features of CPVT and/or LQTS,,,,,,,,,.
CPVT is an inherited arrhythmia syndrome, characterized by a normal resting ECG and polymorphic ventricular tachycardia induced by exercise or emotional stress in the absence of structural heart disease. Patients typically experience episodes of syncope and even sudden cardiac death, especially in young individuals. If untreated, the disease is highly lethal, as approximately 30% of those affected experience at least one cardiac arrest and up to 80% one or more syncopal spells. Heterozygosity for mutations in the ryanodine receptor 2 gene (RYR2 [MIM 180902], CPVT1), or calsequestrin-2 gene (CASQ2 [MIM114251], CPVT2) is known to cause the autosomal dominant inheritance pattern of CPVT. CALM1 and CALM2 mutations associated with CPVT were named CPVT4. Beta-blockers are considered first-line therapy, but unfortunately, they are not entirely effective in preventing life-threatening arrhythmias. A cardioverter–defibrillator is often implanted in patients who continue to have ventricular arrhythmias despite beta-blocker therapy. Other anti-arrhythmic agents, including flecainide and Ca2+ channel blockers, have also been used successfully in some cases. Small-scale studies show that left sympathetic ganglionectomy is effective in patients who are insufficiently protected by beta-blocker therapy and/or experience repeated electrical shocks from implanted defibrillators.
The congenital LQTS is a primary cardiac electrical disease, characterized by a prolongation of the QT interval on the ECG and by the manifestation of unexplained syncope or even cardiac arrest, mainly triggered by emotional or physical stress. The QT interval reflects the duration of the ventricular action potential, which is determined by the function of different ion channels. Mutations in KCNQ1 (LQT1, voltage-gated potassium channel), KCNH2 (LQT2, voltage-gated potassium channel), and SCN5A (LQT3, voltage-gated sodium channel) account for at least 75% of congenital LQTS,. LQTSs caused by mutations in CALM1, 2, and 3 genes are categorized as LQT 14, 15, and 16, respectively. In symptomatic, untreated LQT patients, mortality is very high, reaching 21% within one year after the first syncopal episode. In sharp contrast, with proper treatment, mortality is less than 1% during a 15-year follow-up, which makes the existence of symptomatic but undiagnosed patients unacceptable. Lifestyle modification, beta-blockers, left cardiac sympathetic denervation, and implantable cardioverter-defibrillator are the most important therapeutic modalities in the proper management of LQTS patients.
[Table 2] lists arrhythmia syndromes associated with CaM mutations. Most patients develop symptoms in early life, even at the gestational stage. LQTS seems to be the dominant phenotype. By far, there is no overt sex or race prevalence. The functional consequences of the CaM mutations appear to be sufficiently severe to override any influence on the phenotype by the racial or gender background. Interestingly, carriers of the p. N98S, p. D132E, and p. Q132P CaM mutations displayed combined arrhythmia syndromes of CPVT and LQTS.
|Table 2: List of published calmodulin mutations-related inherited arrhythmia syndromes|
Click here to view
In line with the most extensive International Calmodulinopathy Registry, among 74 subjects carrying a pathogenic CaM mutation, 35 single-nucleotide substitutions were identified in the 74 CALM-positive patients (36 CALM1, 23 CALM2, and 15 CALM3 patients) using whole-exome sequencing, targeted next-generation sequencing, or Sanger sequencing. These 35 variants occurred similarly among 3 CALM genes. Sixty-four (86.5%) were symptomatic, and the 10-year cumulative mortality was 27%. The predominant phenotype is LQTS (49%), followed by CPVT (28%). LQTS patients have high incidences of life-threatening arrhythmias (78%) with a median onset age of 1.5 years and poor response to therapies. The ECG pattern resembles that of LQTS type 3, which had a worse prognosis when compared to LQTS type 1 and type 2. All CPVT patients were symptomatic with a median onset age of 6.0 years, and 48% of which presented with major arrhythmic events. The registry discovered another combined phenotype, p. D134N. Undoubtedly, calmodulinopathy has become one of the main disease entities among patients with inherited arrhythmia syndromes.
| Underlying Mechanisms of Calmodulinopathies|| |
Dysregulation of Ca2+ entry into the cytosol of cardiomyocytes has been proposed as the primary mechanism of arrhythmias associated with CaM mutations, either resulting from increased Ca2+ entry through inactivation-incompetent L-type Ca2+ channels (CaV1.2) or from increased SR Ca2+ release via disinhibited cardiac ryanodine receptors (RyR2),,.
Several in vitro studies have proven that RyR2 and CASQ2 gene mutations lead to an increased diastolic leakage of Ca2+ from the sarcoplasmic reticulum of ventricular cardiomyocytes, particularly under adrenergic stimulation, promoting delayed afterdepolarization-induced triggered activities,. CaM physiologically inhibits RyR2 activity. The CPVT-associated CaM mutations p. N54I, p. N98S, and p. A103V all showed RyR2 disinhibition and, therefore, augmented RyR2 opening probability leading to Ca2+ waves, which in turn may cause delayed afterdepolarizations [Table 3]. However, it has remained unclear whether CaM mutation-induced RyR2 dysfunction underlies CPVT in vivo.
The properties of CaV1.2 control cardiac action potential generation, morphology, and duration. Furthermore, CaV1.2 plays the primary role in providing Ca2+ for the initiation of Ca2+-induced Ca2+ release in cardiac myocytes. During the repolarization phase, Ca2+-dependent inactivation (CDI) of CaV1.2 limits Ca2+ entry under physiological conditions, and disruption of this vital feedback mechanism is known to result in severe LQTS. For example, LQTS 8, known as Timothy syndrome, is associated with severe defects in CDI. Correspondingly, loss of CDI was observed for several LQTS-causing CaM mutations, including p. D96V, p. D130G, p. E141G, and p. F142 L. So far, all patients with calmodulinopathy only harbor a mutation in 1 out of 6 CaM-encoding alleles. Taking advantages of using induced pluripotent stem cell-derived cardiomyocytes from LQTS patients heterozygous for mutations in one CaM gene (CALM1-F142 L; CALM2-N98S/D130G), several recent studies have demonstrated a strong dominant-negative effect of single-mutant CaM alleles on CDI of CaV1.2, resulting in prolonged action potential duration, which could be rescued by selectively knocking out the mutant gene while sparing the wild-type counterparts,,.
The detailed mechanisms of how a mutation in one of the six alleles leads to such severe arrhythmia syndromes remain unclear. There is a complex genotype–phenotype correlation. Generally speaking, the magnitude of Ca2+ affinity reduction correlated with the severity of CDI impairment of CaV1.2, which in turn would decide the amplitude of action potential prolongation and believed to be a major cause of LQTS. On the other hand, dysfunctional RyR-mediated Ca2+ handling has been implicated in the pathogenesis of cardiac arrhythmias, especially in established CPVT mouse model and documented human CPVT. Ca2+ leak through RyR can cause triggered activity in the form of delayed afterdepolarizations, which have the propensity to evoke a premature beat to initiate the arrhythmia. In addition, in vitro studies had proved that Purkinje cells are critical contributors to arrhythmic triggers in established mouse models of CPVT, which might implicate the possible role of Purkinje fiber in the calmodulinopathy,. However, the effect of CaM mutation on the function RyR2 is more complex and not directly linked to Ca2+ affinity. For example, the phosphorylation of RyR2 and subsequent sarcoplasmic reticulum Ca2+ release is dependent on Ca2+/CaM-dependent kinase II, which adds an additional layer of complexity when trying to understanding the pathogenesis. As for those carriers, displaying the phenotypes of either CPVT, LQTS, or both, environmental factors or modifier genes might also have an influence on the clinical manifestation.
| Conclusion|| |
Since the first case of CaM mutation-associated CPVT was identified in 2012, calmodulinopathies have emerged as a novel cause of human inherited arrhythmia syndromes. Thus far, approximately 30 CaM mutations with clear disease association have been recognized. A better understanding of the fundamental mechanisms is mandatory. Several in vitro biochemical, as well as cellular studies, have demonstrated that particularly, the regulation of the CaV1.2 and RyR2 is affected by these mutations. We have developed the first knock-in mouse model, heterozygous for the p. N98S mutation in Calm1, which presents with an overlap of CPVT and LQTS,. Future studies using this novel mouse model should have a great value for unraveling calmodulinopathy mechanisms as well as the possible treatment options for patients suffering from CaM-associated inherited arrhythmia syndromes.
Financial support and sponsorship
The work was supported by the grant of Buddhist Tzu Chi Medical Foundation (TCMMP 109-01).
Conflicts of interest
There are no conflicts of interest.
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[Table 1], [Table 2], [Table 3]