Inherited arrhythmias: from gene variants to ionic channel
dysfunctions

p 2022

Inherited arrhythmias: from gene variants to ionic channel dysfunctions

BÉBAROVÁ, Markéta, Olga ŠVECOVÁ, Larisa CHMELÍKOVÁ, Jan HOŠEK, Michal PÁSEK et. al.

Basic information

Original name

Inherited arrhythmias: from gene variants to ionic channel dysfunctions

Authors

BÉBAROVÁ, Markéta (203 Czech Republic, guarantor, belonging to the institution), Olga ŠVECOVÁ (203 Czech Republic, belonging to the institution), Larisa CHMELÍKOVÁ (643 Russian Federation), Jan HOŠEK (203 Czech Republic), Michal PÁSEK (203 Czech Republic, belonging to the institution), Tomáš BÁRTA (203 Czech Republic, belonging to the institution), Jiří PACHERNÍK (203 Czech Republic), Iva SYNKOVÁ (203 Czech Republic, belonging to the institution) and Tomáš NOVOTNÝ (203 Czech Republic, belonging to the institution)

Edition

14th New Frontiers in Basic Cardiovascular Research: France – new EU Members, 2022

Other information

Language

English

Type of outcome

Vyžádané přednášky

Field of Study

30201 Cardiac and Cardiovascular systems

Country of publisher

Slovakia

Confidentiality degree

není předmětem státního či obchodního tajemství

RIV identification code

RIV/00216224:14110/22:00129699

Organization unit

Faculty of Medicine

Keywords in English

Inherited arrhythmia; gene variants; ionic channel dysfunctions

Abstract

V originále

Inherited arrhythmias represent relatively rare, but life-threatening cardiac pathologies. The origin of the arrhythmias is heterogeneous. Variants in genes encoding cardiac ionic channels or associated proteins can be often detected. A complex clinical, genetic, and functional analysis is then needed to reveal if the identified genetic variant may cause the phenotype. The long QT syndrome (LQTS), the most frequent type of inherited arrhythmia, is associated with various genetic variants, most often in the KCNQ1 gene (LQTS type 1, LQT1). This gene encodes the pore-forming subunit (Kv7.1) of slow delayed rectifier K+ (IKs) channels. We have recently characterized IKs dysfunction caused by two LQT1 variants identified in the Czech population, T309I and R562S. T309I resulted in a complete loss of function due to an impaired channel trafficking in the homozygous setting and a dominant-negative effect in the heterozygous setting (representing the situation in heterozygous carriers). R562S showed a preserved channel trafficking and, in the heterozygous setting, haploinsufficiency. The responsiveness to beta-adrenergic stimulation, an important regulator of IKs channel function namely at an increased sympathetic tone (e.g., at exercise), was preserved in T309I channels whereas it was completely missing in R562S channels. Using in silico simulations in the human ventricular cell model, delayed afterdepolarizations were detected as the possible arrhythmogenic mechanism in both variants. Variants in various genes encoding cardiac ionic channels can be also detected in some patients with idiopathic ventricular fibrillation (VF; both structural heart disease and any clinical signs of an inherited arrhythmia are missing). We have recently selected several identified genetic variants in our patients with idiopathic VF for the functional analysis. Patient-specific cardiomyocytes carrying a variant in the RYR2 gene (Y4734C) were prepared and a pilot investigation has been started (patch-clamp and microelectrode array). The first data showed an increased tendency of the patient-specific cardiomyocytes to irregular electric activity at specific conditions (e.g., increased temperature, decreased extracellular K+ concentration, activation of adrenergic receptors). Ongoing detailed analysis is aimed at elucidating the origin of the proarrhythmic activity in the patient. The connection between genotype, clinical phenotype, and subcellular and cellular origin of the dysfunction is relatively clear in the “classic” inherited arrhythmias. In contrast, idiopathic VF is characterized by the absence of any typical clinical phenotype. Hence, ionic channel dysfunction resulting from an identified associated genetic variant is likely masked by compensatory mechanisms and can be revealed only under specific circumstances. Functional analysis of these variants is essential for a better understanding of the pathophysiology of this life-threatening disease.

Links

MUNI/A/1133/2021, interní kód MU

Name: Od buňky k medicíně (Acronym: CELLVIEW)

Investor: Masaryk University

NU22-02-00348, research and development project

Name: Funkční hodnocení genetických variant u případů klinicky „skutečné“ idiopatické fibrilace komor: in vitro a in silico modelování s cílem odhalit arytmogenní mechanismus

Investor: Ministry of Health of the CR, Subprogram 1 - standard

Citovat

BÉBAROVÁ, Markéta, Olga ŠVECOVÁ, Larisa CHMELÍKOVÁ, Jan HOŠEK, Michal PÁSEK, Tomáš BÁRTA, Jiří PACHERNÍK, Iva SYNKOVÁ and Tomáš NOVOTNÝ. Inherited arrhythmias: from gene variants to ionic channel dysfunctions. In 14th New Frontiers in Basic Cardiovascular Research: France – new EU Members. 2022.

@misc{2230912,
   author = {Bébarová, Markéta and Švecová, Olga and Chmelíková, Larisa and Hošek, Jan and Pásek, Michal and Bárta, Tomáš and Pacherník, Jiří and Synková, Iva and Novotný, Tomáš},
   booktitle = {14th New Frontiers in Basic Cardiovascular Research: France – new EU Members},
   keywords = {Inherited arrhythmia; gene variants; ionic channel dysfunctions},
   language = {eng},
   title = {Inherited arrhythmias: from gene variants to ionic channel dysfunctions},
   year = {2022}
}

TY  - SLIDE
ID  - 2230912
AU  - Bébarová, Markéta - Švecová, Olga - Chmelíková, Larisa - Hošek, Jan - Pásek, Michal - Bárta, Tomáš - Pacherník, Jiří - Synková, Iva - Novotný, Tomáš
PY  - 2022
TI  - Inherited arrhythmias: from gene variants to ionic channel dysfunctions
KW  - Inherited arrhythmia
KW  - gene variants
KW  - ionic channel dysfunctions
N2  - Inherited arrhythmias represent relatively rare, but life-threatening cardiac pathologies. The origin of the arrhythmias is heterogeneous. Variants in genes encoding cardiac ionic channels or associated proteins can be often detected. A complex clinical, genetic, and functional analysis is then needed to reveal if the identified genetic variant may cause the phenotype. The long QT syndrome (LQTS), the most frequent type of inherited arrhythmia, is associated with various genetic variants, most often in the KCNQ1 gene (LQTS type 1, LQT1). This gene encodes the pore-forming subunit (Kv7.1) of slow delayed rectifier K+ (IKs) channels. We have recently characterized IKs dysfunction caused by two LQT1 variants identified in the Czech population, T309I and R562S. T309I resulted in a complete loss of function due to an impaired channel trafficking in the homozygous setting and a dominant-negative effect in the heterozygous setting (representing the situation in heterozygous carriers). R562S showed a preserved channel trafficking and, in the heterozygous setting, haploinsufficiency. The responsiveness to beta-adrenergic stimulation, an important regulator of IKs channel function namely at an increased sympathetic tone (e.g., at exercise), was preserved in T309I channels whereas it was completely missing in R562S channels. Using in silico simulations in the human ventricular cell model, delayed afterdepolarizations were detected as the possible arrhythmogenic mechanism in both variants. Variants in various genes encoding cardiac ionic channels can be also detected in some patients with idiopathic ventricular fibrillation (VF; both structural heart disease and any clinical signs of an inherited arrhythmia are missing). We have recently selected several identified genetic variants in our patients with idiopathic VF for the functional analysis. Patient-specific cardiomyocytes carrying a variant in the RYR2 gene (Y4734C) were prepared and a pilot investigation has been started (patch-clamp and microelectrode array). The first data showed an increased tendency of the patient-specific cardiomyocytes to irregular electric activity at specific conditions (e.g., increased temperature, decreased extracellular K+ concentration, activation of adrenergic receptors). Ongoing detailed analysis is aimed at elucidating the origin of the proarrhythmic activity in the patient. The connection between genotype, clinical phenotype, and subcellular and cellular origin of the dysfunction is relatively clear in the “classic” inherited arrhythmias. In contrast, idiopathic VF is characterized by the absence of any typical clinical phenotype. Hence, ionic channel dysfunction resulting from an identified associated genetic variant is likely masked by compensatory mechanisms and can be revealed only under specific circumstances. Functional analysis of these variants is essential for a better understanding of the pathophysiology of this life-threatening disease.
ER  -

BÉBAROVÁ, Markéta, Olga ŠVECOVÁ, Larisa CHMELÍKOVÁ, Jan HOŠEK, Michal PÁSEK, Tomáš BÁRTA, Jiří PACHERNÍK, Iva SYNKOVÁ and Tomáš NOVOTNÝ. Inherited arrhythmias: from gene variants to ionic channel dysfunctions. In \textit{14th New Frontiers in Basic Cardiovascular Research: France – new EU Members}. 2022.

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