Epidemiology of the inherited cardiomyopathies

WJ McKenna, DP Judge - Nature Reviews Cardiology, 2021 - nature.com
In the absence of contemporary, population-based epidemiological studies, estimates of the
incidence and prevalence of the inherited cardiomyopathies have been derived from …

[HTML][HTML] Cardiac mechanisms of the beneficial effects of SGLT2 inhibitors in heart failure: Evidence for potential off-target effects

JRB Dyck, S Sossalla, N Hamdani, R Coronel… - Journal of molecular and …, 2022 - Elsevier
Sodium glucose cotransporter 2 inhibitors (SGLT2i) constitute a promising drug treatment for
heart failure patients with either preserved or reduced ejection fraction. Whereas SGLT2i …

Cardiac late sodium channel current is a molecular target for the sodium/glucose cotransporter 2 inhibitor empagliflozin

K Philippaert, S Kalyaanamoorthy, M Fatehi, W Long… - Circulation, 2021 - Am Heart Assoc
Background: SGLT2 (sodium/glucose cotransporter 2) inhibitors exert robust
cardioprotective effects against heart failure in patients with diabetes, and there is intense …

Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy

AAM Wilde, AS Amin - JACC: Clinical Electrophysiology, 2018 - jacc.org
SCN5A gene encodes the pore-forming ion-conducting α-subunit of the cardiac sodium
channel (Nav1. 5), which is responsible for the initiation and propagation of action potentials …

The cardiac sodium channel gene SCN5A and its gene product NaV1. 5: Role in physiology and pathophysiology

CC Veerman, AAM Wilde, EM Lodder - Gene, 2015 - Elsevier
The gene SCN5A encodes the main cardiac sodium channel Na V 1.5. This channel
predominates the cardiac sodium current, I Na, which underlies the fast upstroke of the …

SCN5A Variants: Association With Cardiac Disorders

W Li, L Yin, C Shen, K Hu, J Ge, A Sun - Frontiers in physiology, 2018 - frontiersin.org
The SCN5A gene encodes the alpha subunit of the main cardiac sodium channel Nav1. 5.
This channel predominates inward sodium current (INa) and plays a critical role in …

The genetics of Brugada syndrome

M Cerrone, S Costa, M Delmar - Annual review of genomics and …, 2022 - annualreviews.org
Brugada syndrome is a heritable channelopathy characterized by a peculiar
electrocardiogram (ECG) pattern and increased risk of cardiac arrhythmias and sudden …

The electrocardiogram in the diagnosis and management of patients with dilated cardiomyopathy

G Finocchiaro, M Merlo, N Sheikh… - European Journal of …, 2020 - Wiley Online Library
The term dilated cardiomyopathy (DCM) defines a heterogeneous group of cardiac
disorders, which are characterized by left ventricular or biventricular dilatation and systolic …

SCN5A channelopathy: arrhythmia, cardiomyopathy, epilepsy and beyond

CA Remme - … Transactions of the Royal Society B, 2023 - royalsocietypublishing.org
Influx of sodium ions through voltage-gated sodium channels in cardiomyocytes is essential
for proper electrical conduction within the heart. Both acquired conditions associated with …

Human induced pluripotent stem cell–derived cardiomyocytes as models for cardiac channelopathies: a primer for non-electrophysiologists

P Garg, V Garg, R Shrestha, MC Sanguinetti… - Circulation …, 2018 - Am Heart Assoc
Life threatening ventricular arrhythmias leading to sudden cardiac death are a major cause
of morbidity and mortality. In the absence of structural heart disease, these arrhythmias …