Language

English

Publication Date

5-1-2024

Journal

Expert Opinion on Therapeutic Targets

DOI

10.1080/14728222.2024.2351501

PMID

38700451

PMCID

PMC11395937

PubMedCentral® Posted Date

5-13-2025

PubMedCentral® Full Text Version

Author MSS

Abstract

Introduction: The cardiac conduction system (CCS) is crucial for maintaining adequate cardiac frequency at rest and modulation during exercise. Furthermore, the atrioventricular node and His-Purkinje system are essential for maintaining atrioventricular and interventricular synchrony and consequently maintaining an adequate cardiac output.

Areas covered: In this review article, we examine the anatomy, physiology, and pathophysiology of the CCS. We then discuss in detail the most common genetic mutations and the molecular mechanisms of cardiac conduction disease (CCD) and provide our perspectives on future research and therapeutic opportunities in this field.

Expert opinion: Significant advancement has been made in understanding the molecular mechanisms of CCD, including the recognition of the heterogeneous signaling at the subcellular levels of sinoatrial node, the involvement of inflammatory and autoimmune mechanisms, and the potential impact of epigenetic regulations on CCD. However, the current treatment of CCD manifested as bradycardia still relies primarily on cardiovascular implantable electronic devices (CIEDs). On the other hand, an If specific inhibitor was developed to treat inappropriate sinus tachycardia and sinus tachycardia in heart failure patients with reduced ejection fraction. More work is needed to translate current knowledge into pharmacologic or genetic interventions for the management of CCDs.

Keywords

Humans, Animals, Heart Conduction System, Cardiac Conduction System Disease, Molecular Targeted Therapy, Mutation, Drug Development, Heart Failure, Epigenesis, Genetic, Sinoatrial Node, cardiac conduction disease, pacemaker, sinoatrial node, atrioventricular node, His-Purkinje System

Published Open-Access

yes

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