4.6 Review

Sinus node dysfunction: current understanding and future directions

Journal

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00618.2022

Keywords

automaticity; pacemaker; sinus node dysfunction

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The sinoatrial node (SAN) is important for maintaining proper cardiac rhythm and contraction, but abnormalities within it can cause sinus node dysfunction (SND), leading to increased risk of cardiac arrhythmias. Current treatment for SND is limited to pacemaker implantation, but emerging evidence on genetic abnormalities associated with SND may lead to the development of more effective therapies. This review article examines the anatomy and pathophysiology of the SAN, the epidemiology of SND, and discusses the most common genetic mutations correlated with SND, as well as future research and therapeutic opportunities in this field.
The sinoatrial node (SAN) is the primary pacemaker of the heart. Normal SAN function is crucial in maintaining proper cardiac rhythm and contraction. Sinus node dysfunction (SND) is due to abnormalities within the SAN, which can affect the heartbeat fre-quency, regularity, and the propagation of electrical pulses through the cardiac conduction system. As a result, SND often increases the risk of cardiac arrhythmias. SND is most commonly seen as a disease of the elderly given the role of degenerative fibrosis as well as other age-dependent changes in its pathogenesis. Despite the prevalence of SND, current treatment is limited to pacemaker implantation, which is associated with substantial medical costs and complications. Emerging evidence has identi-fied various genetic abnormalities that can cause SND, shedding light on the molecular underpinnings of SND. Identification of these molecular mechanisms and pathways implicated in the pathogenesis of SND is hoped to identify novel therapeutic targets for the development of more effective therapies for this disease. In this review article, we examine the anatomy of the SAN and the pathophysiology and epidemiology of SND. We then discuss in detail the most common genetic mutations correlated with SND and provide our perspectives on future research and therapeutic opportunities in this field.

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