Gene therapy for atrial fibrillation.

J Mol Cell Cardiol

From the Division of Cardiology, University of Massachusetts Medical School, Worcester, MA, United States of America. Electronic address:

Published: November 2024

AI Article Synopsis

  • * Novel therapies, particularly gene therapy, are being explored to address the underlying mechanisms of AF, using specific genes and delivery methods to target structural changes that increase the risk of this arrhythmia.
  • * This review will cover the essential components of gene therapy for AF, including potential molecular targets, methods for delivering genes to the heart, and insights from early testing on effectiveness and safety, while also discussing recent advancements and ongoing challenges in the field.

Article Abstract

Atrial fibrillation (AF) is the most common sustained arrhythmia in adults. Current limitations of pharmacological and ablative therapies motivate the development of novel therapies as next generation treatments for AF. The arrhythmia mechanisms creating and sustaining AF are key elements in the development of this novel treatment. Gene therapy provides a useful platform that allows us to regulate the mechanisms of interest using a suitable transgene(s), vector, and delivery method. Effective gene therapy strategies in the literature have targeted maladaptive electrical or structural remodeling that increase vulnerability to AF. In this review, we will summarize key elements of gene therapy for AF, including molecular targets, gene transfer vectors, atrial gene delivery and preclinical efficacy and toxicity testing. Recent advances and challenges in the field will be also discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11534567PMC
http://dx.doi.org/10.1016/j.yjmcc.2024.09.004DOI Listing

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