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Identifying Atrial Fibrillation Mechanisms for Personalized Medicine

Atrial fibrillation (AF) is a major cause of heart failure and stroke. The early maintenance of sinus rhythm has been shown to reduce major cardiovascular endpoints, yet is difficult to achieve. For instance, it is unclear how discoveries at the genetic and cellular level can be used to tailor pharm...

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Detalles Bibliográficos
Autores principales: Deb, Brototo, Ganesan, Prasanth, Feng, Ruibin, Narayan, Sanjiv M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658178/
https://www.ncbi.nlm.nih.gov/pubmed/34884381
http://dx.doi.org/10.3390/jcm10235679
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author Deb, Brototo
Ganesan, Prasanth
Feng, Ruibin
Narayan, Sanjiv M.
author_facet Deb, Brototo
Ganesan, Prasanth
Feng, Ruibin
Narayan, Sanjiv M.
author_sort Deb, Brototo
collection PubMed
description Atrial fibrillation (AF) is a major cause of heart failure and stroke. The early maintenance of sinus rhythm has been shown to reduce major cardiovascular endpoints, yet is difficult to achieve. For instance, it is unclear how discoveries at the genetic and cellular level can be used to tailor pharmacotherapy. For non-pharmacologic therapy, pulmonary vein isolation (PVI) remains the cornerstone of rhythm control, yet has suboptimal success. Improving these therapies will likely require a multifaceted approach that personalizes therapy based on mechanisms measured in individuals across biological scales. We review AF mechanisms from cell-to-organ-to-patient from this perspective of personalized medicine, linking them to potential clinical indices and biomarkers, and discuss how these data could influence therapy. We conclude by describing approaches to improve ablation, including the emergence of several mapping systems that are in use today.
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spelling pubmed-86581782021-12-10 Identifying Atrial Fibrillation Mechanisms for Personalized Medicine Deb, Brototo Ganesan, Prasanth Feng, Ruibin Narayan, Sanjiv M. J Clin Med Review Atrial fibrillation (AF) is a major cause of heart failure and stroke. The early maintenance of sinus rhythm has been shown to reduce major cardiovascular endpoints, yet is difficult to achieve. For instance, it is unclear how discoveries at the genetic and cellular level can be used to tailor pharmacotherapy. For non-pharmacologic therapy, pulmonary vein isolation (PVI) remains the cornerstone of rhythm control, yet has suboptimal success. Improving these therapies will likely require a multifaceted approach that personalizes therapy based on mechanisms measured in individuals across biological scales. We review AF mechanisms from cell-to-organ-to-patient from this perspective of personalized medicine, linking them to potential clinical indices and biomarkers, and discuss how these data could influence therapy. We conclude by describing approaches to improve ablation, including the emergence of several mapping systems that are in use today. MDPI 2021-12-01 /pmc/articles/PMC8658178/ /pubmed/34884381 http://dx.doi.org/10.3390/jcm10235679 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Deb, Brototo
Ganesan, Prasanth
Feng, Ruibin
Narayan, Sanjiv M.
Identifying Atrial Fibrillation Mechanisms for Personalized Medicine
title Identifying Atrial Fibrillation Mechanisms for Personalized Medicine
title_full Identifying Atrial Fibrillation Mechanisms for Personalized Medicine
title_fullStr Identifying Atrial Fibrillation Mechanisms for Personalized Medicine
title_full_unstemmed Identifying Atrial Fibrillation Mechanisms for Personalized Medicine
title_short Identifying Atrial Fibrillation Mechanisms for Personalized Medicine
title_sort identifying atrial fibrillation mechanisms for personalized medicine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658178/
https://www.ncbi.nlm.nih.gov/pubmed/34884381
http://dx.doi.org/10.3390/jcm10235679
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