Towards Improved Human In Vitro Models for Cardiac Arrhythmia: Disease Mechanisms, Treatment, and Models of Atrial Fibrillation

Author:

Cofiño-Fabres Carla1ORCID,Passier Robert12ORCID,Schwach Verena1ORCID

Affiliation:

1. Department of Applied Stem Cell Technologies, TechMed Centre, University of Twente, Drienerlolaan 5, 7500 AE Enschede, The Netherlands

2. Department of Anatomy and Embryology, Leiden University Medical Centre, 2300 RC Leiden, The Netherlands

Abstract

Heart rhythm disorders, arrhythmias, place a huge economic burden on society and have a large impact on the quality of life of a vast number of people. Arrhythmias can have genetic causes but primarily arise from heart tissue remodeling during aging or heart disease. As current therapies do not address the causes of arrhythmias but only manage the symptoms, it is of paramount importance to generate innovative test models and platforms for gaining knowledge about the underlying disease mechanisms which are compatible with drug screening. In this review, we outline the most important features of atrial fibrillation (AFib), the most common cardiac arrhythmia. We will discuss the epidemiology, risk factors, underlying causes, and present therapies of AFib, as well as the shortcomings and opportunities of current models for cardiac arrhythmia, including animal models, in silico and in vitro models utilizing human pluripotent stem cell (hPSC)-derived cardiomyocytes.

Funder

Hartstichting

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

Reference136 articles.

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2. Atrial fibrillation;Lip;Nat. Rev. Dis. Prim.,2016

3. Cellular and molecular electrophysiology of atrial fibrillation initiation, maintenance, and progression;Heijman;Circ. Res.,2014

4. Asymptomatic atrial fibrillation: Demographic features and prognostic information from the Atrial Fibrillation Follow-up Investigation of Rhythm Management (AFFIRM) study;Flaker;Am. Heart J.,2005

5. Worldwide Epidemiology of Atrial Fibrillation: A Global Burden of Disease 2010 Study;Chugh;Circulation,2014

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