Three reasons why iPSC-derived atrial cardiomyocytes are poised to accelerate atrial fibrillation research
Atrial fibrillation is estimated to affect around 6 million people in Europe, making it the most common arrhythmia observed in the clinic. The irregular heartbeat and disturbed electrical activity experienced by atrial fibrillation patients is commonly treated by surgical interventions such as pacemakers or the ablation of diseased tissue, or with non-selective class IC (Nav) and III (Kv) ion channel anti-arrhythmic drugs. However, these approaches can have serious side-effects, so extensive research has been devoted to better understand the cellular mechanisms behind the disease to develop safer and more effective treatments.
Unfortunately, drug discovery efforts underpinned by traditional preclinical animal and non-cardiac cell models of atrial fibrillation have achieved limited success in realising this goal. One major contributing factor is that these systems often do not reliably replicate the physiology of human atrial cardiomyocytes. Alternative models employing human atrial cardiomyocyte primary cells offer more potential. However, the viability and yield of live cells from human hearts is low, and studies can only be performed using limited amounts of material. What’s more, native human tissue typically comes from diseased donors and is often very fibrous – and therefore challenging to work with.
Human induced pluripotent stem cell (iPSC)-derived atrial cardiomyocytes can often be a better solution. They offer a powerful model system for atrial fibrillation drug discovery and disease modelling thanks to three key benefits:
• They provide insights that are more translationally relevant
• They deliver more consistent results
• They are easier to use from a practical standpoint
Here, we consider how each of these advantages is helping to accelerate the delivery of innovative anti-arrhythmic drugs to patients (you can also learn more by downloading our whitepaper on this topic).



