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Updated: Apr 11, 2026

Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Atrial fibrillation in hypertrophic cardiomyopathy: A unique clinical entity requiring dedicated study
Ethan J Rowin1, Konstantinos C Siontis2, Anjali Owens3
1Hypertrophic Cardiomyopathy Center, Lahey Hospital and Medical Center, Burlington, Massachusetts.
Insights
Atrial fibrillation in hypertrophic cardiomyopathy (HCM-AF) is a distinct condition. Current therapies for non-HCM atrial fibrillation (AF) show limited success in HCM-AF patients, necessitating dedicated research.
Area of Science:
- Cardiology
- Electrophysiology
- Genetics
Background:
- Atrial fibrillation (AF) is common in hypertrophic cardiomyopathy (HCM), affecting 20-25% of patients.
- HCM-AF is linked to increased stroke risk and heart failure.
- Disease-specific mechanisms in HCM-AF include atrial remodeling and dysfunction, creating an atrial myopathy.
Purpose of the Study:
- To establish atrial fibrillation in hypertrophic cardiomyopathy (HCM-AF) as a distinct clinical entity.
- To highlight knowledge and care gaps in managing HCM-AF.
- To emphasize the need for dedicated research into HCM-AF therapeutics.
Main Methods:
- Review of current literature on AF in HCM.
- Analysis of disease-specific mechanisms differentiating HCM-AF from non-HCM AF.
- Comparison of therapeutic outcomes between HCM-AF and non-HCM AF populations.
Main Results:
- HCM-AF arises from unique pathophysiological processes distinct from non-HCM AF.
- Contemporary AF therapies yield poorer outcomes in HCM-AF compared to non-HCM AF.
- Lower success rates for rhythm control via catheter ablation and antiarrhythmic drugs in HCM-AF.
Conclusions:
- HCM-AF is a unique clinical entity requiring specialized investigation.
- Current therapeutic strategies for AF may not be directly transferable to HCM-AF patients.
- Further research is crucial to develop effective treatments for HCM-AF.
Abstract:
Atrial fibrillation (AF) is the most common sustained arrhythmia in hypertrophic cardiomyopathy (HCM) occurring in 20%-25% of patients and associated with significant morbidity including stroke risk and worsening heart failure. AF in HCM (HCM-AF) arises from disease-specific mechanisms distinct from non-HCM-AF, including HCM-related atrial structural changes (dilation/fibrosis), biophysical abnormalities (within ion-channels), and atrial dysfunction that culminate in an HCM-specific atrial myopathy. Although the adoption of contemporary AF therapies have been associated with improved clinical outcomes in non-HCM-AF populations, outcomes in HCM-AF remain worse, including lower rates of rhythm control success with catheter ablation and antiarrhythmic medications. In this context, we provide support that HCM-AF is a distinct clinical entity, highlighting gaps in knowledge and care, and represents an area of need for dedicated investigation as the effectiveness of applying therapeutics from AF populations without HCM to populations with HCM is unclear.
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