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Updated: Mar 17, 2026

Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Toward a Prospective Definition of Atrial Fibrillation-induced Cardiomyopathy
Nikhil Ahluwalia1,2, Shohreh Honarbakhsh1,2, Ross J Hunter1,2
1St Bartholomew's Hospital London, UK.
Insights
Atrial fibrillation (AF) can cause left ventricular systolic dysfunction (LVSD) through various mechanisms. A new marker, the Restitution Threshold Index (RTI), may help identify patients needing rhythm control for AF-induced cardiomyopathy (AIC).
Area of Science:
- Cardiology
- Electrophysiology
- Cardiomyopathy Research
Background:
- Atrial fibrillation (AF) is a common arrhythmia linked to left ventricular systolic dysfunction (LVSD).
- AF-induced cardiomyopathy (AIC) involves complex mechanisms beyond just rapid heart rates, necessitating distinct diagnostic and therapeutic approaches.
- Current diagnostic methods for AIC are retrospective, limiting proactive clinical management.
Purpose of the Study:
- To review the multifaceted mechanisms by which AF contributes to LVSD.
- To explore advanced imaging parameters and novel markers for prospectively identifying AIC.
- To discuss the potential of integrating new markers with existing imaging techniques for improved clinical decision-making.
Main Methods:
- Narrative review of existing literature on AF and its impact on ventricular function.
- Discussion of established and emerging imaging modalities (e.g., cardiac MRI, stress echocardiography) for assessing LVSD.
- Introduction and review of the Restitution Threshold Index (RTI) as a novel marker for AF-related ventricular dysfunction.
Main Results:
- AF impairs ventricular function through rapid rate, rhythm irregularity, and impaired atrial contraction, often exploiting underlying structural vulnerabilities.
- Existing imaging parameters like late gadolinium enhancement and contractile reserve offer insights but have limitations.
- The Restitution Threshold Index (RTI) is proposed as a non-parametric marker that considers both ventricular rate and AF's irregularity.
Conclusions:
- Identifying specific mechanisms of AIC is challenging but crucial for effective treatment.
- Integrating the novel RTI marker with imaging-based parameters may improve the prospective identification of patients who would benefit from rhythm control therapies.
- Further validation of RTI is essential for developing accessible clinical tools, with an open-access calculator now available.
Abstract:
AF can mediate left ventricular systolic dysfunction (LVSD) through a tachycardia-mediated cardiomyopathic process that may reverse with rate control alone. However, additional mechanisms contribute to AF-induced cardiomyopathy (AIC) that require rhythm control therapies. AIC can currently only be diagnosed retrospectively, as these component mechanisms are difficult to distinguish from each other and from other causes of LVSD prospectively. This narrative review considers the different potential mechanisms through which AF can impair ventricular function: rapid ventricular rate; irregularity of the ventricular rhythm; and impaired atrial contraction. How these features may exploit underlying structural vulnerability are considered and additional imaging-based parameters such as late gadolinium enhancement on cardiac MRI and contractile reserve during stress echocardiography are discussed. The limitations of existing parameters are discussed and a novel, non-parametric marker of ventricular rate with consideration of the inherent irregularity of AF - the Restitution Threshold Index (RTI) - is reviewed. Integrating RTI with these imaging-based measures may enhance clinical decision-making by more accurately identifying patients who would benefit from timely rhythm control. Further prospective validation is essential to develop accessible tools and an open-access RTI calculator has been made available (https://restitutionthreshold.com) to facilitate reproducibility and wider application.
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