Atrial fibrillation ablation in patients with arrhythmia‐induced cardiomyopathy: a prospective multicentre study

Author:

González‐Ferrero Teba123ORCID,Bergonti Marco456,López‐Canoa José Nicolás37,Arias Federico García‐Rodeja123,Eiras Penas Sonia23,Spera Francesco45,González‐Maestro Adrián2,Minguito‐Carazo Carlos123,Martínez‐Sande José Luis123,González‐Melchor Laila123,García‐Seara Francisco Javier123,Fernández‐López Jesús Alberto123,Álvarez‐Castro Ezequiel23,González‐Juanatey José Ramón123,Heidbuchel Hein45,Sarkozy Andrea45,Rodríguez‐Mañero Moisés123

Affiliation:

1. Cardiovascular Area and Coronary Unit University Clinical Hospital of Santiago de Compostela Santiago de Compostela Spain

2. Translational Cardiology Group, Health Research Institute of Santiago de Compostela (IDIS) University Clinical Hospital of Santiago de Compostela Travesía da Choupana s/n Santiago de Compostela 15706 A Coruña Spain

3. CIBERCV Carlos III Health Institute Madrid Spain

4. Department of Cardiology Antwerp University Hospital Antwerp Belgium

5. Cardiovascular Research, GENCOR University of Antwerp Antwerp Belgium

6. Division of Cardiology, Cardiocentro Ticino Institute Ente Ospedaliero Cantonale Lugano Switzerland

7. Department of Cardiology University Hospital Complex of Pontevedra Pontevedra Spain

Abstract

AbstractAimsThis study aims to investigate the clinical and biochemical characteristics of patients with atrial fibrillation (AF) referred for ablation who develop arrhythmia‐induced cardiomyopathy (AiCM) as well as their long‐term outcomes after catheter ablation (CA).Methods and resultsA prospective multicentre study was conducted on consecutive AF patients who underwent CA. AiCM was defined as the development of heart failure in the presence of AF and an improvement of left ventricular fraction by at least 10% at 6 months after ablation. A subgroup of patients underwent peripheral and left atrial blood samples [galectin‐3, fatty acid‐binding protein 4 (FABP4), and soluble receptor for advanced glycation end products (sRAGE)] at the time of the procedure. Of the 769 patients who underwent AF ablation, 135 (17.56%) met the criteria for AiCM. Independent predictors of AiCM included persistent AF, male gender, left atrial volume, QRS width, active smoking, and chronic kidney disease (CKD). Biomarker analysis revealed that sRAGE, FABP4, and galectin‐3 levels were not predictive of AiCM development nor did they differ between groups or predict recurrence. There were no differences in AF recurrence between patients with and without AiCM (30.83% vs. 27.77%; P = 0.392) during a median follow‐up of 23.83 months (inter‐quartile range 9–36).ConclusionsIn the subset of patients referred for AF ablation, the development of AiCM was associated with persistent AF and CKD. Biomarker analysis was not different between groups nor predicted recurrence. Patients with AiCM benefited from ablation, with a significant improvement in left ventricular ejection fraction and similar AF recurrence rates to those without AiCM.

Funder

Instituto de Salud Carlos III

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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