Journal
JACC-CLINICAL ELECTROPHYSIOLOGY
Volume 4, Issue 8, Pages 999-1007Publisher
ELSEVIER
DOI: 10.1016/j.jacep.2018.04.013
Keywords
atrial fibrillation; cardiac MRI; catheter ablation; diffuse fibrosis; systolic dysfunction
Categories
Funding
- Baker Heart and Diabetes Institute
- National Health and Medical Research Council (NHMRC) of Australia
- National Heart Foundation of Australia
- NHMRC
- Victorian Government's Operational Infrastructure Funding
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OBJECTIVES This study sought to determine if diffuse ventricular fibrosis improves in patients with atrial fibrillation (AF)-mediated cardiomyopathy following the restoration of sinus rhythm. BACKGROUND AF coexists in 30% of heart failure (HF) patients and may be an underrecognized reversible cause of left ventricular systolic dysfunction. Myocardial fibrosis is the hallmark of adverse cardiac remodeling in HF, yet its reversibility is unclear. METHODS Patients with persistent AF and an idiopathic cardiomyopathy (left ventricular ejection fraction [LVEF] <= 45%) were randomized to catheter ablation (CA) or ongoing medical rate control as a pre-specified substudy of the CAMERA-MRI (Catheter Ablation versus Medical Rate Control in Atrial Fibrillation and Systolic Dysfunction-an MRIGuided Multi-centre Randomised Controlled Trial) trial. All patients had cardiac magnetic resonance imaging scans (including myocardial T1 time), serum B-type natriuretic peptide, 6-min walk tests, and Short Form-36 questionnaires performed at baseline and 6 months. Sixteen patients with no history of AF or left ventricular systolic dysfunction were enrolled as normal controls for T1 time. RESULTS Thirty-six patients (18 in each treatment arm) were included in this substudy. Demographics, comorbidities, and myocardial T1 times were well matched at baseline. At 6 months, patients in the CA group had a significant reduction in myocardial T1 time from baseline compared with the medical rate control group (-124 ms; 95% confidence interval [CI]: -23 to -225 ms; p = 0.0176), although it remained higher than that of normal controls at 6 months (p = 0.0017). Improvements in myocardial T1 time with CA were associated with significant improvements in absolute LVEF (+12.5%; 95% CI: 5.9% to 19.0%; p = 0.0004), left ventricular end-systolic volume (p = 0.0019), and serum B-type natriuretic peptide (-216 ng/ l; 95% CI: -23 to -225 ng/l; p = 0.0125). CONCLUSIONS The improvement in LVEF and reverse ventricular remodeling following successful CA of AF-mediated cardiomyopathy is accompanied by a regression of diffuse fibrosis. This suggests timely treatment of arrhythmia-mediated cardiomyopathy may minimize irreversible ventricular remodeling. (C) 2018 by the American College of Cardiology Foundation.
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