Key result
Endovascular severe mitral regurgitation induction drives a ~160% increase in left atrial volume.
Why the study?
To develop a minimally invasive, reproducible model of chronic severe mitral regurgitation replicating left atrial and left ventricular dilation and susceptibility to atrial fibrillation.
Does endovascular chordae avulsion create a reproducible model of chronic severe mitral regurgitation with structural and electrophysiologic remodeling in dogs?
Does endovascular chordae avulsion create a reproducible model of chronic severe mitral regurgitation with structural and electrophysiologic remodeling in dogs?
Absolute Event Rate: 56% vs 21.6%
p-value: p=0.039
This minimally invasive canine model successfully replicates the clinical phenotype of severe mitral regurgitation, demonstrating marked left atrial and ventricular remodeling and increased susceptibility to atrial tachyarrhythmias.
Supports a reproducible canine model of MR-induced remodeling and arrhythmias; leaves open translation to human therapies.
ObjectiveTo develop a minimally invasive, reproducible model of chronic severe mitral regurgitation (MR) that replicates the clinical phenotype of left atrial (LA) and left ventricular dilation and susceptibility to atrial fibrillation.MethodsUnder transesophageal echocardiographic guidance, chordae tendinae were avulsed using endovascular forceps until the ratio of regurgitant jet area to LA area was ≥70%. Animals survived for an average of 8.6 ± 1.6 months (standard deviation) and imaged with monthly transthoracic echocardiography (TTE). Animals underwent baseline and preterminal magnetic resonance imaging. Terminal studies included TTE, transesophageal echocardiography, and rapid atrial pacing to test inducibility of atrial tachyarrhythmias.ResultsEight dogs underwent creation of severe MR and interval monitoring. Two were excluded—one died from acute heart failure, and the other had resolution of MR. Six dogs underwent the full experimental protocol; only one required medical management of clinical heart failure. MR remained severe over time, with a mean terminal regurgitant jet area to LA area of 71 ± 14% (standard deviation) and regurgitant fraction of 52 ± 11%. Mean LA volume increased over 130% (TTE: 163 ± 147%, P = .039; magnetic resonance imaging: 132 ± 54%, P = .011). Mean left ventricular end-diastolic volume increased by 38 ± 21% (P = .008). Inducible atrial tachyarrhythmias were seen in 4 of 6 animals at terminal surgery, and none at baseline.ConclusionsWithin the 6 dogs that successfully completed the full experimental protocol, this model replicated the clinical phenotype of severe MR, which led to marked structural and electrophysiologic cardiac remodeling. This model allowed for precise measurements at repeated time points and will facilitate future studies to elucidate the mechanisms of atrial and ventricular remodeling secondary to MR and the pathophysiology of valvular atrial fibrillation.
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McGilvray et al. (2023) studied Chronic severe mitral regurgitation (n=6). Endovascular avulsion of mitral valve chordae tendinae vs. Baseline was evaluated on Indexed left atrial volume (mL) via transthoracic echocardiography (p=0.039). Endovascular creation of severe mitral regurgitation in a canine model resulted in a 163% increase in left atrial volume and inducible atrial tachyarrhythmias in 67% of animals after 9 months.
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