Abstract

The clinical features, CMR characteristics and outcomes of arrhythmogenic left ventricular cardiomyopathy (ALVC), which is a very rare nonischemic cardiomyopathy, are currently not well studied. The purpose of the study is to investigate the clinical and cardiovascular magnetic resonance (CMR) imaging characteristics of arrhythmogenic left ventricular cardiomyopathy (ALVC). Fifty-three consecutive patients with ALVC were divided into two groups: ALVC patients without right ventricular (RV) involvement (n = 36, group 1) and those with RV involvement (n = 17, group 2). Clinical symptoms, cardiac electrophysiological findings, and CMR parameters (morphology, ventricular function, and myocardial fibrosis and fatty infiltration) were evaluated in both groups. The two groups showed no significant difference in age, gender, or presenting symptoms (P > 0.05). Right bundle branch block ventricular arrhythmia was less common in patients without RV involvement (50.0% vs.64.7%, P = 0.031). There were no significant differences in left ventricular function between the two groups, however right ventricular ejection fraction was significantly lower in group 2 (40.1 ± 4.0% vs. 48.7 ± 3.9%, P < 0.001). Inverse correlations of left ventricular ejection fraction with fat volume (r = −0.883, p = 0.001), late gadolinium enhancement (LGE) volume (r = −0.892, 0.013), ratio of fat/LGE (r = −0.848, p < 0.001), indexed left ventricular end diastolic volume (r = −0.877, p < 0.001) and indexed left ventricular end systolic volume (r = −0.943, p < 0.001) were all significant. ALVC is a rare disease with fibro-fatty replacement predominantly in the left ventricle, impaired left ventricular systolic function, and ventricular arrhythmias originating from the left ventricle. ALVC with right ventricular involvement may have a worse prognosis.

Highlights

  • Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare cardiomyopathy with a prevalence of 1/1000 to 1/50001

  • We hope to improve the clinical awareness of this disease, which will be referred to as arrhythmogenic left ventricular cardiomyopathy (ALVC) in this manuscript, and to provide information that will aid in both clinical decision making and further management of this group of patientss

  • With the exception of RV ejection fraction (RVEF) and RV end-systolic volume index (RVESVI), there was no significant difference between the two groups with regards to functional parameters

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Summary

Introduction

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare cardiomyopathy with a prevalence of 1/1000 to 1/50001. Imaging modalities usually reveal severe LV dysfunction with preserved to mildly impaired RV function Often this entity has been misdiagnosed as dilated cardiomyopathy, chronic myocarditis, myocardial infarction, or double ventricular involvement type ARVC12,13. We hope to improve the clinical awareness of this disease, which will be referred to as arrhythmogenic left ventricular cardiomyopathy (ALVC) in this manuscript, and to provide information that will aid in both clinical decision making and further management of this group of patientss

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