Abstract

PurposeTo determine whether 3.0-T magnetic resonance imaging (MRI) could assess right ventricular (RV) function in patients with hypertrophic cardiomyopathy (HCM), and if this assessment is correlated with the New York Heart Function Assessment (NYHA) classification.Materials and MethodsForty-six patients with HCM and 23 normal individuals were recruited. Left and right ventricular function parameters including end-diastolic and end-systolic volumes (EDV, ESV), stroke volume (SV) and ejection fraction (EF) and dimensions were measured and compared using 3.0-T MRI. RV function parameters between HCM patients and controls were compared using independent sample t tests. A one way ANOVA test with Bonferroni correction was used to determine significant differences among different NYHA groups. Receiver operating characteristic analyses calculated the sensitivity and specificity of RV dysfunction on MRI for the prediction of HCM severity.ResultsStatistical analysis revealed significant differences of left ventricular (LV) and RV volumetric values and masses between the HCM patients and controls (all p<0.05). Within the HCM group, the simultaneously decreased maximum RVEDD correlated well with the LVEDD (r = 0.53; p<0.001). The function and dimension parameters among Class I to III were not determined to be significantly different (all p>0.05). However, significant differences between the Class IV and I-III groups (all P<0.0167) indicated that the diastolic and systolic function in both the RV and LV were impaired in Class IV patients. ROC analyses identified the EDV, ESV and EDD of both the LV and RV with a high sensitivity cutoff value to predict the HCM patients with severe heart failure (Class IV) with high sensitivity and specificity.ConclusionsRV involvements were comparable to those of LV global function impairments in patients with HCM. The presence of RV dysfunction and decreased dimension on the MRI helped to predict the severe symptomatic HCM with high sensitivity and specificity.

Highlights

  • Hypertrophic cardiomyopathy (HCM) is the most prevalent, heritable cardiovascular disease with a prevalence rate of 1 in 500 [1]

  • Significant differences between the Class IV and I-III groups indicated that the diastolic and systolic function in both the right ventricular (RV) and left ventricular (LV) were impaired in Class IV patients

  • Significant differences between the Class IV and I–III groups indicated that thediastolic and systolic function in both the RV and LV were impaired in Class IV patients

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Summary

Introduction

Hypertrophic cardiomyopathy (HCM) is the most prevalent, heritable cardiovascular disease with a prevalence rate of 1 in 500 [1]. Most clinical evaluations focus on LV function, ignoring the right ventricular (RV) function [3,4]. We evaluated the regional myocardial microvascular dysfunction differences in hypertrophic cardiomyopathy (HCM) patients with or without LV outflow tract obstruction with first-pass perfusion CMR imaging [5]. RV dysfunction is of interest as a strong indicator of cardiovascular morbidity and mortality in patients with heart failure. Right heart failure may be caused by chronic pressure overload that is prone to be ignored for prolonged periods [6,7,8]. The evaluation of RV dysfunction is necessary in patients with HCM

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