Abstract

BackgroundCardiac abnormalities have been observed in patients with mucopolysaccharidosis type II (MPS II). The aim of this study was to investigate the cardiac features and natural progression of Taiwanese patients with MPS II, and evaluate the impact of enzyme replacement therapy (ERT) on cardiac structure and function.MethodsThe medical records and echocardiograms of 48 Taiwanese patients with MPS II (median age, 6.9 years; age range, 0.1–27.9 years) were reviewed. The relationships between age and each echocardiographic parameter were analyzed.ResultsThe mean z-scores of left ventricular mass index (LVMI), interventricular septum diameter in diastole (IVSd), left ventricular posterior wall diameter in diastole (LVPWd), and aortic diameter were 1.10, 2.70, 0.95 and 1.91, respectively. Z scores > 2 were identified in 33%, 54%, 13%, and 46% for LVMI, IVSd, LVPWd, and aortic diameter, respectively. The most prevalent cardiac valve abnormality was mitral regurgitation (MR) (56%), followed by aortic regurgitation (AR) (33%). The severity of mitral stenosis (MS), MR, aortic stenosis (AS), AR, and the existence of valvular heart disease were all positively correlated with increasing age (p < 0.01). We also compared the echocardiographic parameters between two groups: (1) 12 patients who had up to 17 years of follow-up echocardiographic data without ERT, and (2) nine patients who had up to 12 years of follow-up data with ERT. The results showed that z-score changes of LVMI significantly improved in the patients who received ERT compared to those who did not receive ERT (0.05 versus 1.52, p < 0.05). However, the severity score changes of MS, MR, AS, and AR all showed gradual progression in both groups (p > 0.05).ConclusionsHigh prevalence rates of valvular heart disease and cardiac hypertrophy were observed in the MPS II patients in this study. The existence and severity of cardiac hypertrophy and valvular heart disease in these patients worsened with increasing age, reinforcing the concept of the progressive nature of this disease. ERT for MPS II appeared to be effective in stabilizing or reducing the progression of cardiac hypertrophy, but it only had a limited effect on valvulopathy.

Highlights

  • Mucopolysaccharidoses (MPSs; OMIM 252700) are a group of lysosomal storage diseases caused by deficiencies in specific lysosomal enzymes that involve the sequential catabolism of glycosaminoglycans (GAGs) leading to progressive substrate accumulation in various tissues and organs

  • There were 24 neuronopathic and 24 non-neuronopathic patients in this study. Most of these patients (n = 41, 85%) had cardiac abnormalities, and only seven who were referred from newborn screening programs (Patients No 1, 2, 4–6, 12, 23) had normal cardiac features by echocardiography

  • Z-scores for left ventricular mass index (LVMI), interventricular septal end-diastolic dimension (IVSd) and left ventricular posterior wall diameter in diastole (LVPWd) were all positively correlated with increasing age (p < 0.05) (Table 3 and Fig. 1)

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Summary

Introduction

Mucopolysaccharidoses (MPSs; OMIM 252700) are a group of lysosomal storage diseases caused by deficiencies in specific lysosomal enzymes that involve the sequential catabolism of glycosaminoglycans (GAGs) leading to progressive substrate accumulation in various tissues and organs. Seven different types of MPS disorders (I, II, III, IV, VI, VII, and IX) with 11 specific lysosomal enzyme deficiencies have been reported. MPS II (Hunter syndrome; OMIM +309900) is an inherited X-linked recessive disease caused by deficient activity of iduronate-2-sulfatase (IDS), which catalyzes a sequential step in the degradation of the GAGs dermatan sulfate and heparan sulfate. Patients with the severe form of MPS II usually manifest between 2 and 4 years of age with coarse face, recurrent ear, nose, and throat infections, airway obstruction, cardiac valve dysplasia, cardiomyopathy, hepatosplenomegaly, hernias, skeletal deformities, joint stiffness, and progressive neurological deterioration, leading to profound cognitive impairment. The aim of this study was to investigate the cardiac features and natural progression of Taiwanese patients with MPS II, and evaluate the impact of enzyme replacement therapy (ERT) on cardiac structure and function

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