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Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III

BACKGROUND: Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is caused by a deficiency in one of the four enzymes involved in the lysosomal degradation of heparan sulfate. Cardiac abnormalities have been observed in patients with all types of MPS except MPS IX, however few studies h...

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Autores principales: Lin, Hsiang-Yu, Chen, Ming-Ren, Lin, Shan-Miao, Hung, Chung-Lieh, Niu, Dau-Ming, Chang, Tung-Ming, Chuang, Chih-Kuang, Lin, Shuan-Pei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567572/
https://www.ncbi.nlm.nih.gov/pubmed/31196149
http://dx.doi.org/10.1186/s13023-019-1112-7
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author Lin, Hsiang-Yu
Chen, Ming-Ren
Lin, Shan-Miao
Hung, Chung-Lieh
Niu, Dau-Ming
Chang, Tung-Ming
Chuang, Chih-Kuang
Lin, Shuan-Pei
author_facet Lin, Hsiang-Yu
Chen, Ming-Ren
Lin, Shan-Miao
Hung, Chung-Lieh
Niu, Dau-Ming
Chang, Tung-Ming
Chuang, Chih-Kuang
Lin, Shuan-Pei
author_sort Lin, Hsiang-Yu
collection PubMed
description BACKGROUND: Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is caused by a deficiency in one of the four enzymes involved in the lysosomal degradation of heparan sulfate. Cardiac abnormalities have been observed in patients with all types of MPS except MPS IX, however few studies have focused on cardiac alterations in patients with MPS III. METHODS: We reviewed medical records, echocardiograms, and electrocardiograms of 26 Taiwanese patients with MPS III (five with IIIA, 20 with IIIB, and one with IIIC; 14 males and 12 females; median age, 7.4 years; age range, 1.8–26.5 years). The relationships between age and each echocardiographic parameter were analyzed. RESULTS: Echocardiographic examinations (n = 26) revealed that 10 patients (38%) had valvular heart disease. Four (15%) and eight (31%) patients had valvular stenosis or regurgitation, respectively. The most prevalent cardiac valve abnormality was mitral regurgitation (31%), followed by aortic regurgitation (19%). However, most of the cases of valvular heart disease were mild. Three (12%), five (19%) and five (19%) patients had mitral valve prolapse, a thickened interventricular septum, and asymmetric septal hypertrophy, respectively. The severity of aortic regurgitation and the existence of valvular heart disease, aortic valve abnormalities and valvular stenosis were all positively correlated with increasing age (p < 0.05). Z scores > 2 were identified in 0, 38, 8, and 27% of left ventricular mass index, interventricular septal end-diastolic dimension, left ventricular posterior wall end-diastolic dimension, and aortic diameter, respectively. Electrocardiograms in 11 patients revealed the presence of sinus arrhythmia (n = 3), sinus bradycardia (n = 2), and sinus tachycardia (n = 1). Six patients with MPS IIIB had follow-up echocardiographic data at 1.9–18.1 years to compare with the baseline data, which showed some patients had increased thickness of the interventricular septum, as well as more patients had valvular abnormalities at follow-up. CONCLUSIONS: Cardiac involvement in MPS III is less common and milder compared with other types of MPS. The existence of valvular heart disease, aortic valve abnormalities and valvular stenosis in the patients worsened with increasing age, reinforcing the concept of the progressive nature of this disease.
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spelling pubmed-65675722019-06-17 Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III Lin, Hsiang-Yu Chen, Ming-Ren Lin, Shan-Miao Hung, Chung-Lieh Niu, Dau-Ming Chang, Tung-Ming Chuang, Chih-Kuang Lin, Shuan-Pei Orphanet J Rare Dis Research BACKGROUND: Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is caused by a deficiency in one of the four enzymes involved in the lysosomal degradation of heparan sulfate. Cardiac abnormalities have been observed in patients with all types of MPS except MPS IX, however few studies have focused on cardiac alterations in patients with MPS III. METHODS: We reviewed medical records, echocardiograms, and electrocardiograms of 26 Taiwanese patients with MPS III (five with IIIA, 20 with IIIB, and one with IIIC; 14 males and 12 females; median age, 7.4 years; age range, 1.8–26.5 years). The relationships between age and each echocardiographic parameter were analyzed. RESULTS: Echocardiographic examinations (n = 26) revealed that 10 patients (38%) had valvular heart disease. Four (15%) and eight (31%) patients had valvular stenosis or regurgitation, respectively. The most prevalent cardiac valve abnormality was mitral regurgitation (31%), followed by aortic regurgitation (19%). However, most of the cases of valvular heart disease were mild. Three (12%), five (19%) and five (19%) patients had mitral valve prolapse, a thickened interventricular septum, and asymmetric septal hypertrophy, respectively. The severity of aortic regurgitation and the existence of valvular heart disease, aortic valve abnormalities and valvular stenosis were all positively correlated with increasing age (p < 0.05). Z scores > 2 were identified in 0, 38, 8, and 27% of left ventricular mass index, interventricular septal end-diastolic dimension, left ventricular posterior wall end-diastolic dimension, and aortic diameter, respectively. Electrocardiograms in 11 patients revealed the presence of sinus arrhythmia (n = 3), sinus bradycardia (n = 2), and sinus tachycardia (n = 1). Six patients with MPS IIIB had follow-up echocardiographic data at 1.9–18.1 years to compare with the baseline data, which showed some patients had increased thickness of the interventricular septum, as well as more patients had valvular abnormalities at follow-up. CONCLUSIONS: Cardiac involvement in MPS III is less common and milder compared with other types of MPS. The existence of valvular heart disease, aortic valve abnormalities and valvular stenosis in the patients worsened with increasing age, reinforcing the concept of the progressive nature of this disease. BioMed Central 2019-06-13 /pmc/articles/PMC6567572/ /pubmed/31196149 http://dx.doi.org/10.1186/s13023-019-1112-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lin, Hsiang-Yu
Chen, Ming-Ren
Lin, Shan-Miao
Hung, Chung-Lieh
Niu, Dau-Ming
Chang, Tung-Ming
Chuang, Chih-Kuang
Lin, Shuan-Pei
Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
title Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
title_full Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
title_fullStr Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
title_full_unstemmed Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
title_short Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
title_sort cardiac characteristics and natural progression in taiwanese patients with mucopolysaccharidosis iii
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567572/
https://www.ncbi.nlm.nih.gov/pubmed/31196149
http://dx.doi.org/10.1186/s13023-019-1112-7
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