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DOI 10.1016/j.ymgme.2016.02.003

Медицинская библиотека · Molecular genetics and metabolism · 2016

Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VI.

Lin Hsiang-Yu, Chuang Chih-Kuang, Chen Ming-Ren, Lin Shan-Miao, Hung Chung-Lieh, Chang Chia-Ying, Chiu Pao Chin, Tsai Wen-Hui, Niu Dau-Ming, Tsai Fuu-Jen, Lin Shio Jean, Hwu Wuh-Liang, Lin Ju-Li, Lin Shuan-Pei

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

While enzyme replacement therapy (ERT) has been shown to improve endurance and joint mobility for patients with mucopolysaccharidoses (MPS) I, II, IVA and VI, the impact of ERT on cardiac abnormalities remains uncertain.

METHODS

Medical records and echocardiograms of 28 Taiwanese MPS patients (9 with MPS I, 7 with MPS II, 7 with MPS IVA, and 5 with MPS VI) treated with ERT for 1-10.8years were retrospectively reviewed.

RESULTS

At start of ERT, z scores>2 were identified in 46% and 75% for left ventricular mass index (LVMI) and interventricular septum thickness in diastole (IVSd) in these patients, respectively. Twenty-four patients (86%) had valvular heart disease. After ERT, the mean IVSd z score of all patients decreased significantly from 3.87 to 2.57 (p=0.016). For 11 patients starting ERT before 12years of age, z scores for both LVMI and IVSd decreased significantly (p<0.01) after ERT. However, the condition of valve regurgitation or stenosis did not show improvement despite ERT.

CONCLUSIONS

ERT was shown to be an effective therapy for reducing cardiac hypertrophy, with best results seen when ERT was started at an early age. ERT, however, had little impact on valvular heart disease.

Для цитирования: Lin Hsiang-Yu, Chuang Chih-Kuang, Chen Ming-Ren, Lin Shan-Miao, Hung Chung-Lieh, Chang Chia-Ying, Chiu Pao Chin, Tsai Wen-Hui, Niu Dau-Ming, Tsai Fuu-Jen, Lin Shio Jean, Hwu Wuh-Liang, Lin Ju-Li, Lin Shuan-Pei. Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VI.. Molecular genetics and metabolism. 2016. DOI: 10.1016/j.ymgme.2016.02.003.

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