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法布瑞病患者的肾移植和酶替代疗法。

Kidney transplantation and enzyme replacement therapy in patients with Fabry disease.

机构信息

FGM, Center of Internal Medicine, Department of Nephrology and Rheumatology, Müllheim, Germany.

出版信息

J Nephrol. 2013 Jul-Aug;26(4):645-51. doi: 10.5301/jn.5000214. Epub 2012 Sep 19.

Abstract

During Fabry disease, progressive glycosphingolipid deposition in the kidney causes gradual deterioration of renal function with proteinuria, uremia and hypertension. This results in end-stage renal disease (ESRD) which is one of the leading causes of morbidity and premature mortality in affected patients. Given the excellent graft and patient survival generally nowadays, kidney transplantation is the first choice to correct renal dysfunction and improve the overall prognosis of patients with renal failure because of Fabry disease. The benefit of enzyme-replacement therapy (ERT) in kidney transplanted Fabry patients has been controversially discussed and long-term trials focusing on the effectiveness of agalsidase in this patient population are needed.

摘要

在法布里病中,糖鞘脂在肾脏中的渐进性沉积导致肾功能逐渐恶化,出现蛋白尿、尿毒症和高血压。这会导致终末期肾脏疾病(ESRD),这是受影响患者发病率和过早死亡的主要原因之一。鉴于如今普遍出色的移植物和患者存活率,对于因法布里病而导致肾功能衰竭的患者,肾脏移植是纠正肾功能障碍和改善整体预后的首选方法。在接受过肾脏移植的法布里病患者中,酶替代疗法(ERT)的益处存在争议,需要进行长期试验来关注阿加糖酶在这一患者群体中的有效性。

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