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法布里病患者的酶替代疗法。

Enzyme replacement therapy in patients with Fabry's disease.

作者信息

Tsuboi K

机构信息

Department of Haematology, Nagoya Central Hospital, Nagoya, Japan.

出版信息

J Int Med Res. 2007 Jul-Aug;35(4):574-81. doi: 10.1177/147323000703500418.

Abstract

Fabry's disease, a disorder affecting the gene for the lysosomal enzyme alpha-galactosidase A (alpha-GAL A), can cause accumulation of globotriaosylceramide (GL-3) in the vascular endothelial cells. Symptoms include pain, angiokeratoma, corneal clouding, and damage to the heart and kidneys. Human recombinant alpha-GAL A for use as an enzyme replacement therapy was launched in Japan in April 2004. Eleven ambulatory patients with Fabry's disease were given replacement alpha-GAL A therapy. Three patients died due to factors associated with Fabry's disease. The enzyme replacement therapies in the remaining eight patients continued safely without any notable adverse events. The following were observed: a lowering of the plasma levels of GL-3 in seven cases, an improvement in the daily activities in six cases, and a reduction in corneal clouding in three cases. Although careful observation is necessary, these results suggest that replacement alpha-GAL A therapy may be a safe and effective treatment of Fabry's disease.

摘要

法布里病是一种影响溶酶体酶α-半乳糖苷酶A(α-GAL A)基因的疾病,可导致血管内皮细胞中球三糖神经酰胺(GL-3)的蓄积。症状包括疼痛、血管角质瘤、角膜混浊以及心脏和肾脏损害。用作酶替代疗法的重组人α-GAL A于2004年4月在日本上市。11例非卧床法布里病患者接受了α-GAL A替代疗法。3例患者因与法布里病相关的因素死亡。其余8例患者的酶替代疗法安全持续,未出现任何明显不良事件。观察到以下情况:7例患者血浆GL-3水平降低,6例患者日常活动有所改善,3例患者角膜混浊减轻。尽管需要仔细观察,但这些结果表明,α-GAL A替代疗法可能是治疗法布里病的一种安全有效的方法。

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