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胱氨酸贮积症肾病患者血浆 chitotriosidase 活性

Chitotriosidase plasma activity in nephropathic cystinosis.

机构信息

First Department Pediatrics, Athens University, Athens, Greece.

出版信息

J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S157-9. doi: 10.1007/s10545-009-1118-8. Epub 2009 May 20.

Abstract

Chitotriosidase is a fully active chitinase produced and secreted by activated phagocytes. Plasma chitotriosidase activity is a well-established marker of total disease burden in Gaucher disease that has proved useful in monitoring the response to both enzyme replacement and substrate reduction therapies in patients with Gaucher disease. Increased chitotriosidase plasma activity has also been observed in several other lysosomal and non lysosomal disorders. Cystinosis, a rare multisystemic lysosomal storage disease, is characterized by the intralysosomal accumulation of free cystine in many cell types including phagocytes. We here report on plasma chitotriosidase activity in a child with nephropathic cystinosis. Increased plasma chitotriosidase activity (481 nmol/h per ml; normal range 0-150 units) was found on diagnosis and prior to the initiation of oral cysteamine (Cystagon) treatment. Serial estimations of plasma chitotriosidase activity showed that it correlated with leukocyte cystine content and decreased to 100 nmol/h per ml following 14 months' treatment. This novel observation suggests that cystinosis should be included in the differential diagnosis of disorders associated with increased plasma chitotriosidase activity. Furthermore, it suggests that serial estimations of plasma chitotriosidase activity could be of value in monitoring the response to oral cysteamine treatment in cystinosis.

摘要

几丁质酶是一种由活化的吞噬细胞产生和分泌的完全活性的几丁质酶。血浆几丁质酶活性是戈谢氏病总疾病负担的一个既定标志物,已被证明在监测戈谢氏病患者对酶替代和底物减少治疗的反应方面非常有用。在几种其他溶酶体和非溶酶体疾病中也观察到增加的血浆几丁质酶活性。胱氨酸贮积症是一种罕见的多系统溶酶体贮积病,其特征是许多细胞类型(包括吞噬细胞)内溶酶体中游离胱氨酸的积累。我们在此报告一例肾性胱氨酸贮积症患儿的血浆几丁质酶活性。在诊断时和开始口服半胱氨酸(Cystagon)治疗之前,发现血浆几丁质酶活性增加(481 nmol/h 每毫升;正常范围 0-150 单位)。对血浆几丁质酶活性的连续评估表明,它与白细胞胱氨酸含量相关,并在 14 个月的治疗后降至 100 nmol/h 每毫升。这一新的观察结果表明,胱氨酸贮积症应包括在与血浆几丁质酶活性增加相关的疾病的鉴别诊断中。此外,它表明血浆几丁质酶活性的连续评估可能对监测胱氨酸贮积症患者口服半胱氨酸治疗的反应有价值。

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