Bone manifestations in neuronopathic Gaucher disease while receiving high-dose enzyme replacement therapy

2019 ◽  
Vol 126 (2) ◽  
pp. 157-161
Author(s):  
Kunal C. Potnis ◽  
Lauren B. Flueckinger ◽  
Christine I. Ha ◽  
Jariya Upadia ◽  
Donald P. Frush ◽  
...  
Blood ◽  
1993 ◽  
Vol 82 (4) ◽  
pp. 1107-1109 ◽  
Author(s):  
A Zimran ◽  
CE Hollak ◽  
A Abrahamov ◽  
MH van Oers ◽  
M Kelly ◽  
...  

Intravenous enzyme replacement therapy (Alglucerase; Ceredase; Genzyme Corp, Boston, MA) is an effective and safe treatment for patients with type 1 Gaucher disease. In an attempt to reduce its high cost, a “low- dose high-frequency” protocol (30 U/kg/mo, 3 times a week) was introduced and found to be as effective as the original high-dose protocol (60 U/kg every 2 weeks). Because receiving frequent infusions creates a burden for many patients, we have implemented a program of home treatment for our patients. We now report the safety and feasibility of low-dose/high-frequency home intravenous enzyme- replacement therapy in 33 patients with Gaucher disease. The chronic nature of the treatment, its safety, lack of adverse effects, the stable condition of most patients, and the need to reduce the high cost make enzyme replacement for Gaucher disease a good candidate for intravenous home therapy.


Blood ◽  
1993 ◽  
Vol 82 (4) ◽  
pp. 1107-1109 ◽  
Author(s):  
A Zimran ◽  
CE Hollak ◽  
A Abrahamov ◽  
MH van Oers ◽  
M Kelly ◽  
...  

Abstract Intravenous enzyme replacement therapy (Alglucerase; Ceredase; Genzyme Corp, Boston, MA) is an effective and safe treatment for patients with type 1 Gaucher disease. In an attempt to reduce its high cost, a “low- dose high-frequency” protocol (30 U/kg/mo, 3 times a week) was introduced and found to be as effective as the original high-dose protocol (60 U/kg every 2 weeks). Because receiving frequent infusions creates a burden for many patients, we have implemented a program of home treatment for our patients. We now report the safety and feasibility of low-dose/high-frequency home intravenous enzyme- replacement therapy in 33 patients with Gaucher disease. The chronic nature of the treatment, its safety, lack of adverse effects, the stable condition of most patients, and the need to reduce the high cost make enzyme replacement for Gaucher disease a good candidate for intravenous home therapy.


2019 ◽  
Vol 22 (06) ◽  
pp. 103-117
Author(s):  
Mays Al-Tai ◽  
Deia Al-Asady ◽  
Rula Hamid

2010 ◽  
Vol 46 (4) ◽  
pp. 643-649 ◽  
Author(s):  
Maria Viviane Gomes Muller ◽  
André Petry ◽  
Luciene Pinheiro Vianna ◽  
Ana Carolina Breier ◽  
Kristiane Michelin-Tirelli ◽  
...  

Gaucher disease is a sphingolipidosis that leads to an accumulation of glucosylceramide. The objective of this study was to develop a methodology, based on the extraction, purification and quantification of glucosylceramide from blood plasma, for use in clinical research laboratories. Comparison of the glucosylceramide content in plasma from Gaucher disease patients, submitted to enzyme replacement therapy or otherwise, against that from normal individuals was also carried out. The glucosylceramide, separated from other glycosphingolipids by high performance thin layer chromatography (HPTLC) was chemically developed (CuSO4 / H3PO4) and the respective band confirmed by immunostaining (human anti-glucosylceramide antibody / peroxidase-conjugated secondary antibody). Chromatogram quantification by densitometry demonstrated that the glucosylceramide content in Gaucher disease patients was seventeen times higher than that in normal individuals, and seven times higher than that in patients on enzyme replacement therapy. The results obtained indicate that the methodology established can be used in complementary diagnosis and for treatment monitoring of Gaucher disease patients.


2014 ◽  
Vol 9 (1) ◽  
pp. 95 ◽  
Author(s):  
Marie Vigan ◽  
Jérôme Stirnemann ◽  
Catherine Caillaud ◽  
Roseline Froissart ◽  
Anne Boutten ◽  
...  

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