Outcome of Gaucher Disease in India: Lessons from Prevalent Diagnostic and Therapeutic Practices

被引:4
|
作者
Muranjan, Mamta
Patil, Smita
机构
[1] Seth GS Med Coll, Dept Pediat, Genet Clin, Bombay, Maharashtra, India
[2] King Edward Mem Hosp, Bombay, Maharashtra, India
关键词
Glucocerebrosidase deficiency; GBA; 1; gene; lysosomal storage disease; ENZYME REPLACEMENT THERAPY; RECOMMENDATIONS; SEVERITY; CHILDREN; TYPE-1;
D O I
10.1007/s13312-016-0910-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives: To study disease severity and response to enzyme replacement therapy in Gaucher disease. Methods: Updated data was captured from records of 37 patients (35 reported previously) with confirmed diagnosis of Gaucher disease from January 1995 through December 2011 (31, 83.8 %) and prospectively from January 2012 through June 2013 (6, 16.2 %). Severity of manifestations was determined by Gaucher disease Severity Score Index. Response to enzyme replacement therapy was assessed in terms of attainment of therapeutic goals. Results: Moderate to severe manifestations (domain score of > 2) were observed in treated patients at baseline (83%, 58%, 66% and 25% for anemia, thrombocytopenia, hepatomegaly and leucopenia, respectively and 100% for splenomegaly and elevated plasma chitotriosidase). None of the 11 patients treated with synthetic enzyme (average annual dose 23 to 53 units/kg) attained all therapeutic goals in the recommended time frame, particularly the visceral, skeletal and growth domains. Conclusions: Early onset of moderate to severe disease in Indian patients mandates early therapy with optimum doses to ensure attainment of all recommended therapeutic goals.
引用
收藏
页码:685 / 688
页数:4
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