Serum chitotriosidase activity in Gaucher patients on enzyme replacement therapy (ERT)

被引:22
|
作者
Czartoryska, B
Tylki-Szymanska, A
Górska, D
机构
[1] Inst Psychiat & Neurol, Dept Genet, PL-02057 Warsaw, Poland
[2] Childrens Mem Hlth Inst, Dept Metab Dis, PL-02957 Warsaw, Poland
关键词
chitotriosidase; Gaucher; Ceredase (R); enzyme replacement therapy (ERT);
D O I
10.1016/S0009-9120(98)00030-7
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objective: Changes of serum chitotriosidase activity during Ceredase(R) treatment of Gaucher patients. Design and Methods: Ten Gaucher patients were treated with Ceredase for up to 30 months. Serum or plasma chitotriosidase activity was measured using 4-methylumbelliferyl-beta-D-N, N',N" triacetyl-chitotrioside. Results: In untreated patients, serum chitotriosidase activity did not depend on the patient's age and was not a measure of clinical status, type or progress of the disease. Chitotriosidase activity declined during treatment with Ceredase, but still remained high. The largest decline in enzyme activity was observed in patients with type III of the disease who had intact spleens; splenectomized type III patients, and type I patients reacted more slowly. Conclusions: Serum chitotriosidase activity may indicate that a patient has reacted to treatment, however, it can not be considered a direct marker of treatment effectiveness. Copyright (C) 1998 The Canadian Society of Clinical Chemists.
引用
收藏
页码:417 / 420
页数:4
相关论文
共 50 条
  • [21] Enzyme replacement therapy (ERT) in pompe disease
    Fiumara A.
    Italian Journal of Pediatrics, 40 (Suppl 1) : 1 - 1
  • [22] Ambroxol therapy for patients with Gaucher disease type 1, either poor responders to enzyme replacement therapy/substrate reduction therapy (ERT/SRT) or untreated
    Istaiti, Majdolen J.
    Becker-Cohen, Michal
    Frydman, Dafna
    Dinur, Tama
    Revel-Vilk, Shoshana
    Zimran, Ari
    MOLECULAR GENETICS AND METABOLISM, 2023, 138 (02) : 66 - 66
  • [23] Gaucher disease and enzyme replacement therapy in patients of northern Greece
    Gombakis, N.
    Vargiami, E.
    Michelakaki, E.
    Dimitriou, E.
    Moraitou, M.
    Tsantali, C.
    Athanasiou-Metaxa, M.
    Zafeiriou, D. I.
    CLINICAL THERAPEUTICS, 2007, 29 : S118 - S119
  • [24] Enzyme replacement therapy with imiglucerase in Indian patients with Gaucher disease
    Gupta, Neerja
    Kabra, Madhulika
    Shrivastava, Ranjana
    Vashist, Suman
    MOLECULAR GENETICS AND METABOLISM, 2009, 96 (02) : S26 - S26
  • [25] Renal function in patients with fabry disease on enzyme replacement therapy (ERT)
    West, Michael
    Cybulla, Markus
    Feriozzi, Sandro
    Schwarting, Andreas
    Schiffmann, Raphael
    Mehta, Atul
    Sunder-Plassmann, Gere
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2007, 22 : 13 - 13
  • [26] ENZYME-REPLACEMENT THERAPY (ERT) IN MPS PATIENTS WITH CNS MANIFESTATION
    Lampe, C.
    Miebach, E.
    Kraemer, E.
    Beck, M.
    MOLECULAR GENETICS AND METABOLISM, 2009, 98 (1-2) : 64 - 64
  • [27] Population pharmacokinetic of enzymatic activity of glucocerebrosidase in Gaucher disease patients treated with enzyme replacement therapy
    Gras-Colomer, Elena
    Mangas-Sanjuan, Victor
    Climente-Marti, Monica
    Merino-Sanjuan, Matilde
    MOLECULAR GENETICS AND METABOLISM, 2020, 129 (02) : S68 - S68
  • [28] The Gaucher Registry: Demographics and disease characteristics of 996 patients (PTS) on enzyme replacement therapy (ERT) compared to 438 untreated PTS.
    Weinreb, N
    Andersson, H
    Charrow, J
    Kaplan, P
    Kolodny, E
    Mistry, P
    Pastores, G
    Rosenbloom, B
    Scott, CR
    Wappner, R
    Zimran, A
    BLOOD, 1999, 94 (10) : 211A - 211A
  • [29] Clinical factors influencing the achievement of a complete response (CR) after 24 months of enzyme replacement therapy (ERT) in patients with Gaucher disease (GD): The Gaucher Registry.
    Weinreb, NJ
    Andersson, HC
    Charrow, J
    Kaplan, P
    Kolodny, EH
    Mistry, P
    Pastores, G
    Rosenbloom, BE
    Scott, CR
    Wappner, RS
    BLOOD, 2001, 98 (11) : 20A - 20A
  • [30] Value of plasma chitotriosidase to assess non-neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapy
    van Dussen, L.
    Hendriks, E. J.
    Groener, J. E. M.
    Boot, R. G.
    Hollak, C. E. M.
    Aerts, J. M. F. G.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2014, 37 (06) : 991 - 1001